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Pre-filled Syringes West Coast (Virtual Conference)
June 14 - June 15, 2021

Post event on demand access to recorded presentations will be available to all attendees 5 working days from the end date of the event.

Pre-filled Syringes West Coast (Virtual Conference)

SAE Media Group is proud to present the 5th Annual Pre-Filled Syringes West Coast Virtual Conference on 14th and 15th June 2021 | ALL TIMINGS ARE PDT
 

Following the success of the last event, the Pre-Filled Syringes West Coast conference is back to uncover the latest innovations in combination product development, device design, human factors engineering and drug product formulation to give a holistic overview of the industry and what we can expect for the future.


With the global market for prefilled syringes estimated to exceed $9.7bn by 2025, this year’s agenda will encompass key drivers and hot topics of the industry including; updates to regulatory guidance from industry experts and regulatory bodies, case studies on device design and complex formulation, life cycle and control strategies, and innovations in connectivity and digital health.
 

This two-day agenda offers you peer-to-peer networking with Global Product Managers, Senior PFS Engineers, Device Testing Managers, Heads of Late-Stage PFS Development and many more.
 

We look forward to welcoming you to the conference in June.
 

This is one of our most sought-after event and will be sold out soon.
 

Early registration is strongly advised to avoid disappointment.
 

FEATURED SPEAKERS

Aly McDonald

Aly McDonald

Human Factors Engineer, Genentech
Amin Sedighiamiri

Amin Sedighiamiri

Engineering Manager, Device Development, AstraZeneca
Darin Zehrung

Darin Zehrung

Global Program Leader , PATH
Jace  Blackburn

Jace Blackburn

Smart Device Engineer, Genentech
James Wabby

James Wabby

Executive Director, Head of Regulatory Strategy, Emerging Technologies and Combination Products, AbbVie
Khaudeja Bano

Khaudeja Bano

Executive Medical Director, Combination Product Safety Head, Amgen
Larry Atupem

Larry Atupem

Sr Business Development Specialist, Zeon Specialty Materials
Mark DeStefano

Mark DeStefano

Director CPD – Feasibility, New Technology and Prototyping Development, Teva Pharmaceuticals
Miles Buroker

Miles Buroker

Human Factors Engineer, UserWise, Inc.
Natalie Abts

Natalie Abts

Head of Human Factors Engineering, Genentech
Patricia Hojnoski

Patricia Hojnoski

Associate Director, Janssen (Johnson & Johnson)
Sarah Mollo

Sarah Mollo

Combination Product Policy Analyst, Food and Drug Administration
Severine Duband

Severine Duband

Category Director, Devices, Nemera
Shannon Clark

Shannon Clark

CEO, UserWise, Inc.
Takuya Minezaki

Takuya Minezaki

Research Manager, Mitsubishi Gas Chemical Company, Inc.
Tina Rees

Tina Rees

Associate Director, Regeneron Pharmaceuticals
Tracy Hsu

Tracy Hsu

Senior Director, CMC Program Management, Alexion Pharmaceuticals, Inc

Aly McDonald

Human Factors Engineer, Genentech
Aly McDonald

Aly is a Human Factors Engineer at Genentech, where she acts as the primary HF representative on several project teams, including a digital health program, a novel drug-device platform, a non-combination product project, and multiple late stage drug-device combination product programs. She has experience conducting human factors activities from early-stage research through design validation. Prior to joining the Human Factors team, Aly held various roles within Pharma Technical Operations at Genentech.

Amin Sedighiamiri

Engineering Manager, Device Development, AstraZeneca
Amin Sedighiamiri

Amin Sedighiamiri has a PhD in Mechanical Engineering with more than 12 years of technical leadership experience, including product innovation and commercialization across multiple industry segments, like medical device, combination product, automotive and water management in Europe and the US. Currently, he is Device Development Engineering Manager in Dosage Form Design and Development organization of AstraZeneca where he is leading combination product development as well as smart drug delivery device technology development projects.

Before joining AstraZeneca, Amin worked as Sr. Engineer in Delivery, Device and Connected Solutions Organization of Eli Lilly and Company, where he led cross-functional teams of engineers to develop connected solutions for drug delivery devices.

He is also Board Member and Technical Programming Committee Chair at Medical Plastics Division in Society of Plastics Engineers.
 

Darin Zehrung

Global Program Leader , PATH
Darin Zehrung

Darin Zehrung, MBA, leads PATH’s Medical Devices and Health Technologies Program. Mr. Zehrung also serves on the leadership team for PATH’s Center for Vaccine Innovation and Access and serves as co-chair of the World Health Organization’s Immunization Practices Advisory Committee Delivery Technologies Working Group.

Mr. Zehrung previously led PATH’s portfolio in vaccine and pharmaceutical delivery technologies, helping position PATH as a globally recognized expert in delivery and packaging technologies for vaccines and essential medicines. He also led the work to establish a Center of Excellence at PATH for microarray patches and serves as the director.
 

Jace Blackburn

Smart Device Engineer, Genentech
Jace  Blackburn

Jace Blackburn is a Smart Device Engineer at Genentech where he oversees development of Connected Device Platforms to improve the patient experience and enable new digital strategies for the business. He holds a degree in Chemical and Biological Engineering from the University of Colorado Boulder and is currently pursuing a Masters in Bioinformatics from Johns Hopkins. He holds multiple certifications in Product Management and brings expertise on the development of software as a medical devices, connected devices, and digital combination products.

James Wabby

Executive Director, Head of Regulatory Strategy, Emerging Technologies and Combination Products, AbbVie
James Wabby

Over 15 years of experience in increasing quality compliance and regulatory affairs responsibilities within the GxP regulated environment pertaining to Nutritional, Cosmetic, Branded Pharmaceutical, Generic, Biologic, Medical Device and Combination Product areas.

Regularly provides Allergan therapeutic franchise units regulatory counsel to all aspects within the quality management system arena pertaining to medical devices and combination products regarding:

• Regulatory Affairs – CMC Global Dossiers and Device Regulatory Strategy Registrations
• MDR/IVDR – Person Responsible for Regulatory Compliance
• ISO 13485:2016/MDSAP
• Product Development – Design Controls
• Risk Management
• Human Factors Engineering
• Acquisitions/Divestitures
• Import/Export – U.S. Agent
• CAPA
• Production Controls
• Regulatory Inspection Management
• Materiovigilance
• Health-Care Related Laws and International Regulations

 

 


Education


2000 – BSc., Biology, Duquesne University
2002 – MHMS, Health Law/Policy and Medical Informatics, Duquesne University
2011 - Certificate, Health Care Compliance Certificate, Seton Hall University Law School

Industry

Member of various regulatory and quality work groups including DIA, RAPS, AAMI, AHLA and the ASQ Orange Empire Section.
 

Khaudeja Bano

Executive Medical Director, Combination Product Safety Head, Amgen
Khaudeja Bano

Khaudeja is a Physician with a Masters in Clinical Research, Pharmaceutical engineering Certification, a Database Administrator and a certified Project Management Professional.

She is an Abbott President’s award winner, avid Toastmaster and Coach. Khaudeja has more than 25 years’ professional experience, including clinical practice. She has held several global medical positions at Guidant, Abbott, and AbbVie Inc. Her career includes global medical / clinical and safety leadership roles in devices, diagnostics, pharmaceuticals and combination products.

She currently serves as the chair for the Post Marketing Safety working group for the Combination Product Coalition (CPC).

Larry Atupem

Sr Business Development Specialist, Zeon Specialty Materials
Larry Atupem

Larry Atupem is the Sr. Business development specialist at Zeon Specialty materials with responsibility for development and marketing of Cyclic Olefin Polymer business in North America. He has over decade of experience in multiple industries spanning from pharmaceutical science, thermal packaging, and thermoplastics. He holds a Bachelor of Science degree in Chemical & Biological Engineering from Tufts University along with management business coursework from Boston University.

Mark DeStefano

Director CPD – Feasibility, New Technology and Prototyping Development, Teva Pharmaceuticals
Mark DeStefano

Mr. Mark DeStefano is Director, Combination Products and Devices Research and Development for Teva Pharmaceuticals focusing on advanced technology identification and development for Teva pipeline products. He is an experienced Device Development Professional with a demonstrated 30yr history of product innovation, design, development, and launch in many areas of the medical device industry. Mr. DeStefano holds a Bachelor of Science in Mechanical Engineering from Drexel University.

Mark Tunkel

Global Category Director Services, Nemera
Mark Tunkel

Mark Tunkel is Director of Business Development for Insight Innovation Center Chicago at Nemera. With more than 20 years of global business development experience and a deep understanding of the marketplace challenges and trends impacting the pharmaceutical industry, Mr Tunkel has advised many of the world’s leading companies on their product development and innovation strategies with an emphasis on driving realisation and the most favourable business outcomes.

Miles Buroker

Human Factors Engineer, UserWise, Inc.
Miles Buroker

Education: BS Biomedical Engineering (Biochemical Emphasis)
Experience: Miles first joined UserWise as an intern for the summer of 2018 and came on as a full-time consultant in mid-2019. He is experienced in
•forming use-related risk analyses and test protocols;
•observing usability study sessions for formative and validation testing;
•preparing test reports, risk-benefit analyses and Human Factors Engineering Submission Reports for FDA;
•providing human factors trainings and workshops;
•and with establishing compliance documentation for IEC 62366:2007, IEC 62366-1:2015, and FDA Guidance Documents.
His focus is predominantly on combination products. Miles brings a wide range of pertinent experience from his undergraduate career, including serving as a research assistant, developing a stress-sensing wearable device and accompanying application, and participation in design studios.
 

Natalie Abts

Head of Human Factors Engineering, Genentech
Natalie Abts

Natalie Abts is the Head of Human Factors Engineering at Genentech, where she manages the team that conducts all human factors activities for Genentech’s drug delivery devices. Prior to joining Genentech, Natalie worked in medical device consulting for seven years with the National Center for Human Factors in Healthcare. Natalie has specialized experience in planning and executing both formative stage usability evaluations and validation studies for medical devices and combination products on the FDA approval pathway. Natalie holds a master’s degree in industrial engineering with a focus on human factors and ergonomics from the University of Wisconsin, where she was mentored by Dr. Ben-Tzion Karsh.

Patricia Hojnoski

Associate Director, Janssen (Johnson & Johnson)
Patricia Hojnoski

Patricia Hojnoski is an Associate Director in Janssen’s Global CMC Regulatory Affairs department. She has over twenty years of Regulatory experience working in devices, drugs, diagnostics, and combination products. She is currently responsible for developing global regulatory strategies related to Janssen combination products and giving guidance to combination product development teams on regulatory requirements. She is a member of the Marketing Submissions Combination Products Coalition (CPC) working group.
Patricia has a Bachelor of Science degree in Biology from University of Scranton and a Master of Science degree in Microbiology from Seton Hall University. Additionally, Patricia holds the Regulatory Affairs Certification (RAC-US).
 

Sarah Mollo

Combination Product Policy Analyst, Food and Drug Administration
Sarah Mollo

Sarah Mollo serves as a Combination Product Policy Analyst and Product Jurisdiction Officer in CDRH. Prior to joining the CDRH combination product policy team, Sarah was a lead reviewer and biocompatibility consultant for general hospital devices branch for 3 years before serving the team lead for injection products within OHT3/OPEQ/CDRH. Sarah earned her bachelor’s in Microbiology and Cell Science from the University of Florida and her doctorate in Immunology from the University of Alabama at Birmingham. Prior to joining the FDA she was a post-doc at Harvard University.

Severine Duband

Category Director, Devices, Nemera
Severine Duband

Séverine Duband is Marketing Director for drug delivery Devices at Nemera, steering overall category strategy, product portfolio and innovation development for five key delivery routes. She has been leading the parenteral segment at Nemera since 2018, focusing on proprietary products such as safety systems, pen injectors and on-body injectors. Ms Duband graduated from Emlyon Business School (Lyon, France) in 2004, and joined Nemera’s Global Marketing team in 2018 as a Global Category Manager, focusing on the parenteral segment.

Shannon Clark

CEO, UserWise, Inc.
Shannon Clark

Shannon E. Clark is founder and CEO of UserWise, a consultancy that helps medical device manufacturers and start-ups to design safe and easy-to-use medical devices. The consultants at UserWise conduct usability testing for a variety of medical devices ranging from surgical robots to home-use injection platforms. UserWise consultants also perform safety assessments to comply with U.S. and international regulations related to Human Factors.

Before founding UserWise in 2015, Shannon was a Human Factors Engineer at Intuitive Surgical and Abbott Laboratories.

Shannon graduated from UCLA with a B.S. in Mechanical Engineering and a technical breadth in Technology Management. Shannon is additionally a Certified Processional Industrial Engineer, holds two patents, and has written and published three books.
 

Takuya Minezaki

Research Manager, Mitsubishi Gas Chemical Company, Inc.
Takuya Minezaki

Mr. Minezaki joined Mitsubishi Gas Chemical in 2005. He specializes in the field of synthesis and injection molding of polymer, and has worked in the development of oxygen absorbing polymers. Since 2017, he has worked in the project of new pharmaceutical containers by utilizing oxygen absorbing resins. Also he is in charge of the development of secondary materials, such as plunger stopper and top cap. He holds a Master of Engineering in Applied Chemistry from the University of Tokyo.

Tina Rees

Associate Director, Regeneron Pharmaceuticals
Tina Rees

Tina Rees is the Associate Director of Human Factors at Regeneron Pharmaceuticals. Prior to this, Tina was Associate Director of Human Factors at Ferring Pharmaceuticals, where she was responsible for the development and implementation of Human Factors and Usability Engineering processes into the overall product development process. Here, she worked within the Product Discovery and User Insights group, where they focus on ensuring patient and user centered design occurs throughout the development process. Prior to her move to Ferring, she was a Principal Research Scientist in Human Factors at Eli Lilly, focusing on human factors usability within the diabetes division. She has conducted many formative and summative usability studies and has participated in a number of submissions to regulatory authorities resulting in clearance of medical devices and approval of combination products. She received her Ph.D. in Biomedical Research from the Mayo Clinic in Rochester, MN.

Tracy Hsu

Senior Director, CMC Program Management, Alexion Pharmaceuticals, Inc
Tracy Hsu

Tracy Hsu is Senior Director, CMC Program Management at Alexion Pharmaceuticals. Prior to this, she was Associate Director in the Pharmaceutical Development group at Ionis Pharmaceuticals where she led the drug product and device development aspect for combination products from early stage through commercialization. Prior to Ionis, Tracy led the Biologics Combination Product Development group at Gilead Sciences and served as the Drug Product Technical lead for late stage combination product programs at Amgen. Her experience includes the development of oligonucleotide and biologic drug products in prefilled syringes and autoinjectors.

sponsors

Conference agenda

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8:00

Chairs' Opening Remarks

Natalie Abts, Head of Human Factors Engineering, Genentech

Tina Rees, Associate Director, Regeneron Pharmaceuticals

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8:10

Human factors – best practices

Tina Rees, Associate Director, Regeneron Pharmaceuticals

  • Human factors regulatory requirements
  • Timing of Human Factors studies during development
  • Attributes for good pre-filled syringe design considering common syringe tasks
  • Key considerations for future best practices
     
  • clock

    8:40

    Scope and Method Selection for Human Factors Assessments

    Natalie Abts, Head of Human Factors Engineering, Genentech

  • Different types of human factors assessments that can be used during development
  • Choosing the right assessment method for project needs
  • Factors in appropriately scaling human factors efforts
  • Adapting strategy to accommodate timeline and cost constraints

     

  • clock

    9:10

    Leveraging the patient journey to optimize device use in home care environment

    Severine Duband, Category Director, Devices, Nemera

  • A changing landscape for parenteral administration
  • Understanding the patient journey to provide better outcomes
  • A new generation of passive, add-on safety devices for larger volume biologic drugs
  • How can integrated services support the development of safe, effective, and differentiated combination products
  • clock

    9:50

    Morning Break and Virtual Exhibitor Hall Open

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    10:20

    Selection and development considerations for on-body injectors

    Aly McDonald, Human Factors Engineer, Genentech

    • On-body injector features to evaluate during device selection
    • Usability study considerations and insights
    • Common usability challenges for on-body injectors and guidance in overcoming these
     

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    10:50

    Regulatory Expectations for Real-Life Patient Handling Studies

    Patricia Hojnoski, Associate Director, Janssen (Johnson & Johnson)

  • When are Real Life Patient Handling (RLPH) studies expected?
  • Aligning with FDA on meeting RLPH expectations
  • Leveraging RLPH data between different products
  • Examples of recent FDA RLPH feedback
  • clock

    11:20

    Networking Break and Virtual Exhibitor Hall Open

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    12:20

    Regulatory Considerations for Combination Products

    Sarah Mollo, Combination Product Policy Analyst, Food and Drug Administration

  • Overview of combination products
  • Update on current FDA guidance for combination products
  • Review considerations for combination products
  • Recommendations for engagement with the Agency
  • clock

    12:50

    FDA training decay research initiative – an update

  • An overview of the pilot study
  • A review and assessment of the findings
  • How the findings can be applied in practice
     
  • Shannon Clark, CEO, UserWise, Inc.

    Miles Buroker, Human Factors Engineer, UserWise, Inc.

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    13:20

    Afternoon Break and Virtual Exhibitor Hall Open

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    13:50

    Post-Market safety reporting (PMSR) for combination products - FDA perspective and the global impact

    Khaudeja Bano, Executive Medical Director, Combination Product Safety Head, Amgen

  • FDA has pushed out their post-market reporting for the second year in a row – how has it changed and what does industry need to be aware of? 
  • How does FDA review and regulate combination products? 
  • How can industry adapt to the global divergence of reporting in the marketplace? 
  • Considerations for PMSR compliance and drug/device application
  • We are now close to implementation – what are some of the immediate things you can do as a preparation check?
     
  • clock

    14:20

    Latest data on OXYCAPT Multilayer Plastic Vial & Syringe

    Takuya Minezaki, Research Manager, Mitsubishi Gas Chemical Company, Inc.

  • New Extractables Study
  • Oxygen and Ultraviolet Barrier 
  • Container Closure Integrity by Dye and Helium
  • Staked Needle Syringe
     
  • clock

    15:00

    Chairs' Closing Remarks and Close of Day One

    Natalie Abts, Head of Human Factors Engineering, Genentech

    Tina Rees, Associate Director, Regeneron Pharmaceuticals

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    8:00

    Chairs' Opening Remarks

    Natalie Abts, Head of Human Factors Engineering, Genentech

    Tina Rees, Associate Director, Regeneron Pharmaceuticals

    clock

    8:10

    Designing a Smart Pre-Filled Syringe Platform to Create Value for Patients and Industry

    Jace Blackburn, Smart Device Engineer, Genentech

  • Establishing an internal market research plan to understand the value of Smart Devices for your organization 
  • Structuring and executing an external market research program to understand value to users
  • Following a defined process for selecting platform features
  • What to consider when creating a platform to serve multiple different digital strategies for the business
     
  • clock

    8:40

    The promise and challenges of connected drug delivery devices

    Amin Sedighiamiri, Engineering Manager, Device Development, AstraZeneca

    • Potential value of connected drug delivery devices and barriers to their adoption.
    • Challenges and considerations of designing and developing connected devices

    clock

    9:10

    Morning Break and Virtual Exhibitor Hall Open

    clock

    9:40

    Leveraging Platforms for Combination Product Development

    Tracy Hsu, Senior Director, CMC Program Management, Alexion Pharmaceuticals, Inc

  • Devices suitable for platform approach
  • Design control documentation efficiencies
  • Clinical and Human Factors considerations and case studies
     
  • clock

    10:10

    Panel Discussion: Platform approaches for combination products and pre-filled syringes

  • When is it appropriate to develop a platform for a device?
  • Design and development considerations
  • Preparing the technical development of the platform
  • Selecting a design and development partner for platform devices
     
  • Jace Blackburn, Smart Device Engineer, Genentech

    Tracy Hsu, Senior Director, CMC Program Management, Alexion Pharmaceuticals, Inc

    Mark DeStefano, Director CPD – Feasibility, New Technology and Prototyping Development, Teva Pharmaceuticals

    James Wabby, Executive Director, Head of Regulatory Strategy, Emerging Technologies and Combination Products, AbbVie

    clock

    10:50

    Networking Break and Virtual Exhibitor Hall Open

    clock

    11:50

    Technical Overview of COP for Prefilled Syringes

    Larry Atupem, Sr Business Development Specialist, Zeon Specialty Materials

  • Key properties of COP
  • Case Study (New): 
  • Protein Adsorption of Abatacept – COP vs Glass
  • Immunogenicity test of the aggregates
  • Case Study: Protein Adsorption of Humira, Embrel, Remicade – COP vs Glass
  • Case Study: Protein Adsorption with/without Polysorbate (Surfactant) – COP vs Glass
  • Leachable data on COP syringes
     
  • clock

    12:30

    PATH’s Initiatives in Developing Next Generation Injectables – The Journey from Needle Free to Micro-Array Patches

    Darin Zehrung, Global Program Leader , PATH

  • PATH’s overview of work on injectable device and vaccine innovations, and Center of Excellence for Microarray Patch (microneedle) technology
  • Value proposition and cost modelling of alternatives to traditional PFS
  • Clinical data to demonstrate efficacy of novel vaccine delivery devices
  • Engineering challenges and opportunities ahead
     
  • clock

    13:00

    Afternoon Tea

    clock

    13:30

    Usability considerations for large-volume injectors

    Mark DeStefano, Director CPD – Feasibility, New Technology and Prototyping Development, Teva Pharmaceuticals

  • Target users vs right technology 
  • How easy can you make it, simpler is better but users need to know what is happening.
  • Familiarity, Leveraging what user already know or have seen.
  • Dosing Frequency Considerations vs technology complexity. What does the user remember
     
  • clock

    14:00

    How Safe Are My Devices? Regulatory Compliance Lifecycle Management of Combination Products

    James Wabby, Executive Director, Head of Regulatory Strategy, Emerging Technologies and Combination Products, AbbVie

  • Understanding User Needs and Usability
  • Quality System Requirements
  • Design Control and Product Development Management
  • Case Studies on Clinical Trials and Complaint Management
     
  • clock

    14:30

    Chairs' Closing Remarks and Close of Day Two

    Natalie Abts, Head of Human Factors Engineering, Genentech

    Tina Rees

    Tina Rees, Associate Director, Regeneron Pharmaceuticals


    Human Factors Engineer
    Genentech
    Engineering Manager, Device Development
    AstraZeneca
    Global Program Leader
    PATH
    Smart Device Engineer
    Genentech
    Executive Director, Head of Regulatory Strategy, Emerging Technologies and Combination Products
    AbbVie
    Executive Medical Director, Combination Product Safety Head
    Amgen
    Sr Business Development Specialist
    Zeon Specialty Materials
    Director CPD – Feasibility, New Technology and Prototyping Development
    Teva Pharmaceuticals
    Global Category Director Services
    Nemera
    Human Factors Engineer
    UserWise, Inc.
    Head of Human Factors Engineering
    Genentech
    Associate Director
    Janssen (Johnson & Johnson)
    Combination Product Policy Analyst
    Food and Drug Administration
    Category Director, Devices
    Nemera
    CEO
    UserWise, Inc.
    Research Manager
    Mitsubishi Gas Chemical Company, Inc.
    Associate Director
    Regeneron Pharmaceuticals
    Senior Director, CMC Program Management
    Alexion Pharmaceuticals, Inc

    Sponsors

    Exhibitors

    Official Media Partner

    Supporting Media Partners

    Preliminary Attendees List 2021

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    Speaker Interview with Aly McDonald, Grenentech

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    Speaker interview with Natalie Abts, Genentech

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    Speaker interview with Jace Blackburn, Genentech

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    Speaker interview with Mark Destefano, Teva Pharmaceuticals

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    Speaker interview James Wabby, Allergan

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    Past Attendee List

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    Infographic 2021

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    Speaker Bios

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    2 Day Programme Short

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    2 Day Programme Long

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    Brochure 2021

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    Past Presentation Shannon Clark UserWise.Inc

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    Past Presentation Walter Goodwin Gilead Sciences

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    Past Presentation Jonathon Sutch BSi

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    Past Presentation Christine Lynn Merck & Co.Inc

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    Past Presentation Mark Hassett Credence Medsystems

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    Past Presentation Juha Matilla Steris

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    Past Presentation Larry Atupem Zeon

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    Past Presentation Jace Blackburn Genentech

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    Past Presentation Hiroki Hasegawa Mitsubishi Gas Chemical

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    Past Presentation James Leamon Jazz Pharmaceticals

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    POST CONFERENCE REPORT

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    Chair Letter 2021

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    Sponsors


    Mitsubishi Gas Chemical

    Sponsors
    https://www.mgc.co.jp/eng/products/abd/oxycapt.html

    Mitsubishi Gas Chemical is a leading company in the field of oxygen barrier and absorbing technologies. Based on these technologies and experiences, we have successfully developed multilayer plastic vial and syringe having excellent oxygen, ultra violet and water vapor barrier. The products make it possible to replace glass with plastic for injectable drugs.


    Nemera

    Sponsors
    http://www.nemera.net

    As a world-leading drug device combination solutions specialist, our purpose of putting patients first enables us to design and manufacture devices that maximize treatment efficacy. We are the utmost holistic partner and help our customers succeed in the sprint to market. From early device strategy to state-of-the-art manufacturing, we’re committed to the highest quality standards. Agile and open-minded, we work with our customers as colleagues. Together, we go the extra mile to fulfill our mission. Nemera leverages decades of experience in the parenteral device segment from full development to pure contract manufacturing, through customized solutions. Nemera developed - Safe’n’Sound®, a fully passive safety device for prefilled syringes to avoid accidental needle-sticks and - Wearables, technological bricks combined together into a smart wearable to improve patients’ life.


    ZEON

    Sponsors
    http://www.zeonex.com

    ZEON’s Zeonex® and Zeonor® cyclo olefin polymer (COP) allow for advanced, break-resistant syringes, vials and lyophilization containers for protein-based biopharmaceuticals, high viscosity drugs, and contrast media. They also offer high purity, “glass-like” transparency, sterilization, low water absorption, and superior moldability, as well as overcome protein adsorption and ph shift concerns.

    Exhibitors


    Heuft

    Exhibitors
    https://pharma.heuft.com/en

    Quality, safety and efficiency: this is what matters when filling and packaging pharmaceuticals! The modular solutions from HEUFT SYSTEMTECHNIK GMBH put these key factors into practice simply and effectively. They ensure, during maximum productivity, that only perfect pharmaceutical products reach the market! The Heuft Syringer ensures the safeguarding of the integrity, quality and functionality of pre-filled syringes right from the start. The HEUFT Syringer can be integrated into the assembly process easily for this purpose. It detects safety, functional and quality defects on pre-filled syringes during the assembly process with smart optics and a unique pulsed X-ray inspection to peer below the needle shield!



    Novo Engineering

    Exhibitors
    http://www.novoengineering.com

    NOVO provides contract product development services to medical device and life science customers, helping them to bring better devices to market. Faster. Our team of 55 hardware and software developers has delivered hundreds of commercialized products and are inventors on more than 400 patents.

    NOVO’s systems engineering expertise makes us well-suited to the development of complex devices that communicate to cloud servers directly or via mobile device hosts.

    Medical device experience includes endoscopy – drug delivery – continuous glucose monitoring – transcatheter delivery systems – intragastric implants – infusion devices – on-body injectors – cardiac monitoring – closed-loop insulin delivery – and connected devices.

    For our customer’s convenience, both our California and Minnesota locations offer onsite rapid prototyping, CNC machining and product testing facilities. Advanced facilities combined with an ISO 13485-certified quality system tailored to product development, create the ideal environment for the innovations that our customers demand. Visit us at www.novoengineering.com.



    Owen Mumford

    Exhibitors
    http://www.ompharmaservices.com

    Owen Mumford Pharmaceutical Services is a specialist in the design, development and manufacture of injectable drug delivery systems for the pharmaceutical, biotech & generics industries. These include single dose and multidose reusable and disposable auto-injectors, pens and syringes for subcutaneous and intramuscular administration. Our innovative products are designed to meet both the need of our pharmaceutical partners and their patients by facilitating ease of use and improving safety and patient compliance. Our devices are also designed with aim of reducing complexity and risk for the pharmaceutical & biotech industry in the development of their combination products.

    Media Partners


    Medical Design Briefs

    Official Media Partner
    http://WWW.TECHBRIEFS.COM/SUBSCRIBE/MDB/SMIEAST21

    Medical Design Briefs (MDB) is the only publication for the medical OEM market dedicated to medical product design engineers and managers. We offer timely, accurate, quality content and editorial, and we report on engineering-related topics that are at the core of the latest medical technologies. From materials to manufacturing, we dive into the technical side of bringing medical devices to market. From biosensors to cybersecurity, we keep our fingers on the pulse of the hottest trends and topics that may augment or disrupt medical technology.


    ONdrugDelivery Magazine

    Official Media Partner
    http://ondrugdelivery.com

    ONdrugDelivery provides 30,000 readers throughout global pharma/biopharma, with the latest, most pertinent industry information and intelligence about the drug delivery-related ideas, technologies, services and products the sector is developing. Established in 2004, and trusted throughout the industry for its high quality contributions from leading drug delivery experts, ONdrugDelivery is a must for pharma / biotech industry professionals who need to know what’s going on in drug delivery. Subscribe online today to the print or free digital edition: www.ondrugdelivery.com/subscribe.


    American Pharmaceutical Review

    Official Media Partner
    http://www.americanpharmaceuticalreview.com

    Start receiving your free copy today. American Pharmaceutical Review is a review of the drug pipeline from the late discovery phase through manufacturing. American Pharmaceutical Review prides itself on having the most relevant, unbiased and informative editorial in the industry. You will find that all of our editorial is highly technical and written by government agencies, consultants, academics, and large pharmaceuticals companies. American Pharmaceutical Review covers several key topics that are important to drug production:Separations and purification, Drug Delivery, Biopharmaceutical Processing, Biopharmaceutical Development, Formulation development, Manufacturing, Microbiology, Instrumentation, Spectroscopy

    Media Partners


    BioPharm Insight

    Supporting Media Partners
    http://www.biopharminsight.com

    BioPharm Insight is your definitive guide to the global life sciences community. Subscribers take action on forward-looking intelligence uncovered by an independent team of investigative journalists, and make strategic business decisions using the most comprehensive and powerful real-time database of market analytics and key contacts. Featuring an intuitive online interface and exclusive Active IntelT relational content technology, BioPharm Insight provides an unrivaled capability to segment and analyze the industry with detailed and searchable profiles.


    Drug Discovery Today

    Supporting Media Partners
    http://www.drugdiscoverytoday.com/

    Drug Discovery Today covers the whole of the preclinical drug discovery process. The reviews are cutting edge, written by experts in their respective fields and cover all aspects of drug discovery from genomic and proteomic approaches, computational drug design, medicinal chemistry and the translation of these sciences to therapies.


    World Pharma News

    Supporting Media Partners
    http://www.worldpharmanews.com/



    Pharmacircle

    Supporting Media Partners
    http://www.pharmacircle.com

    PharmaCircle is an innovative knowledge management company serving the current and future global leaders in the Pharmaceutical and Biotechnology related industries. PharmaCircle is a one stop information and analysis source for pipeline, products, clinical trials, drug delivery technologies, deals and acquisitions, company financials, venture capital investments, product sales, pharmaceutical services, news, patents and more….


    Pharma Journalist

    Supporting Media Partners
    http://www.pharmajournalist.com

    Pharma Journalist is a product of Kellen Media. Pharma Journalist is one of the leading website covering the need of global Pharmaceutical Industry. Articles like latest news, trends, analysis, market report, press releases, whitepapers, case studies, etc. published on pharmajournalist.com helps Industry professionals and decision makers to stay on the top of this fast-paced industry. Pharma Journalist aims of providing fast and informative articles to its readers and subscribers.


    PharmaVOICE

    Supporting Media Partners
    http://www.pharmavoice.com

    PharmaVOICE magazine, and its supporting VIEW publications, provide commentary about the challenges and trends impacting the life-sciences industry, covering a range of issues from molecule through market. PharmaVOICE's more than 41,000 U.S.-based subscribers are also kept abreast of the latest trends through additional media resources, including WebSeminars, Podcasts, Videocasts, and White Papers.


    Pharmaceutical Outsourcing

    Supporting Media Partners
    http://www.pharmoutsourcing.com

    Pharmaceutical Outsourcing, the journal dedicated to pharmaceutical and biopharmaceutical contract services. With regular sections on contract manufacturing, contract research, contract packaging, formulation/development services, contract analytical testing, APIs, stability testing, clinical research and other areas, we bring the most complete coverage of trends and issues in the industry to our 15,000 readers in North America.


    Pharmaceutical Technology

    Supporting Media Partners
    http://www.pharmaceutical-technology.com

    Pharmaceutical-technology.com is the only website focusing specifically on issues relevant to pharmaceutical professionals working with technology, be it development, engineering, IT or production. Pharmaceutical-technology.com brings you the latest in industry projects and updates, along with the news, views and trends that leading professionals – from senior executives to manufacturing managers and heads of procurement – require to stay on top of their field.


    pharmaphorum

    Supporting Media Partners
    http://www.pharmaphorum.com

    pharmaphorum drives innovation within the pharmaceutical industry, by bringing healthcare together through a suite of media services that help produce and disseminate thought leadership, combined with an online platform for communicating messages to a global audience.Visit www.pharmaphorum.com


    Pharmalicensing

    Supporting Media Partners
    http://www.pharmalicensing.com

    Pharmalicensing (www.pharmalicensing.com) is the premier biopharmaceutical Open Innovation resource designed for professionals involved with partnering, licensing and business development worldwide. Actively supporting all forms of partnering and in- and out-licensing activities, Pharmalicensing utilizes the unique online Showcase Profiling & Discover services, as well as its renowned Partnering Search service leveraging its global network of industry experts, to enable companies to identify and engage with appropriate partners around the world. Pharmalicensing is actively utilized by many tens of thousands of industry professionals each month. Pharmalicensing is a division of Cognis Group, Inc


    pharmanews hq

    Supporting Media Partners
    http://http://pharmanewshq.com

    MedChemNet provides a unique and unparalleled platform for the medicinal chemistry community to share insights, discuss the latest research, and help move the field forward. MedChemNet covers all aspects of the drug discovery pipeline, from target identification and validation, through computer aided drug design (CADD), synthesis, screening and other biophysical techniques, to development of novel lead compounds and pre-clinical in vivo proof of concept. We also cover the design of synthetic drug delivery carriers and ADME/toxicology studies, as well as intellectual property and economic related issues. Website: Welcome to Pharma News HQ, the journal dedicated to the pharmaceutical and biopharmaceutical contract services. With regular sections on contract manufacturing, contract research, contract packaging, formulation/development services, contract analytical testing, APIs, stability testing, clinical research and other areas, we bring the most complete coverage of trends and issues in the industry. Pharmanewshq.com is the only website focusing specifically on issues relevant to pharmaceutical professionals working with technology, be it development, engineering, IT or production.


    Pharmiweb

    Supporting Media Partners
    http://www.pharmiweb.com

    Established in October 2003, PharmiWeb Solutions is an energetic, innovative provider of web-based solutions for the pharmaceutical sector, with customers such as AstraZeneca, Roche, Servier Laboratories, and Merck With solutions in three key areas: Online Publishing, e-Business and Mobile Computing, we deliver connectivity – between people and applications – unlocking islands of data and knowledge. We own some of the sector’s most innovative Online Publications: PharmiWeb.com, HospitalPharma.com and Detail-Direct.com. We are actively developing solutions for Mobile Computing platforms. For example, our PharmiTabTM e-pharmacy solution runs real-time patient data and prescribing transactions in a busy hospital environment, on a TabletPC, wireless client/server platform. e-Business solutions range from e-Detailing, to Online Market Research, all designed to increase reach, increase sales, and to reduce administration and costs.


    Farmavita

    Supporting Media Partners
    https://farmavitar.com

    FarmavitaR+ is the professional network of experts and service providers. Network is gathering local consultants from 90 countries in Europe, Asia, North America, Latin America, Australia and Africa. Management of international, multi-centre projects is our core competence. FarmavitaR+ is providing solutions related to pharmaceutical, medical device, food supplement and cosmetic products. Scope of services is related to solutions for product development, quality assurance, clinical trials, product registration, portfolio analysis, lifecycle management, vigilance/risk management, pricing/reimbursing, market access and promotional compliance. FarmavitaR+ is brand name of Farmavita Regulanet Ltd. Visit https://farmavitar.com for more information. Outsource anything you can think of!


    Biocompare

    Supporting Media Partners
    http://www.biocompare.com

    Biocompare.com is the leading resource for up-to-date product information, product reviews, and new technologies for life scientists. Biocompare combines an in-depth knowledge of life science products and new technologies with the power of the Internet to offer scientists the most dynamic, relevant, and innovative media-based marketplace for life science information.


    Technology Networks

    Supporting Media Partners
    http://go.technologynetworks.com/subscribe-to-newsletters

    Founded in 2000, Technology Networks is established as the leading news provider for life science and drug discovery professionals. In addition, we provide unique content including webcasts, videos, application notes and posters from recent conferences. Our portfolio now includes around 30 focussed scientific communities, all of which are accessible free of charge within TechnologyNetworks.com


    IPI

    Supporting Media Partners
    http://www.ipimediaworld.com

    IPI – International Pharmaceutical Industry Established by professionals with over 30 years experience in the Pharmaceutical and Life sciences publishing sectors. We have identified the needs of these dynamic industries, and have listened carefully to our readers and advertisers. With strong collaboration between Pharmaceutical and Life sciences Industry Associations we have created a global distribution network. We give you a promise to become a reliable extension of your marketing and communication arm. If necessary we will integrate our expertise with your needs. Incorporating new and innovative communication methods we will help to highlight your expertise.


    Pharmavision

    Supporting Media Partners
    http://www.pharmavision.co.uk

    PharmaVision offers a consultancy service providing independent pharmaceutical thematic research to the healthcare industry, the investment community and competitive intelligence specialists. We perform due diligence research and provide expert commentary in healthcare. Our reports combine scientific analysis in drug delivery, R&D technologies and pharmaceutical products including patient modelling, product/technology forecasts and market trends evaluation.


    Gate2Biotech

    Supporting Media Partners
    http://www.gate2biotech.com

    Gate2Biotech is a portal that unites biotechnological community in Central Europe. It covers all the news in the field of biotechnology. Thanks to the the portal the companies engaged in the field can easily search for research institutions and other partners to solve technical problems they are facing and here they can also present their services offer to potential partners from the Czech Republic and abroad. Gate2Biotech portal serves as a bridge connecting scientific and commercial sector. It incorporates offices and support organizations dedicated to promoting transfer of innovative technologies into a unified communication platform of Czech and international biotechnologies. As a mediator of information it draws attention to biotechnologies and support of their application and transfer into practice. It also functions as a tool for encouraging non-professionals (especially scientists and students) towards innovative business or applied research.

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    WHAT IS CPD?

    CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

    ‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

    CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

    Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

    CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

    CPD AND PROFESSIONAL INSTITUTES

    There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

    For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

    CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

    TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

    Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

    ‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

    ‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

    The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

    As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

    GLOBAL CPD

    Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

    CPD Certificates

    We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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    Contact SAE Media Group

    UK Office
    Opening Hours: 9.00 - 17.30 (local time)
    SAE Media Group , Ground Floor, India House, 45 Curlew Street, London, SE1 2ND, United Kingdom
    Tel: +44 (0) 20 7827 6000 Fax: +44 (0) 20 7827 6001
    Website: http://www.smgconferences.com Email: events@saemediagroup.com
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