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Pre-Filled Syringes West Coast

CONFERENCE: JUNE 5TH & 6TH 2017
INTERACTIVE WORKSHOP: JUNE 7 2017 (VISIT THE "ASSOCIATED EVENTS" TAB FOR DETAILS)

SAE Media Group are thrilled to announce the return of Pre-Filled Syringes West Coast 2017 which arrives to California on June 5th & 6th.

Following on from sell-out shows in Europe and Boston, Pre-Filled Syringes West Coast will once again gather a global audience of medical device experts and PFS industry leaders to discuss new developments and showcase cutting edge advancements, keeping you at the forefront of a booming industry.

The competitive PFS market has sparked great improvements as devices strive for higher quality, safety, and patient satisfaction. Innovation and excellence is requested at every level making Pre-Filled Syringes West Coast the perfect platform to strengthen knowledge in key principles such as human factor engineering, manufacturing and complex biologics, whilst honing in on emerging trends for parenteral devices, including auto injectors, pens, pumps and smart devices.

Hear from a selection of carefully handpicked keynote addresses and case studies presented by big pharma such as Genentech, Allergan, Medimmune and Roche as well leading industry KOL's including Nemera, Nipro PharmaPackaging, Terumo, Worrell, Zeon + more!

“It is critical to develop working relationships and collaborations, as an industry, to bring knowledge to the suppliers and drug developers worldwide, so that we can address these challenges. Thank you to everyone who contributes to this goal and looking forward to your participation at the conference." - Speaker and Conference Chair: Mike Stelmah, Senior Manager, Combination Products Regulatory Affairs, Regeneron


 

FEATURED SPEAKERS

John  Smith

John Smith

Director, Global Regulatory Affairs , Allergan
Matt Gottschalk

Matt Gottschalk

Medical Device Consultant , Worrell
Mayumi Bowen

Mayumi Bowen

Senior Engineer, Genentech, Inc.
Tina Rees

Tina Rees

Associate Director - Human Factors , Ferring

Aaron Chesterman

Device Development Engineer, Genentech
Aaron Chesterman

Adrien Tisserand

Category Manager - Parenteral, Nemera
Adrien Tisserand

Alasdair Young

Device Engineer, Genentech / Roche
Alasdair Young

Anand Subramony

Vice President Drug Delivery & Device Development, MedImmune
Anand Subramony

Ann Peirce

Area Sales Manager, Nipro PharmaPackaging
Ann Peirce

Ariel Waitz

Senior Engineer, Genentech
Ariel  Waitz

Benir Ruano

Vice President, Global Manufacturing & Technical Operations, Xeris Pharmaceuticals
Benir Ruano

John Smith

Director, Global Regulatory Affairs , Allergan
John  Smith

Lori de los Reyes

Director, Global Regulatory Affairs, Amgen
Lori de los Reyes

Matt Gottschalk

Medical Device Consultant , Worrell
Matt Gottschalk

Mayumi Bowen

Senior Engineer, Genentech, Inc.
Mayumi Bowen

Mike Stelmah

Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals
Mike Stelmah

Monica De Bardi

Post Doctoral Researcher , F. Hoffmann-La Roche Ltd
Monica De Bardi

Nan Yung Lin

Consultant, Freelance
Nan Yung Lin

Ronald Forster

Director Process Development, Amgen
Ronald Forster

Sara McNew

Human Factors Engineer , Eli Lilly
Sara McNew

Serge Dubeau

Vice President of Design and Human Factors , Worrell
Serge Dubeau

In his nearly 20 years of experience, Serge has led design and engineering teams in a variety of projects for both Fortune 100 and start up companies, resulting in various design awards and more than a dozen patents. He currently leads the design and human factors engineering teams at Worrell, focusing on user and patient safety. He holds a degree in Industrial Design from the University of Montreal, and is multi-lingual, having lived and worked in Spain, Canada and the United States.

Shota Arakawa

Researcher , Mitsubishi Gas Chemical America Inc
Shota Arakawa

Tina Rees

Associate Director - Human Factors , Ferring
Tina Rees

Toshiro Katayama

Product Manager, Zeon Chemicals L.P.
Toshiro Katayama

William Dierick

Director Technology Development, Terumo Europe
William Dierick

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Workshop Leader's opening remarks and introduction

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9:10

Incorporating Human Factors into prefilled device development

Melanie Turieo

Melanie Turieo, Director, Human Factors Engineering, Cambridge Consultants Ltd

• What to consider when making your device Human
o Design Intent
o Tests and evaluations
o Seeking regulatory approval – what to provide to gain regulatory approval

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9:40

Case study examples – common pitfalls vs success stories

Melanie Turieo

Melanie Turieo, Director, Human Factors Engineering, Cambridge Consultants Ltd

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10:10

Discussion

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11:00

The bigger picture; Human Factors as an ecosystem consideration

Melanie Turieo

Melanie Turieo, Director, Human Factors Engineering, Cambridge Consultants Ltd

• Human Factors is not a stand-alone consideration
• Balancing safety, usability and commercial success

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12:00

Discussion

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12:30

Workshop leader’s comments and close of workshop

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

Mike Stelmah

Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals

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9:10

Navigating the global regulatory ecosystem

John  Smith

John Smith, Director, Global Regulatory Affairs , Allergan

• Taking into account regulatory requirements for USA, Europe and ROW to ensure your product’s success on a global market
• Update on key points from different regulatory bodies
• What to consider when seeking approval; safety assessments, Human factors considerations

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9:45

Navigating technical complaints, product safety and regulatory requirements

Mike Stelmah

Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals

• Taking into account regulatory requirements for product safety and complaint handling
• Update on key product failures and challenges
• What to consider while planning safety assessments, risk analysis and complaint handling for clinical studies and commercial

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10:20

Morning Coffee sponsored by Terumo

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10:50

Large volume subcutaneous infusion devices; in vivo and in vitro challenges

• Drivers for large volume SC delivery
• Technical criteria when evaluating devices for large volume SC delivery
• Use of large volume SC devices in clinic, including potential complicating factors

Ariel  Waitz

Ariel Waitz, Senior Engineer, Genentech

Aaron Chesterman

Aaron Chesterman, Device Development Engineer, Genentech

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11:25

PLAJEX with safe ‘n’ sound; safe delivery of biotherapeutics

• Polymer PFS are developed for providing an appropriate primary drug container, particularly for biopharmaceuticals.
• A platform of add-on passive sharps injury protection devices for PFS are serving the patients and healthcare providers for minimizing the risks of needle-stick injuries.
• A cooperation to establish and confirm compatibility between PLAJEX COP prefillable syringes and the Safe’n’Sound device platform

Adrien Tisserand

Adrien Tisserand, Category Manager - Parenteral, Nemera

William Dierick

William Dierick, Director Technology Development, Terumo Europe

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12:05

Networking lunch sponsored by Worrell

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13:15

Combination product data bridging

Lori de los Reyes

Lori de los Reyes, Director, Global Regulatory Affairs, Amgen

•  Guidance on clinical bridging, examples of when clinical bridging may be necessary
• Clinical home use study design
• Examples of FDA feedback on the need for clinical home use
• Leveraging pre-existing data and Human factors

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13:50

Combination products, a need for innovative and customizable drug delivery devices

Adrien Tisserand

Adrien Tisserand, Category Manager - Parenteral, Nemera

  • Parenteral market trends
  • Drug, device, users considerations
  • Device design challenges
  • Case study: Safelia® autoinjector
  •  

     

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    14:30

    Afternoon Tea sponsored by Terumo

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    15:00

    OXYCAPT™ multilayer plastic vial & syringe with glass-like gas barrier for biologics

    Shota Arakawa

    Shota Arakawa, Researcher , Mitsubishi Gas Chemical America Inc

    • Glass vs. plastic
    • Disadvantages of plastic
    • How to overcome the disadvantages of plastic

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    15:40

    An approach to developing risk-based control strategies for combination products

    Alasdair Young

    Alasdair Young, Device Engineer, Genentech / Roche

    • Defining and establishing critical quality attributes for a combination product
    • Utilizing a risk-based approach to defining a control system
    • A case study on deployment of the control strategy process for a combination product

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    16:15

    Glucagon synthetic peptide formulation in PFS filled auto-injector combination product platform

    Benir Ruano

    Benir Ruano, Vice President, Global Manufacturing & Technical Operations, Xeris Pharmaceuticals

    • Challenges with a non-aqueous drug formulation compatibility with PFS components
    • Challenges with manufacturing aseptically filled low fill volume PFS
    • Challenges with an international supply chain

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    16:50

    Panel Discussion: The future of parenteral drug delivery

    • On the road to patient-centric drug delivery - understanding the patient's interaction with the delivery system to be able to incorporate features which promote adherence to treatments
    • Identifying the good manufacturing regulations that apply to combination products
    • Technical challenges for developing and manufacturing combination products
    • Regulatory hurdles in obtaining approval for pre-filled syringes and pens in human factors studies

    John  Smith

    John Smith, Director, Global Regulatory Affairs , Allergan

    Anand Subramony

    Anand Subramony, Vice President Drug Delivery & Device Development, MedImmune

    Tina Rees

    Tina Rees, Associate Director - Human Factors , Ferring

    Sara McNew

    Sara McNew, Human Factors Engineer , Eli Lilly

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    17:25

    Chairman’s Closing Remarks and Close of Day One

    Mike Stelmah

    Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals

    clock

    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Mike Stelmah

    Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals

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    9:10

    Creating patient centric combination products

    Anand Subramony

    Anand Subramony, Vice President Drug Delivery & Device Development, MedImmune

    • Patient centricity
    • Connected health
    • Drug delivery

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    9:50

    How mixed reality will drive the future of drug delivery product development

    • What does virtual reality mean for ethnography and human factors testing?
    • How can we use augmented reality to impact device development & sales?
    • How can we apply this to the frontlines of healthcare?

    Matt Gottschalk

    Matt Gottschalk, Medical Device Consultant , Worrell

    Serge Dubeau, Vice President of Design and Human Factors , Worrell

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    10:30

    Morning Coffee sponsored by Terumo

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    11:00

    Giving the device a Human touch

    Sara McNew

    Sara McNew, Human Factors Engineer , Eli Lilly

    • The role of patient centricity in drug delivery and device development
    • Successfully incorporating Human factors into device design
    • Human factors regulations and guidelines for successful approval

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    11:40

    Human Factors implications of innovative delivery systems for biologics

    Tina Rees

    Tina Rees, Associate Director - Human Factors , Ferring

    • Overview of alternatives to prefilled syringes in parenteral drug delivery, such as autoinjectors, patches, pumps, and pens
    • Performing formative and summative human factors studies with alternative delivery systems
    • Examples of development and human factors validation of innovative delivery systems

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    12:20

    Networking Lunch

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    13:30

    Driving particles to zero

    Ronald Forster

    Ronald Forster, Director Process Development, Amgen

    • Intrinsic particles: What are the specific challenges presented by the silicone layer, and silicone oil free systems
    • Extrinsic particles: supplier to fill finish
    • Considerations for combination products
    • Case study examples of silicone free devices; what are the pros and cons?

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    14:10

    COP- Technical data update

    Toshiro Katayama

    Toshiro Katayama, Product Manager, Zeon Chemicals L.P.

    • Key properties of COP – demonstrating the value and characteristics of COP compared with glass
    • Case study: Study on protein adsorption/aggregation with actual protein drug – COP vs. glass
    • Case study: Study on delamination with glass syringe vs. COP syringe
    • Leachable data on COP syringe with various chemicals

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    14:50

    Sterilization Development and Validation for Biological Drug Device Combination Products

    Mayumi Bowen

    Mayumi Bowen, Senior Engineer, Genentech, Inc.

  • Challenges for external surface sterilization of syringes filled with biologics
  • Strategies and points to consider for sterilization development
  • Case studies and lessons learned from experience
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    15:30

    Afternoon Tea sponsored by Terumo

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    16:00

    Innovative Technologies in the manufacturing process of glass pre-filled syringes

    Ann Peirce

    Ann Peirce, Area Sales Manager, Nipro PharmaPackaging

    • Introduction of a laser-assisted glass cutting technology resulting in reduced glass particle count, mechanically stronger and more dimensionally stable finger flanges
    • Features and benefits of an innovative X-ray inspection unit addressing increasing regulatory requirements for CCI and for drug delivery systems safety

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    16:40

    Needle clogging in SIN-PFS filled with high concentration protein solution

    Monica De Bardi

    Monica De Bardi , Post Doctoral Researcher , F. Hoffmann-La Roche Ltd

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    17:20

    Panel discussion: The future of parenteral drug delivery

    • Addressing the need and challenges of high volume injectables:
             o Commercial opportunity and challenges
             o User considerations
             o Technologies: Wearable injectors, hand held auto-injectors & syringes etc.
    • Connectivity and connected devices:
             o Are they the future of parenteral drug delivery?

    Mike Stelmah

    Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals

    Nan Yung Lin

    Nan Yung Lin, Consultant, Freelance

    Serge Dubeau, Vice President of Design and Human Factors , Worrell

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    18:00

    Chairman’s Closing Remarks and Close of Day Two

    Mike Stelmah

    Mike Stelmah, Director, Regulatory Affairs CMC & Combination Products, Alnylam Pharmaceuticals


    Device Development Engineer
    Genentech
    Category Manager - Parenteral
    Nemera
    Device Engineer
    Genentech / Roche
    Vice President Drug Delivery & Device Development
    MedImmune
    Area Sales Manager
    Nipro PharmaPackaging
    Senior Engineer
    Genentech
    Vice President, Global Manufacturing & Technical Operations
    Xeris Pharmaceuticals
    Director, Global Regulatory Affairs
    Allergan
    Director, Global Regulatory Affairs
    Amgen
    Medical Device Consultant
    Worrell
    Senior Engineer
    Genentech, Inc.
    Director, Regulatory Affairs CMC & Combination Products
    Alnylam Pharmaceuticals
    Post Doctoral Researcher
    F. Hoffmann-La Roche Ltd
    Consultant
    Freelance
    Director Process Development
    Amgen
    Human Factors Engineer
    Eli Lilly
    Vice President of Design and Human Factors
    Worrell
    Researcher
    Mitsubishi Gas Chemical America Inc
    Associate Director - Human Factors
    Ferring
    Product Manager
    Zeon Chemicals L.P.
    Director Technology Development
    Terumo Europe

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    Pre-Filled Syringes East Coast, Boston

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    TEVA Lisa Nilsson 2016 presentation

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    PFS West Coast 2017 Preliminary List of Attendees

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    2016 PFS West Coast Attendee List

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    Exclusive interview released with Allergan ahead of PFS West Coast 2017

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    MSD Jeffrey Givand 2016 Presentation

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    Sponsors and Exhibitors


    MedicoPack

    Sponsors and Exhibitors
    http://www.medicopack.com

    Manufacturer of medical primary packaging. Plastic vials, bottles (PP, PE, COC, COP, multilayer). Cleanroom facilities Class C/ISO 7. Extensive knowledge on 100% transparent ClearVial. ClearVials is a breakthrough in primary packaging solutions for the pharmaceutical and biotec industries. ClearVials is available in COC (Cyclic Olefin Copolymer) vial or COP (Cyclic Olefin Polymer).


    Mitsubishi Gas Chemical

    Sponsors and Exhibitors
    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.


    Nipro PharmaPackaging

    Sponsors and Exhibitors
    http://www.nipro-group.com

    Nipro PharmaPackaging is specialized in developing and manufacturing advanced pharma packaging products and complete packaging solutions for early development drugs or the enhancement of packaging solutions for existing drugs. With a worldwide manufacturing footprint of 19 plants, multiple sales offices, and lab services, Nipro offers an exceptional service platform. Through our personnel, products, and services, Nipro PharmaPackaging enables you to provide a safer and healthier administration to your customers. Nipro PharmaPackaging is part of Nipro Corporation Japan, established in 1954. As a leading global healthcare company with over 35,000 employees worldwide, Nipro serves the Pharmaceutical, Medical Device, and Pharmaceutical Packaging industries.


    OVLK (Overlook Industries)

    Sponsors and Exhibitors
    http://www.ovlk.com/

    OVLK provides innovative single-use fluid path components for increased liquid filling efficiencies. Ask us about our Freedom Filling Kits, which include all necessary single-use components of the fluid path, multi-bagged and gamma sterilized per customer requirements, as well as our single-use and direct replacement OEM Filling Needles. OVLK will partner with you in determining and offering practical, efficient solutions to your fill/finish manufacturing challenges!


    Sherpa Clinical Packaging

    Sponsors and Exhibitors
    http://www.sherpaclinical.com/?utm_source=conference&utm_medium=partner&utm_campaign=PFS

    Sherpa Clinical Packaging provides clinical trial material management services for clinical studies phases I-IV, including packaging, labeling, distribution, storage and returns and destruction services. Our agile managerial and operational systems are built to accommodate ever-changing clinical project requirements and fast turnaround times without sacrificing quality. Sherpa’s responsive team leverages its global expertise to identify and execute creative clinical supply solutions for all clients.


    Steri-Tek

    Sponsors and Exhibitors
    http://www.steri-tek.com

    Steri-Tek is a high-volume E-beam/X-Ray contract sterilizer and R&D innovation center serving the medical device, biotech, pharmaceutical and other industries. Steri-Tek is a ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as State of California Medical Device and Drug Manufacturing licensed facility. Particularly with sensitive materials and complex devices, Steri-Tek has developed a proprietary system for optimizing E-beam/X-Ray sterilization of drugs/biologics in combination devices, pre-filled syringes, implantables, bioabsorbables and other complex products.


    Terumo Pharmaceutical Solutions

    Sponsors and Exhibitors
    http://www.terumo-ps.com/

    Terumo Pharmaceutical Solutions offers the pharmaceutical and biotechnology industry unique solutions in medical technology. In addition to offering our valued products, our specialized team also provides customized and dedicated solutions designed to meet your specific requirements.


    Worrell

    Sponsors and Exhibitors
    http://www.worrell.com

    Worrell is a multifaceted healthcare design and innovation firm with offices in London, Minneapolis and Shanghai. Worrell provides expertise in research and strategy, user experience and industrial design, human factors engineering and prototyping. Working on the front lines with patients and healthcare professionals, Worrell uncovers unmet needs to bring new drug delivery, medical device, and digital health solutions to the market.


    ZEON

    Sponsors and Exhibitors
    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.

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    Colorado Bioscience

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    As champions for life science in our state, Colorado BioScience Association leads expansion policies to advance the industry and accelerate growth. We support a thriving bioscience sector by connecting innovators to funding, infrastructure, research and talent. CBSA fosters bioscience workforce and leadership development through opportunities for networking and professional education.


    Drug Development & Delivery

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    Drug Development & Delivery is a print/online content provider that presents the latest scientific methods in drug development for professionals.


    ONdrugDelivery Magazine

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    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.


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    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.


    Farmavita

    Supporters
    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!


    GBI

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    http://www.gbihealth.com/

    GBI is an information, applications, and services company focused on the healthcare industry. Leveraging data from across the healthcare value chain, GBI creates web and mobile applications that enable individuals and organizations to make better decisions and communicate more effectively.


    Pharmacircle

    Supporters
    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….


    Pharmavision

    Supporters
    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.


    Inderscience Publishers

    Supporters
    http://www.inderscience.com

    Inderscience is a dynamic, leading, independent journal publisher. The company disseminates the latest research across the broad fields of science, engineering and technology; management, public and business administration; environment, ecological economics and sustainable development; computing, ICT and internet/web services, and related areas. Inderscience offers over 35 years' experience in publishing and has succeeded in building a substantial collection approaching 400 high-quality peer-reviewed international research journals in both online and print formats. We offer a variety of ways to keep up-to-date with the latest published leading-edge research while our online collection represents a fully-searchable digital archive of around 60,000 articles.


    Drug Target Review

    Supporters
    http://www.drugtargetreview.com

    Drug Target Review’s quarterly magazine, website and annual events program provides high quality content with peer-written articles that are submitted exclusively by the world’s most respected scientists in their field. This attracts a committed base of readers, users and delegates made up of senior decision-makers from the life science and drug discovery industries at the top pharmaceutical companies, as well as academics and scientists from the top research institutes across the globe.


    International Pharmaceutical Industry

    Supporters
    http://www.ipimediaworld.com

    IPI gives you an insight into all areas of Biopharm, Medical, Pharmaceutical and Healthcare. IPI provides a proven supportive means of communication to the Pharmaceutical, Bio Pharmaceutical, Nutraceutical and Medical Devices industry, incorporating the latest in research and technology innovations, regulatory guidelines, marketing and communication strategies.


    Swiss Biotech Association

    Supporters
    http://www.swissbiotech.org/

    The Swiss Biotech Association (SBA) is the national industry association for biotechnology, including pharmaceuticals, diagnostics, agriculture, food, cosmetics, environmental biotechnology, and specialty chemicals. Members are companies active in modern biotechnology, such as R&D, Production, Marketing and Sales, Finance, Services and Consulting. SBA provides a networking platform for Life Science clusters, academic and federal institutions the like. Founded in March 1998, the Association grows steadily.


    Copybook - Pharmaceutical

    Supporters
    http://www.copybook.com/pharmaceutical

    Copybook is a global business network with many pharmaceutical events, exhibitions and seminars. We encourage business-to-business transactions and work tirelessly to gain our customers new business contracts worldwide. You can add events, companies and associations for free. When you are a member, you can add your company to the events listed in order to encourage other visitors to arrange meetings and appointments at those events to facilitate new business contracts. Want to see how we can increase your business network and transactions? SIGN UP FOR FREE today! Copybook – Your Global Business Network


    Pharmalicensing

    Supporters
    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.


    Pharmaceutical-tech.com

    Supporters
    http://www.pharmaceutical-tech.com/

    Pharmaceutical-Tech : “In the realm of Pharmacy, where innovation is rapid, Pharmaceutical-Tech stands adept at conceptualizing unique ideas relevant to the B2B space. Pharmaceutical-Tech is essentially a B2B online business, technology media platform and global magazine that have under its wraps the largest global database of Pharmacy buyers and suppliers. Pharmaceutical-Tech.com covers in-depth trends that shape industry dynamics and metamorphose global economics. With services like search engine optimization, global magazine, social media marketing, product video showcase, e-mail marketing, e-newsletter sponsorship, banner advertising, event marketing and micro-website within our platform, www.pharmaceutical-tech.com has created a recognition that spans over a global audience, thereby revolutionizing how businesses transact.”


    Packaging-gateway

    Supporters
    http://www.packaging-gateway.com

    Packaging executives from around the world use the website to keep abreast of the latest industry developments and make informed purchasing decisions along the entire supply chain. Packaging-gateway.com provides up-to-date industry intelligence through: •Regularly updated news bulletins and company press releases •Feature articles written by leading industry figures •Detailed research reports containing the latest market statistics •The latest packaging related projects •White papers containing the latest analysis, insights and technology solutions


    Pharmaceutical Outsourcing

    Supporters
    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.


    Absave

    Supporters
    http://www.absave.com

    Absave.com is the leading savings website for Antibodies and Immunological Products. Search our extensive database of Antibodies, Kits, Proteins & Peptides, Reagents, etc. to find the best savings!


    Drug Development Technology

    Supporters
    http://www.drugdevelopment-technology.com

    Drugdevelopment-technology.com covers every aspect of the drug development and research process, from conception to pre-FDA approval. Our global network of journalists updates the site with the latest and most significant industry developments. This coverage allows us to provide everyone - from senior management through to research and QA staff – with in-depth reviews of the latest projects, advance notice of new product releases and analysis of the latest procedural and legislative developments.


    Labsave

    Supporters
    http://www.labsave.com

    Labsave is the leading savings website for Laboratory Equipment and Lab Supplies. We work closely with the top suppliers in the world to bring you the best products at the most competitive prices. We are constantly striving to secure the biggest and most exclusive offers that you won’t find anywhere else! http://www.labsave.com/


    Mednous

    Supporters
    http://www.MedNous.com

    MedNous is a print publication and website about medical innovation in Europe. It carries exclusive interviews with companies that are at the forefront of medical technology, as well as contributor articles from prominent practitioners. Our mission is to identify significant advances in medicine and to explain how this innovation is being commercialised. In doing so, we talk to venture capitalists about what products and platforms they are supporting. We report on how regulators cope with the accelerating pace of innovation. And we regularly cover the latest developments in the discovery and development of new medical concepts in the area of antibodies, vaccines, small molecules, regenerative medicine and nanomedicines. MedNous combines the English word for medicine with the Greek word for intellect. And those with nous are readers of our publication. Visit our website: www.mednous.com


    Labhoo

    Supporters
    http://www.labhoo.com


    Hyatt Regency Mission Bay

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    USA

    Hyatt Regency Mission Bay

    Experience the epitome of California coastal chic at Hyatt Regency Mission Bay Spa and Marina San Diego vacation resort near SeaWorld San Diego. Expect the best at this remarkable San Diego vacation resort offering incredible ocean views, waterfront dining, a contemporary poolside lounge, eco-friendly spa, and redesigned hotel rooms and suites and meeting rooms. The only resort hotel in San Diego with multiple water slides, you'll delight in a water playground with three new pools, waterfront health club, and a full-service marina with jet skis, sailboats, kayaks, sportfishing and whale excursions.

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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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