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Pre-Filled Syringes

Emulating on the success of 7th annual event, SAE Media Group is proud to announce the return of the elite 8th annual Pre-Filled Syringes meeting to London in 2016! 

The device and drug delivery market is continuing to grow exponentially with the likes of pre-filled pen systems, auto-injectors and patch pumps continuing to pave the way to enhancing drug delivery of biologics. Figures show that despite challenges relating to drug stability, manufacturing and competition from other drug delivery technologies, the market is poised for significant growth in the coming years and will account for nearly $6 Billion in revenue by the end of 2020.*

 

 Although glass continues to remain the gold standard for pre-filled syringes, the proportion of plastic based pre-filled syringes is expected to increase by 5% between 2015 and 2020*, due to concerns of glass breakage and plunger failure. It’s time to start reviewing packaging and device design in more depth, from technology and market drivers to challenges and strategies within the supply chain.

Mark your calendar to RSVP for this most sought-after event!

*http://www.prnewswire.com/news-releases/the-pre-filled-syringes-market-2015---2030---opportunities-challenges-strategies--forecasts-300016543.html

FEATURED SPEAKERS

Alphons Fakler

Alphons Fakler

Senior Packaging Manager, Novartis Pharma AG
Dominique Lavergnat

Dominique Lavergnat

Device Development Engineer, F Hoffmann -La Roche Inc
Jean-Rene Authelin

Jean-Rene Authelin

Global Head of Pharmaceutical Engineering, Sanofi R&D
Paul Kinsey

Paul Kinsey

Product Leader – Visual Inspection & Leak Detection, GSK
Stephen Barat

Stephen Barat

Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan

Adrien Tisserand

Category Manager-Parenteral, Nemera
Adrien Tisserand

Alphons Fakler

Senior Packaging Manager, Novartis Pharma AG
Alphons Fakler

Andreas Kerschbaumer

Facilitator Filling & Inspection, Sandoz
Andreas Kerschbaumer

Bigdeli Soltani Maedeh

Production Manager (Aseptics), Barts Health Pharmaceutics
Bigdeli Soltani Maedeh

David Blakey

Device Engineering, GSK R&D
David Blakey

Dietmar Engels

Vice President R&D Projects, West Pharmacuetical Services
Dietmar Engels

Dominique Lavergnat

Device Development Engineer, F Hoffmann -La Roche Inc
Dominique Lavergnat

Dragana Cvijanovic

Worldwide Strategic Marketing Leader, BD Medical - Pharmaceutical
Dragana Cvijanovic

Ee Li

R&D Technical Specialist, The Royal London Hospital
Ee Li

Jean-Rene Authelin

Global Head of Pharmaceutical Engineering, Sanofi R&D
Jean-Rene Authelin

Juha Mattila

Senior Product Manager, STERIS Corporation
Juha Mattila

Juha Mattila is Senior Product Manager for STERIS Finn-Aqua High Purity Water & Steam, VHP Sterilization and Effluent Decontamination systems. He joined Steris Finn-Aqua in 2000 as process / mechanical engineer and has broad experience in the design and manufacturing of pharmaceutical and research process equipment, with several years in Research and Development department, directly involved in the development & design of STERIS Finn-Aqua products and process systems. He has worked directly with several clients in the designs and installations in Europe, North America and Asia, presented in several events, and contributed as author/co-author for articles in professional journals.

Koller Horst

CEO, HK Packaging Consulting GmbH
Koller Horst

Mark Chipperfield

Director & Principal Consultant, Corvus Device Limited
Mark Chipperfield

Paul Kinsey

Product Leader – Visual Inspection & Leak Detection, GSK
Paul Kinsey

Richard Featherstone

Managing Director, Medical Device Usability Ltd
Richard Featherstone

Shun Ogawa

Research Manager, Mitsubishi Gas Chemical Company Inc.
Shun  Ogawa

Stephen Barat

Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan
Stephen Barat

Stephen Morley

Vice President, Sales and Service, Noxilizer, Inc.
Stephen Morley

Valerie Fenster

Sr. Manager Human Factors Engineering, Amgen
Valerie Fenster

Vikas Jaitely

Senior Pharmaceutical Assessor, MHRA
Vikas Jaitely

William Dierick

Director Technology Development, Terumo Europe
William Dierick
  • Stephen Barat, Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan
  • Jean-Rene Authelin, Global Head, Pharmaceutical Engineering, Sanofi R&D
  • Frank Dominique, Senior Device Development Engineer, F.Hoffmann-La Roche Ltd.
  • Paul Kinsey, Product Leader – Visual Inspection & Leak Detection, GSK
  • Valerie Fenster, Sr. Manager, Human Factor Engineering, Amgen
  • Vikas Jaitley, Deputy Manager & Pharmaceutical Assessor, Licensing Division, MHRA
  • Maedeh Bigdeli Soltani, Production Manager, Barts Health NHS Trust

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Workshop Leader's Opening Remarks

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9:10

Development of a PFS-System

  • A holistic plan and considerations from vial to a PFS
  • Latest advancements in secondary packaging system and what needs to be aware of?
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    10:30

    Morning Coffee

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    11:00

    Regulatory Aspects - It’s Not Just About Compliance

  • Classification of PFS
  • Everyone’s talking about extractables and leachables but what are they and how to demonstrate data?
  • Testing requirements and who should be in charge?
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    12:30

    Workshop Leader's Closing Remarks and Close of Day One

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    13:30

    Registration & Coffee

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    14:00

    Workshop Leader's Opening Remarks

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    14:10

    Understanding Formulation of Drug Early On

  • Stability of formulation for PFS
  • Injection time and force on stability of drugs
  • Flow rate, glide force and penetration force modeling - how to relate this to device design?
  •  

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    15:30

    Afternoon Tea

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    16:00

    Should We Switch to Auto Injectors (AI)?

  • From science to commerciality to stability - pros and cons of AI
  • Safety concerns and interaction with drug delivery
  • Manufacturing challenges for PFS vs. AI - from environment to fill/finish technology
  • Decision - how and when should we choose AI?
  • Comparison with other alternative/non-invasive drug delivery options
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    17:00

    Q&A - Discussion

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    17:30

    Workshop Leader’s Closing Remarks and End of Workshop

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Alphons Fakler

    Alphons Fakler, Senior Packaging Manager, Novartis Pharma AG

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    9:10

    How Do Patient-Needs Drive an Efficient Device Development Process?

    David Blakey

    David Blakey, Device Engineering, GSK R&D

  • Design inputs that inform and direct decisions
  • Unmet patient-needs that drive development
  • Concept selection in a crowded and competitive device technology market
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    9:50

    Multi-Layer Plastic Syringe for Oxygen-Sensitive Drug

    Shun  Ogawa

    Shun Ogawa, Research Manager, Mitsubishi Gas Chemical Company Inc.

  • Prevent oxidation of medicinal solution
  • Low protein (medicinal solution) adsorption
  • Low silicone pre-fillable syringe
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    10:30

    The Path to Enhancing Medical Devices from Pre-Filled Syringes to Auto Injectors

    Jean-Rene Authelin

    Jean-Rene Authelin, Global Head of Pharmaceutical Engineering, Sanofi R&D

  • The physics involved
  • Modelling of the AI, IJT distribution
  • Estimation of the variability
  • Impact of the design methodology
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    11:10

    Morning Coffee & Networking Break

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    11:40

    The Update of Biologics, A Rising Demand for Innovative Safety Systems

    Adrien Tisserand

    Adrien Tisserand, Category Manager-Parenteral, Nemera

  • Homecare and biologics, a growing trend in parenteral
  • What technical challenges does it raise?
  • Review of innovative safety solutions
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    12:20

    REAL LIFE CASE STUDY: Assessing How to Reduce Risks by Design Instead of Introducing Controls

    Valerie Fenster

    Valerie Fenster, Sr. Manager Human Factors Engineering, Amgen

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    13:00

    Networking Lunch

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    14:00

    Review Usability Challenges of PFS and How Human Factor Study Can Support the Setting of Specification and Selection of a Rigid Needle Shield (RNS) Design

    Dominique Lavergnat

    Dominique Lavergnat, Device Development Engineer, F Hoffmann -La Roche Inc

  • Usability of combination products as a key factor for self-administrated drug – challenges for PFS
  •  How human factor study can support and define design inputs?
  •  Patient group study to assess performances of RNS on outer design to reduce usability risks
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    14:40

    Human Factors (HF) Testing of Pre-Filled Syringes (PFS)

    Richard Featherstone

    Richard Featherstone, Managing Director, Medical Device Usability Ltd

  • What do regulators want from HF data?
  • If I am using an existing PFS, what HF data do I need to generate?
  • HF validation studies for PFS - top tips
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    15:20

    COP Polymer-Based Pre-Filled Syringes and the Merits for Sensitive Therapeutic Proteins

    William Dierick

    William Dierick, Director Technology Development, Terumo Europe

  • Importance for minimising risks of protein interaction with surfaces and materials of the container closure system to eliminate immunogenicity and ensure drug safety and efficacy
  •  A COP pre-fillable syringe system specifically designed to mitigate risk of protein degradation
  • A system approach, including various aspects: contact materials, silicone-oil free system, applied method of sterilisation
     
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    16:00

    Afternoon Tea & Networking Break

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    16:30

    Designing for Sterilisation: Materials, Packaging and Other Considerations

    Stephen Morley

    Stephen Morley, Vice President, Sales and Service, Noxilizer, Inc.

  • Sterilisation methods, with focus on temperature sensitive products
  • Material and packaging selection
  • Regulatory aspects of using novel, non-traditional sterilization methods
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    17:10

    Panel Discussion

  • How can we enhance devices to reduce needle stick injuries?
  • What necessary steps should be taken to ensure a successfully and safe PFS for end users?
  • Reviewing protection mechanisms for consideration to prevent needle stick injuries

     

  • Alphons Fakler

    Alphons Fakler, Senior Packaging Manager, Novartis Pharma AG

    Richard Featherstone

    Richard Featherstone, Managing Director, Medical Device Usability Ltd

    Mark Chipperfield

    Mark Chipperfield, Director & Principal Consultant, Corvus Device Limited

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    17:50

    Chairman’s Closing Remarks and Close of Day One

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Stephen Barat

    Stephen Barat, Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan

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    9:10

    Prefilled syringes: Understanding the Regulatory Challenges

    Vikas Jaitely

    Vikas Jaitely, Senior Pharmaceutical Assessor, MHRA

  • Prefilled syringes regulated as a medicinal product or a medical device in EU (combination products - definitions and examples)
  • Regulatory pathways and data expected in the registration dossier
  • Usability studies - human factor engineering
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    9:40

    Q&A For the Regulator

    Vikas Jaitely

    Vikas Jaitely, Senior Pharmaceutical Assessor, MHRA

    Delegates can ask the representative questions in this interactive session to gain a better understanding of regulators' expectations and requirement

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    9:50

    New Technologies and Market Trends for Cartridge Components

    Dietmar Engels

    Dietmar Engels, Vice President R&D Projects, West Pharmacuetical Services

  • Market overview for container solutions
  • Cartridges, a packaging solution used for biological drugs
  • Cartridge components and next generation component development - functional, chemical and quality requirements
  • Nested ready to use cartridge solutions
  • New machine concepts - all in one
  • Applications and delivery devices in combination with cartridges
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    10:30

    Morning Coffee

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    11:00

    Conducting thorough Visual Inspection and Catching the Problem before Recall

    Paul Kinsey

    Paul Kinsey, Product Leader – Visual Inspection & Leak Detection, GSK

  • Overview of requirements and regulatory expectations
  • Certification, qualification and validation
  • Practical considerations for 'difficult to inspect' products
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    11:40

    Next-Generation, High-Performance Polymer Syringe

    Dragana Cvijanovic

    Dragana Cvijanovic, Worldwide Strategic Marketing Leader, BD Medical - Pharmaceutical

  • How introducing 'simulated studies' during the development of large volume polymer prefillable syringes can help gain development time
  • A robust data package to support market authorization application: Design control, HF engineering and clinical studies
  • How an original regulatory approach can assist with securing drug regulatory pathway
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    12:20

    Networking Lunch

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    13:20

    Process, Aseptic Manufacturing Applications, Cycle Development and Validation of VHP Low Temperature Terminal Surfaces Sterilisation

    Juha Mattila, Senior Product Manager, STERIS Corporation

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    14:00

    Filling Accuracy as a Key Concern to be Reviewed

    Andreas Kerschbaumer

    Andreas Kerschbaumer, Facilitator Filling & Inspection, Sandoz

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    14:40

    Afternoon Tea

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    15:10

    Safety Assessment of Leachables When Developing Pre-Filled Syringes Drug Products

    Stephen Barat

    Stephen Barat, Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan

  • An overview of leachables and need for safety assessment will be presented
  • Current best practices for safety evaluation as related to the development of a pre-filled syringe combination drug product will be discussed with examples
  • Final PQRI best practice recommendations for leachable safety assessment will be covered
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    15:50

    Keynote Address: Aseptic Services in the NHS

  • Overview of aseptic services provided
  • Dose banding and the future of aseptic services for NHS
  • Requirements of PFS and validation

     

  • Bigdeli Soltani Maedeh

    Bigdeli Soltani Maedeh, Production Manager (Aseptics), Barts Health Pharmaceutics

    Ee Li

    Ee Li, R&D Technical Specialist, The Royal London Hospital

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    16:30

    Panel Discussion

    Stephen Barat

    Stephen Barat, Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis, Allergan

  • Zero tolerance - how to ensure complete sterile operating environment?
  • Assessing logistics' impact on PFS and drug stability for intended markets
  • What if? Preparing for the worst and contamination: How to manage the risks and what is the contingency plan?

    Panel will be joined by speakers of the day

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    17:00

    Chairman’s Closing Remarks and Close of Day Two


    Category Manager-Parenteral
    Nemera
    Senior Packaging Manager
    Novartis Pharma AG
    Facilitator Filling & Inspection
    Sandoz
    Production Manager (Aseptics)
    Barts Health Pharmaceutics
    Device Engineering
    GSK R&D
    Vice President R&D Projects
    West Pharmacuetical Services
    Device Development Engineer
    F Hoffmann -La Roche Inc
    Worldwide Strategic Marketing Leader
    BD Medical - Pharmaceutical
    R&D Technical Specialist
    The Royal London Hospital
    Global Head of Pharmaceutical Engineering
    Sanofi R&D
    Senior Product Manager
    STERIS Corporation
    CEO
    HK Packaging Consulting GmbH
    Director & Principal Consultant
    Corvus Device Limited
    Product Leader – Visual Inspection & Leak Detection
    GSK
    Managing Director
    Medical Device Usability Ltd
    Research Manager
    Mitsubishi Gas Chemical Company Inc.
    Executive Director, Non-Clinical & Translational Sciences, Safety Assessment & Bioanalysis
    Allergan
    Vice President, Sales and Service
    Noxilizer, Inc.
    Sr. Manager Human Factors Engineering
    Amgen
    Senior Pharmaceutical Assessor
    MHRA
    Director Technology Development
    Terumo Europe

    Sponsors and Exhibitors

    Online Partner

    Supporters

    Pre-Filled Syringes East Coast USA

    Download

    Pre-Filled Syringes 2016 Preliminary List of Attendees

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    SMi Speaker Interview Series: Horst Koller, HK Packaging Consulting GmbH

    Download

    SMi Speaker Interview Series: William Dierick, Director of the Technology Development – Global Pharmaceutical Solutions, Terumo

    Download

    SMi Speaker Interview Series: Juha Mattila is Senior Product Manager, STERIS FINN-AQUA

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    SMi Speaker Interview Series:Stephen Morley, Vice President, Sales and Service, Noxilizer Europe

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    SMi Speaker Interview Series: Richard Featherstone, MD, Medical Device Usability

    Download

    Sponsors and Exhibitors


    3P Innovation

    Sponsors and Exhibitors
    http://www.3pinnovation.com

    3P provides device development and custom automation that help customers de-risk and commercialise faster at lower cost. We manufacture scalable machines, from lab-scale to full-scale production for sterile processing, powder and liquid fill-finish, assembly and test. Specialists in novel primary drug containers, reconstitution, wearable devices, auto-injectors, depots, cartridges and specials.


    AAF International

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

    Based on its strong history, continuous investments in R&D and commitment within the industry, AAF has built significant expertise in clean air solutions. The product and service portfolio comprises a complete range of filters for solid particles and gaseous molecular substances. All products are tested according to EN779:2012 and EN1822:2009.


    BD Medical

    Sponsors and Exhibitors
    http://www.drugdeliverysystems.bd.com

    As a partner of choice for the pharmaceutical and biotech companies across the globe, BD Medical - Pharmaceutical Systems provides a broad range of ready-to-use drug delivery systems including glass and plastic prefillable syringes, safety and shielding systems, self-injection systems and connected solutions that help ensure smooth delivery, regardless of drug complexity, viscosity and dosing volume.

    With an unbending emphasis on innovation and the highest level of technical expertise, BD Medical - Pharmaceutical Systems provides pharmaceutical and biotechnology companies with support and resources to help them achieve their goals. We support their product launch and life cycle management through sophisticated consultative, analytical and clinical services to help ensure drug compatibility and seamless systems integration, while accelerating time-to-market and reducing risk.

    More information available @ drugdeliverysystems.bd.com



    Medical Device Usability

    Sponsors and Exhibitors
    http://www.medical-device-usability.com/

    Medical Device Usability is an independent human factors/usability testing consultancy offering a turn-key service. MDU plans and performs formative and summative evaluations for a wide range of medical technologies, including prefilled syringes, pen injectors and autoinjectors. MDU tests globally for some of the world’s largest pharmaceutical and medical device companies.


    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.


    Noxilizer

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

    Noxilizer, Inc. provides room temperature nitrogen dioxide sterilization technology. NO2 sterilization has shorter cycles (approximately 2 hours including aeration), operates with or without vacuum and is easily installed—an ideal solution for prefilled syringes and drug-device combination products. Noxilizer provides contract sterilization services and sells sterilization and decontamination equipment. The company has offices in the US, UK & Japan.


    Owen Mumford

    Sponsors and 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.


    STERIS

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

    STERIS Life Sciences is your trusted partner in contamination control. For over 100 years, STERIS has been a global leader and expert in the industries of sterilization, cleaning and infection control.

    Today, we continue to build on this heritage by providing the products and resources you need throughout every step of your process. From innovation to results, our comprehensive portfolio of products and services is designed to meet your needs.

    With offices located worldwide and technicians in over 100 countries, you can count on us to be where you are when you need us, every step of the way. Trust STERIS Life Sciences to help you create a healthier and safer world.



    Team Technik

    Sponsors and Exhibitors
    http://www.teamtechnik.com/en/medtech/medtech/

    Headquartered near Stuttgart, Germany, teamtechnik is an established global provider of turnkey assembly, handling and testing systems for medical devices. The expertise encompasses device development and industrialization support. Based on industry best practices, scalable TEAMED platforms, produce at up to 140 cycles/minute.


    Terumo

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

    Terumo Corporation is one of the world’s leading medical technology companies and operates in more than 160 nations. Terumo, founded in 1921, develops, manufactures and distributes a broad range of world-class medical devices including the supply of drug delivery/injection devices to the pharmaceutical industry. Terumo Global Pharmaceutical Solutions (GPS) 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.


    West Pharmaceutical Services

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

    West Pharmaceutical Services, Inc., is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products. Working by the side of its customers from concept to patient, West creates products that promote the efficiency, reliability and safety of the world's pharmaceutical drug supply. West is headquartered in Exton, Pennsylvania, and supports its customers from locations in North and South America, Europe, Asia and Australia.


    Zwick Testing Machines

    Sponsors and Exhibitors
    http://www.zwick.co.uk

    Zwick Roell has extensive experience designing and supplying apparatus for testing medical products. Generally, testing products installed in this sector are customised designs incorporating fixtures adapted to suit the medical device being evaluated. Zwick ‘testXpert’ software provides testing functions and detailed documentation to facilitate validation in this heavily regulated sector.

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    FierceBiotech is the biotech industry's daily monitor. Biotech executives rely on FierceBiotech to stay up to speed on biotech corporations, FDA approvals & regulations, industry mergers & acquisitions, clinical trials, and more. Beyond the news of the day, our editors produce in-depth features on industry leaders and up-and-comers, the regulatory environment, and market trends. In addition to our comprehensive website and free email newsletter, you have the opportunity to attend our webinars, peruse our whitepaper library and benefit from our eBooks. Advance your career through our exclusive networking parties and life sciences job board.

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    Medicaldevice-network.com is your one stop for information on the medical device industry, covering everything along the supply chain from biomaterials and materials solutions to electronics, packaging, motors and motion control, outsourcing and more. Through our international team of journalists, we cover diagnosis, prevention, monitoring, standards, treatment and technology – all you need as a professional in the medical industry to stay abreast of the latest developments in your field.


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    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!


    GenomeWeb

    Supporters
    http://www.genomeweb.com

    GenomeWeb LLC is an independent, privately-held online and print publisher based in New York. Since 1997, GenomeWeb has served the global community of scientists, technology professionals, and executives who use and develop the latest advanced tools in molecular biology research and molecular diagnostics.

    GenomeWeb’s editorial mission is to serve readers with exclusive, in-depth coverage of the technology, institutions, and scientists that make up the worldwide research enterprise of molecular biology. We operate the largest online news organization focused on advanced research tools in genomics, proteomics, and bioinformatics.

    GenomeWeb readers can be found in major biopharmaceutical companies, top research universities, biomedical institutes, and government laboratories.


    CanBiotech

    Supporters
    http://www.canbiotech.com

    CanBiotech - A Portal and B2B Outsourcing Marketplace for the Biotech and Pharmaceutical Industry. The Marketplace features the Outsourcing Services Showcase; the Portal features our biopharmaceutical and venture capital directories and databases. Publications include the BioMedical Outsourcing Report and the Bio Outsourcing Asia© Publication.


    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


    pharmaphorum

    Supporters
    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


    Samedan

    Supporters
    http://www.samedanltd.com/magazine/13.

    International Clinical Trials (ICT) is a quarterly magazine edited by Dr Graham Hughes, and written by specialists at the forefront of clinical research. ICT’s coverage of operational developments ranges from adaptive designs in early phase trials through to post marketing research. ICT’s targeted readership consists of key decision makers across the pharmaceutical and biotech industries, along with contract partners and consultants. The magazine is distributed to pharmaceutical professionals in Europe and North America, and is accessed globally online. Read the latest issues, explore the ICT archive and subscribe at www.samedanltd.com/magazine/13.


    Biosave

    Supporters
    http://www.Biosave.com

    Biosave.com brings together the best Life Science promotions, product releases, featured products, publications, videos and events from 100’s of leading Life Science suppliers. Updated 24 hours a day, Biosave is constantly uploading special promotions and exciting product news that you won’t find anywhere else. Our goal is to provide our users with the most exclusive product information to help reach that all important purchasing decision.


    Int. J. of Biotechnology

    Supporters
    http://www.inderscience.com/ijbt

    IJBT provides an international forum and refereed authoritative source of information in the field of Biotechnology and Biotechnics, with emphasis on management and economics, as well as the political and social issues. It aims to disseminate knowledge, provide a learned reference in the field, and establish channels of communication between academic and research experts, policy makers and executives in industry, commerce and investment institutions.


    Bentham ebooks - Biopolymers in Drug Delivery: Recent Advances and Challenges

    Supporters
    http://ebooks.benthamscience.com/book/9781608050789/

    Biopolymers in Drug Delivery: Recent Advances and Challenges describes the applicability of diverse natural and synthetic biopolymers and their blends in drugs, vaccines and gene delivery. It would serve as a concise body of information on biopolymers for researchers, industries and students of pharmaceutical, chemical, engineering and biomedical sciences. Practical and theoretical concepts are presented in depth. Examples of yet untapped indigenous African polymers with drug delivery potentials are highlighted. Many natural biopolymers with excellent drug delivery properties have not been appropriately exploited because there is very concise body of information that would demonstrate their potential. This Ebook should prove to be an important resource to researchers in the field.


    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.


    Gate2Biotech

    Supporters
    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.


    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.


    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.


    PMR

    Supporters
    http://www.pmrcorporate.com

    PMR (www.pmrcorporate.com) is a British-American company providing market information, advice and services to international businesses interested in Central and Eastern European countries as well as other emerging markets. PMR's key areas of operation include business publications (through PMR Publications), consultancy (through PMR Consulting) and market research (through PMR Research ). Being present on the market since 1995, offering high international standards in projects and publications, as well as providing one of the most frequently visited and top-ranked websites, PMR is one of the largest companies of its type in the region.


    Antibodies Online

    Supporters
    http://www.antibodies-online.com

    antibodies-online.com facilitates researchers to find the appropriate antibodies for their respective research project. As an independent and multi-vendor marketplace for research antibodies and thanks to the cooperation with more than 130 different manufacturers, a large selection of Antibodies (over 700,000), ELISA Kits (over 130,000), Secondary Antibodies (17,000), Proteins (130,000), Peptides and Isotype Controls is available. By supporting the Independent Validation Initiative and the Resource Identification Initiative, antibodies-online.com also addresses the important topics of transparent product quality and scientific reproducibility. In addition scientists receive news and detailed information about the individual antibodies from databases such as the PubMed and others.


    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!

    Copthorne Tara Hotel

    Scarsdale Place
    Kensington
    London W8 5SR
    United Kingdom

    Copthorne Tara Hotel

    The Copthorne Tara Hotel London Kensington is an elegant contemporary four-star hotel in prestigious Kensington, located just a two minutes walk from High Street Kensington underground station, making exploring easy. The hotel offers well-appointed and comfortable guest rooms combining Standard, Superior and Club accommodation. Club rooms offer iconic views over the city and include Club Lounge access for complimentary breakfast and refreshments. Guests can sample the authentic Singaporean, Malaysian and Chinese cuisine at Bugis Street, traditional pub fare at the Brasserie Restaurant & Bar or relax with a delicious drink at West8 Cocktail Lounge & Bar.

    The Copthorne Tara Hotel boasts 745 square meters of flexible meeting space, consisting of the Shannon Suite and the Liffey Suite, ideal for hosting conferences, weddings and social events. Facilities include access to the business centre 24 hours a day, fully equipped fitness room, gift shop, theatre desk and Bureau de Change. With ample onsite parking outside the London congestion charge zone and excellent transport links via Heathrow Airport, the hotel is the perfect location for business or leisure stays. The hotel is within close proximity to the shops of High Street Kensington, Knightsbridge and Westfield London, Olympia Conference Centre, Royal Albert Hall, Kensington Palace and Hyde Park.

     

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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
    Registered in England - SMi Group Ltd trading as SAE Media Group




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