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Pre-Filled Syringes & Injectable Drug Devices
16 January - 17 January 2019
Pre-Filled Syringes & Injectable Drug Devices

The global prefilled syringes market size is expected to reach a value of $22.5 billion USD by 2025 with growing usage of prefilled syringes and technological advancements in auto-injectors being the key factors driving the market.


With that in mind, SAE Media Group is proud to present the 11th Annual European Pre-Filled Syringes Conference, taking place on the 16th-17th of January 2019, in London.


As Europe’s leading PFS conference, we will explore new technologies and innovations for platform systems of injectable delivery devices, and assess the impact of digitalisation, patient-centricity and the regulatory compliance which make up such core components within the PFS sphere.


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 January.
 

This is our most sought-after event and will be sold out soon.
Early registration is strongly advised to avoid disappointment.
 

FEATURED SPEAKERS

Justin Wright

Justin Wright

Global Head of Innovation, Novartis
Michael Becker

Michael Becker

Design Engineer, Boehringer Ingelheim
Veronika Ganeva

Veronika Ganeva

Biologicals Quality Assessor , MHRA

Alexander Zuern

Device Testing Manager, Novartis
Alexander Zuern

Alexander Zürn is a pharmacist by training. He got a PhD in Pharmacology from the University of Würzburg, Germany and did a postdoc at the University of California Berkeley at the department of bioengineering. From there he joined Novartis in 2012 as a process expert. From the production he join the QC Department of Novartis Stein and was until 2017 a QC team leader and SPOC for the injectable device testing at the release site.
Since 2017 he has been in the Device Development and Commercialization (DD&C) department at Novartis Basel as a device testing manager and is the Analytics and Testing Network leader.
 

Anil Busimi

Strategy and Innovation Global Product Manager, SCHOTT
Anil Busimi

Anil Busimi started his professional career in 2003 at SCHOTT AG in Germany. He worked in different roles including business development, project manager, and consultant in corporate strategy. In 2005, he moved to SCHOTT Pharmaceutical Packaging business and played a key role in building long-term business strategy with sound understanding of market trends, customer needs and competitive landscape. He has more than 10 years experience in product management and innovation. From August 2009 until June 2016, he held various positions in global product management for pre-fillable syringe business including glass and polymer PFS solutions. Currently, he is in the strategy & innovation team as senior global product manager for Cartridges and led the iQ™ Platform market launch. He is a professional speaker at many conferences and seminars on topics related to parenteral primary packaging and drug delivery devices.
He holds M.Sc. degree in Agriculture and Genetics and a MBA
 

Davide Mercadante

Sr Associate Quality Drug Devices, Biogen
Davide Mercadante

Davide Mercadante is a medical engineer with 10+ years of experience within multiple areas of device and combination product development, including design & development, design quality assurance, verification & validation engineering, quality control and supply chain quality. He received his bachelor’s and master’s degree in medical engineering from the Second University of Rome, where is focus was on medical device design and development.
Davide has a Lean Six Sigma Green Belt and he currently works at Biogen in the Device Development Quality group where he is the quality project lead for both the Risk Management Continuous Improvements and Combination Product DHF 21CFR Part 4 Final Rule enhancement projects. He also has been instrumental with the integration of software as a medical device into the existing Quality Management System.
 

Elise Legendre

Head of Late stage PFS Development, Sanofi
Elise Legendre

With 15 years of experience across pharma, Elise currently serves as Head of late stage development of primary container in medical device at Sanofi.
She is responsible of leading the drug integrated product development for both biologics and small molecules on prefilled syringe based delivery system. Her group is mainly leading the operation of the PFS development and the transfer of the developed container and safety system to R&D center and manufacturing groups. Before this position, she was supporting various medical devices combination products, such as auto injectors, prefilled syringes projects as PFS expert and project manager.

Prior joining Sanofi, Elise was GSK’s packaging head on an industrial site in Normandy. She was managing the LCM activities on primary, secondary packaging.
Before this, Elise worked in Aseptic and Packaging manufacturing area as operational manager where she served in various roles focused on manufacturing, product commercialization and operational excellence.
 

James Mellman

Device Manager, Novartis
James Mellman

James is a device manager for Novartis in Basel, Switzerland. His main responsibilities include developing primary packaging systems for combination products and supporting new technologies. He has worked on a multitude of injection device platforms including pre-filled syringes, needle safety devices, auto injectors, and patch injectors. He has also helped to build and implement a renovated CCIT strategy for the Novartis Group. Before Novartis, James worked at Pfizer in their Devices Center of Excellence in Cambridge, UK (2008-2011) and Nutricia in their Advanced Medical Nutrition Division HQ in Amsterdam, NL (2011-2014). He received his PhD from the University of Florida in Materials Science & Engineering in 2007 specializing in biomaterials.

Justin Wright

Global Head of Innovation, Novartis
Justin Wright

With 20 years of experience across med tech and pharma, Justin currently serves as Global Head of Innovation at Novartis where he is responsible leading the enterprise innovation system across the drug development process for both biologics and small molecules. This includes activation of the innovation strategy and leading cross-functional innovation governance internally and externally to Novartis.

Prior to joining Novartis, Justin helped launch and then lead Lilly’s Cambridge Innovation Center that was tasked with building Lilly’s next generation delivery and connected product systems. This also included developing new innovation and external partnership models in order to accelerate drug delivery innovation along with mapping a number of strategies for digital biomarkers and clinical feedback loops. Before this, Justin worked at Becton Dickinson (BD) where he served in various roles focused on developing and commercializing drug delivery systems for the biotech, vaccine, and pharmaceutical industries. Justin began his career at Merck & Company working across manufacturing, product commercialization, and franchise management.

Justin holds a PhD in Bio-Organic chemistry from Clemson University and completed a research fellowship at Harvard Medical School. He is the author of more than 35 patents and publications.
 

Kim S. Halskov

Research Scientist, Novo Nordisk A/S
Kim S. Halskov

Kim S. Halskov is a research scientist at Novo Nordisk A/S. He did his studies at Aarhus
University, Denmark, in medicinal chemistry (BSc) and chemistry (MSc, PhD). He
received his PhD degree in synthetic organic chemistry 2015. In 2016 and 2017 he was a
postdoctoral researcher at Yale University in the field of synthetic organic chemistry.
Since 2018 he has been employed at Novo Nordisk A/S, where he is currently focused on
the application of nuclear magnetic resonance (NMR) spectroscopy analysis in various
aspects of the drug development process.

Lise Vanderkelen

Department Head, Nelson Labs NV
Lise Vanderkelen

Lise Vanderkelen received her Ph.D. from the Faculty of Bioscience Engineering at the University of Leuven (Belgium) in 2012. She started at Nelson Labs Europe (formerly known as Toxikon Europe) in 2013 as study director Extractables & Leachables, focusing on parenteral applications and in 2014 she became responsible for the chemical characterization testing of medical devices (ISO 10993-18). In 2016, she became Department Head Pharma Services at Nelson Labs Europe. The main focus of this team is identifying organic impurities in drug products as well as in-use stability for drug-device combinations. In 2017, the scope expanded and now she is also responsible for all microbiological as well as in-vitro toxicological testing at Nelson Labs Europe.

Markus Hemminger

Senior Device Engineer, Roche
Markus Hemminger

Markus Hemminger is a Senior Engineer who joined Roche in the year 2013, being a member of the prefilled syringe development, a subgroup of device development. Currently he is part of a cross-functional team developing a prefilled syringe for ocular injections where he is in charge of various tasks, e.g. designing and specifying the device components and planning of design verification. Before starting at Roche he was responsible for primary packaging development for biopharmaceuticals at Boehringer Ingelheim for more than 13 years. His main expertise includes selection, development and optimization of container closure systems like vials, cartridges and syringes, as well as transfer-and administration devices, packaging component related method- and process developments and CCI testing. Markus Hemminger studied chemistry at the University of Applied Sciences in Aalen, Germany.

Mathieu Rigollet

Senior PFS Engineer, Roche
Mathieu Rigollet

Mathieu is a graduated Mechanical Engineer from ENSAM Paris and furthermore holds a Master of Science in Biomedical Engineering. He has more than 12 years’ experience with primary packaging and medical devices. After obtaining his degree, Mathieu joined BD as a R&D Project Leader for non-sterile and sterile packaging projects. Beginning 2010, Mathieu took over the role of Senior R&D Engineer, where he had the responsibility for development activities around pre-fillable syringes. In June 2013, Mathieu joined the PFS Engineering Team at Roche.

He was responsible for primary packaging development in device teams for several molecules and he supported the technical development of the Platform Stacked-in-needle Syringe. Currently, Mathieu is the Device Team Leader for a molecule and is a leader of the Combination Product Control Strategy and of the Platform Pre-filled Syringe work streams.

Michael Becker

Design Engineer, Boehringer Ingelheim
Michael Becker


Dr. Michael Becker (1983) is working at Boehringer Ingelheim Pharma GmbH & Co. KG since 2016 as Design Engineer for parenteral combination products. Previously, he worked for 5 years at Sanofi-Aventis GmbH in the development of the same products. He studied Physics at the University of Mainz and wrote his PhD thesis about the „Development of an Aerodynamic Particle Model of Powder & Aerosols“ supervised by Mr. Prof. Cameron Tropea (Technical University Darmstadt) at Boehringer Ingelheim. In this time he specialized in writing simulations and statistics.

Michael Becker is married and lives together with his wife and his daughter near Mainz.
 

Nicolas Eon

Global Product Manager Glass PFS syriQ, SCHOTT
Nicolas Eon

Dr. Nicolas Eon, graduated from Universities of Nancy and Nantes, holds a Fluid Mechanics & Energy Science Engineering degree, a Master Degree in Energetics and Heat Transfer and a PhD. in Biomechanics. He worked for 10 years in the Automotive Safety Industry where he led the System Engineering Department in a global leading company. He has joined BD Pharmaceutical Systems in 2008 where he was in charge of the Global Product Engineering for Prefillable Syringe Systems. In 2012, Nicolas joined SCHOTT AG as Business Development Manager for Glass and Polymer Prefillable Syringes. Since 2010, he has been an active expert in ISO Technical Committees (ie. TC 76 WG4, TC 210) as part of the French and Swiss delegation. He is now in charge of the Glass PFS Strategy, Innovation and Technology Roadmap at SCHOTT AG as Global Product Manager for syriQ® brand.

Reinhard Scheller

Commercial Manager Cyclo Olefin Polymers - COP Europe, Zeon Europe GmbH
Reinhard Scheller

Professional Experience
2003 – present Commercial Manager Cyclo Olefin Polymers (COP) for Europe at Zeon Europe GmbH , Düsseldorf / Germany
• Responsible for the business development of Zeon’s Cyclo Olefin Polymers (COP) in Europe
• Focus on medical/pharmaceutical , analytical/diagnostical and optical COP applications

1996 – 2003 Sales Manager for Germany at Zeon Deutschland GmbH , Düsseldorf / Germany
1991 – 1996 Sales Representative Speciality Rubbers at Zeon Deutschland GmbH , Düsseldorf / Germany
1980 – 1991 Scientific co-worker at the Institut of Polymer Technology Dresden / Germany (today: Leibniz-Institute of Polymer Research Dresden)
Education
1975 – 1980 Studies of Materials Science (specialisation plastics technology and plastics processing) at Technical University Leuna-Merseburg / Germany
 

Severine Duband

Global Category Manager for Parenteral Segment, Nemera
Severine Duband

Séverine DUBAND has recently joined Nemera as Global Category Manager of the parenteral segment. She is responsible for developing the parenteral products, including the passive safety systems Safe’n’Sound®, the innovative autoinjector Safelia®, as well as several other projects.
Graduated from EM Lyon Business School in 2004, Séverine worked 10 years for FMCG in the chemical industry as International Category Manager, supervising strategic planning, NPD launches, project management and brand communication.
 

Shota Arakawa

Researcher , Mitsubishi Gas Chemical
Shota Arakawa

Mr. Shota Arakawa is a researcher of Advanced Business Development Division.
He gained a Diploma in Science in 2007 and a Master Degree of Science in 2009 from Osaka University.
Since April 2009 he has been working for Mitsubishi Gas Chemical Company, Inc.
and in charge of macromolecular science, especially in synthesis of polymers and material development.
Since 2012 he has joined a development team of multilayer plastic vial & syringe for biologics.

Steve Chamberlain

Device Engineering Manager, GSK
Steve Chamberlain

I lead the Late Stage Parenteral Engineering team within GSK’s Device Engineering department where I am responsible for the technical understanding, performance and robustness aspects of the parenteral devices within the late stage portfolio. I have a Masters degree in Mechanical & Manufacturing Engineering and, over a 13 year career at GSK, have held various positions, most notably as the Device Lead on GSK’s flagship dry powder inhalation device known as Ellipta.

Suraj Ramachandran

Director, MSD
Suraj Ramachandran

Suraj Ramachandran, MS, RAC, is a Director, Regulatory Affairs in the Drug Device Center of Excellence at Merck based in Rahway, NJ. Suraj is currently responsible for supporting various medical devices combination products, such as auto injectors, prefilled syringes, inhalers and contraceptives. In addition, he is heavily involved in providing guidance for digital solutions and has led many development efforts regarding medical device software, intended for both domestic and international markets. In previous roles within industry, he was responsible for an infusion pump platform as well as supporting all new product development and lifecycle maintenance activities including regulatory submissions, design control, audits, and CAPAs. Suraj holds a Master’s in biomedical engineering from the University of Michigan. In addition, he has earned the RAPS RAC certification.

Veronika Ganeva

Biologicals Quality Assessor , MHRA
Veronika Ganeva

Veronika is a quality assessor at the MHRA, where she is responsible for the evaluation of a diverse portfolio of biological medicinal products, which includes recombinant and non-recombinant proteins, monoclonal antibodies, plasma-derived products, vaccines, ATMPs and others. She has a PhD degree in Stem Cell and Developmental Biology from the University of Edinburgh and has worked on a range of research and regulatory positions in academia, the pharmaceutical industry and two regulatory agencies. Veronika is passionate about helping bring high quality medicinal products to the market and a fair and science-based regulatory process. She has an additional interest in medical devices and drug-device combination products.

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Opening Remarks and Introductions

Shannon E. Clark

Shannon E. Clark, Principal, UserWise, Inc.

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9:10

Session 1: Connected Devices and Digital Health - Current and Future Applications

  • What's the digital health landscape and latest buzz in Silicon Valley, California, as well as the rest of the world?
  • What innovations are currently tackling issues of medication adherence, medical product adherence, clinical decision-support, and remote patient monitoring?
  • How are innovators solving patient needs via user-centered design of digital health apps?
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    9:50

    Session 2: Overview of Applicable U.S. FDA Usability Engineering Requirements & Regulatory Requirements for Connected Devices and Digital Health

  • What U.S. FDA Regulations and Guidance do we need to know about when developing connected devices and digital health applications?
  • What digital health applications are NOT governed by the U.S. FDA
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    10:30

    Morning Coffee

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    11:00

    Session 3: Review Unique Usability Engineering Considerations Related to Connected Devices

  • Case Study: What are some unique human factors and usability engineering considerations when developing an app and connected device?
  • Case Study: What are some best practices and design considerations (i.e. heuristics) to take into account when developing digital health applications and connected devices?
  • Looking Ahead: What can we expect in 2029?
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    11:40

    Session 4: Q&A

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    12:20

    Closing Remarks and End of Workshop

    Shannon E. Clark

    Shannon E. Clark, Principal, UserWise, Inc.

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    13:30

    Registration & Coffee

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    14:00

    Opening Remarks and Introductions

    James Blakemore

    James Blakemore, Senior Consultant, Cambridge Consultants Ltd

    Sergio Malorni

    Sergio Malorni, Senior Consultant, Medical Technology, Cambridge Consultants Ltd

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    14:10

    Current Developments in the Body Worn Injector (BWI) Device Landscape

  • BWI Device Architectures
  • How these designs suit specific needs of pharma, users and other stakeholder
  • Notable examples of BWIs
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    14:50

    Holistic Review of Stakeholder Needs for New BWI-based therapies

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    15:30

    Afternoon Tea

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    16:00

    Understanding Future and Unmet Needs to Drive BWI Innovations

  • Patient-centric drivers
  • Clinical and therapy drivers
  • Market drivers
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    17:00

    Potential New BWI Technologies Developments

  • Primary Containers
  • Pump technologies
  • User interfaces
  • Connectivity
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    17:30

    Closing Remarks and End of Workshop

    Sergio Malorni

    Sergio Malorni, Senior Consultant, Medical Technology, Cambridge Consultants Ltd

    James Blakemore

    James Blakemore, Senior Consultant, Cambridge Consultants Ltd


    Device Testing Manager
    Novartis
    Strategy and Innovation Global Product Manager
    SCHOTT
    Sr Associate Quality Drug Devices
    Biogen
    Head of Late stage PFS Development
    Sanofi
    Device Manager
    Novartis
    Global Head of Innovation
    Novartis
    Research Scientist
    Novo Nordisk A/S
    Department Head
    Nelson Labs NV
    Senior Device Engineer
    Roche
    Senior PFS Engineer
    Roche
    Design Engineer
    Boehringer Ingelheim
    Global Product Manager Glass PFS syriQ
    SCHOTT
    Commercial Manager Cyclo Olefin Polymers - COP Europe
    Zeon Europe GmbH
    Global Category Manager for Parenteral Segment
    Nemera
    Researcher
    Mitsubishi Gas Chemical
    Device Engineering Manager
    GSK
    Director
    MSD
    Biologicals Quality Assessor
    MHRA

    Sponsors and Exhibitors

    Official Media Partner

    Supporters

    ATTENDEES 2019

    Download

    Interview with Michael Becker, Boehringer Ingelheim Pharma GmbH & Co. KG

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    Interview with Shannon E. Clark, CEO, UserWise

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    Interview with Mathieu Rigollet, Roche

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    Interview with Joan Malmstrøm, Principal Scientist, Novo Nordisk

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    Interview with James Mellman, Device Manager, Novartis

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    Attendees 2017-18

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    Interview with Alexander Zuern, Device Testing Manager, Novartis

    Download

    Workshop B

    Download

    Workshop A

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    Speaker Line-up

    Download

    Conference Programme

    Download

    Presentation by Steve Chamberlain, GSK

    Download

    Presentation by Takuya Minezaki, Mitsubishi Gas Chemical

    Download

    Presentation by Vikas Jaitely, Merck

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    Presentation by Marcel Muller, Novartis

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    Presentation by M. Hemminger PTDE-D, Roche

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    Presentation by Liz Baker, MHRA

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    Chair Letter

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    Pre-Filled Syringes & Injectable Drug Devices Infographics

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    Sponsors and Exhibitors


    EVEON

    Sponsors and Exhibitors
    http://www.eveon.eu

    Transforming patient experience. EVEON is the partner of pharmaceutical, biotech companies and medical device manufacturers for the development of automatic, safe and connected devices. The company facilitates and controls the handling, preparation and administration of molecules. Our innovative solutions meet specific requirements of a wide range of applications.


    Harro Höfliger

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

    Harro Höfliger specializes in the development of customer-oriented process and production solutions for pharmaceutical and medical applications as well as market-oriented consumer products. In addition to innovative machine platforms and packaging machines, customized turnkey system solutions for product assembly, processing of web materials, as well as dosing and inhalation technology are the company’s core expertise.

    The systematically structured portfolio of upscalable test machines and modules, as well as requirement-oriented technology platforms, results from many years of experience and targeted research and development. Thus, Harro Höfliger covers all phases from the laboratory stage to high-performance production.



    Mikron

    Sponsors and Exhibitors
    http://www.mikron.com/automation

    Mikron Automation is your partner for scalable and customized assembly systems – from the first idea to the highest performance solutions. The Automation division has 620 employees dedicated to design and build your solutions at its 5 sites and support you wherever you are in the world.


    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.


    Nelson Labs Europe

    Sponsors and Exhibitors
    http://www.nelsonlabs.be

    Nelson Labs Europe is an independent contract research organization, specializing in and fully dedicated to providing premium Extractables & Leachables services to the pharmaceutical industry. Based in Belgium, Nelson Labs Europe supports pharmaceutical companies – across the globe in developing worldwide compliance testing strategies to qualify Container/Closure Applications and Pharmaceutical Production Equipment from an Extractables & Leachables perspective. Over the last 15 years, Nelson Labs Europe supported over 200 submissions to the FDA and to the EMA.

    From a quality perspective, Nelson Labs Europe is ISO 17025 accredited and GLP-certified. Nelson Labs Europe has received a GMP accreditation from the European Authorities.

    Nelson Labs Europe is FDA registered. In 2017, Nelson Labs Europe was successfully audited by the FDA.

    Nelson Labs Europe is part of Nelson Labs, the leading global micro-biological and analytical lab testing platform.

    Nelson Labs, along with sister companies Sterigenics and Nordion, are part of Sotera Health, the world’s leading, fully-integrated protector of global health.



    Nemera

    Sponsors and Exhibitors
    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.


    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.


    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.


    PHC Corporation

    Sponsors and Exhibitors
    http://www.phchd.com/global

    In April 2018, Panasonic Healthcare Holdings Co., Ltd. changed its name to PHC Corporation.

    For all the people who wish for better health. Over the approximately 70 years since our establishment, we have delivered groundbreaking products to the world. The newly created “PHC” will take on the challenge of providing ever new innovations, drawing on the spirit of monozukuri (Japanese manufacturing).We will continue to evolve as a provider of devices and services marked by PHC's precision technology in our three core business areas of Medical Devices, Healthcare IT, and Life Sciences.



    Schott AG Pharmaceutical Systems

    Sponsors and Exhibitors
    http://www.schott.com/uk/english/index.html

    SCHOTT is a leading international technology group in the areas of specialty glass and glass-ceramics. With more than 130 years of outstanding development, materials and technology expertise we offer a broad portfolio of high-quality products and intelligent solutions that contribute to our customers’ success. SCHOTT Pharmaceutical Systems is one of the world’s leading suppliers of primary packaging and specialized analytical lab services for the pharmaceutical industry. We provide our customers quality solutions while meeting their highest demands with our expertise and broad product portfolio; including ampoules, cartridges, vials and syringes made of glass and COC polymer. Our state-of-the-art production facilities and our products comply with the highest international quality standards for pharmaceutical needs.


    ZEON Europe GmbH

    Sponsors and Exhibitors
    http://www.zeon.eu/cop-copf-zeonex-zeonor-zeonorfilm.html

    Zeon Europe GmbH is the European marketing/sales organisation of Zeon Corporation / Japan. As part of specialty materials operations Zeon produces Cyclo-Olefin Polymers (COP) under the tradenames ZEONEX® and ZEONOR®. The balance of outstanding water barrier properties in combination with high purity, excellent chemical resistance, high transparency and low interaction with drugs, put ZEONEX® and ZEONOR® as a perfect alternative to glass or other plastics solutions for pharmaceutical and biopharmaceutical containers - such as Pre-filled syringes, cartridges and vials.


    ZwickRoell

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

    ZwickRoell manufactures and supports a wide range of materials testing machines, systems and accessories for use in research, quality control, production environments and academia. Our extensive portfolio of testing machines and accessories cover almost every segment, from medical and pharmaceutical packaging to surgical instruments and orthopaedics and biomaterials.

    Media Partners


    Pharma Journalist

    Official Media Partner
    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.


    Samedan

    Official Media Partner
    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.


    Drug Discovery Today

    Official Media Partner
    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.


    Drug Development & Delivery

    Official Media Partner
    http://www.drug-dev.com

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


    World Pharma News

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



    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.

    Media Partners


    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.


    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….


    SciDoc Publishers

    Supporters
    http://www.scidoc.org

    SciDoc Publishers is a major source provider of e-journals in the field of Science, Technology and Medicine (STM). The nature of journals - Open Access and Peer-reviewed. We are aimed with a sole motive in making a mark in the field of Open Access, by propagating the knowledge to the scientific community. Our prime concern involves, the knowledge to reach millions of readers and give them access to scientific publications - online.


    GBI

    Supporters
    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.


    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.


    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.


    European Biotechnology Network

    Supporters
    http://european-biotechnology.net/

    The European Biotechnology Network is dedicated to facilitating co-operation between professionals in biotechnology and the life sciences all over Europe. The non-profit organisation brings research groups, universities, SMEs, large companies and indeed all actors in biotechnology together to build and deliver partnerships.


    PharmaVOICE

    Supporters
    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.


    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.


    Select Science

    Supporters
    http://www.selectscience.net/

    SelectScience is an independent, online information resource for the worldwide scientific community, and the home of trusted information for laboratory scientists. Discover impartial, expert opinion and trusted reviews about latest laboratory equipment and techniques; plus videos, application notes and science news from around the world. Become a member for free today.


    pharmaphorum

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    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


    pharmanews hq

    Supporters
    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.


    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


    Gate2Biotech

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    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.


    Biocompare

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    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.


    Farmavita

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    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!


    Drug Development Technology

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    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.

    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
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