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Injectable Drug Delivery

The SAE Media Group is pleased to announce the second annual Injectable Drug Delivery conference which will be held in London on the 15th and 16th May 2019.

The global injectable drug delivery market is expected to grow from $400 billion to $1200 billion by 2046 with a CAGR of 12.8%.

Injectable drug delivery is a method of drug administration into the body with a needle via various routes including intramuscular and intravenous. These are examples of conventional drug delivery. Recently, there has been a focus on novel drug delivery, including needle-free injectors, and transdermal patches. Long acting injectables (LAI) are developing fast as a push towards patient centric devices drives the industry. Habitually, injectables were used for delivery of hormones, vaccines and insulin but as technology advances the application is continuing to expand. Now there is an emphasis on finding solutions to chronic conditions and the biological drugs required involve formulation development challenges for proteins, including high viscosity and high volume. Self-administrative, connected, and ergonomic devices are the new drive. Self-injectable devices include pen injectors for diabetic patients. The wealth of expansion available in the field of connected devices is huge. The regulatory landscape is challenging as it evolves rapidly with the market demand for new devices.
 

FEATURED SPEAKERS

Adeline Meilhoc

Adeline Meilhoc

VP Sales & Marketing, Eveon
Edward Sims

Edward Sims

Senior Designer & Associate , Crux Product Design, Ltd
Joel Richard

Joel Richard

Head of Technical & Pharmaceutical Operations, MedinCell
Louisa Harvey

Louisa Harvey

Director, Harvey Medical Consulting Ltd
Paula Wood

Paula Wood

Director, Human Factors Centre Ltd
Quentin Le Masne

Quentin Le Masne

Head of Engineering team - Electro-Medical, Drug Delivery Devices, Merck
Stephen Paboojian

Stephen Paboojian

Senior New Technology Project Leader II, Novartis Pharma AG
Vasco Filipe

Vasco Filipe

Senior research scientist - Formulation Development, Sanofi

Adeline Meilhoc

VP Sales & Marketing, Eveon
Adeline Meilhoc

Adeline Meilhoc is an expert in drug clinical development and in digital environment around medical devices. She is specialist of innovation product setup and deployment dedicated to patients and health care professionals. In the last 15 years, she proposes commercial and operational partnership solutions to pharma and biotech industry. She accompanies them in their efforts to enhance patient's treatment adherence in analyzing health real-world data. Clinical psychologist, specialist in Health & Society, she is focusing now on international commercial deals for drug preparation and administration, in proposing a bridge between R&D and Market access.

Edward Sims

Senior Designer & Associate , Crux Product Design, Ltd
Edward Sims

Edward is an established designer with a wealth of expertise in usability testing and human factors. In his role as Senior Designer & Associate at Crux, Edward works at the forefront of R&D across the medical and consumer goods sectors and promotes a user-centred approach to design better products faster. Edward has significant experience in the development and usability testing of injectable, inhalation, ocular and connected drug delivery devices, and has developed instructions for use (IFUs) for injection systems on the market. Prior to joining Crux Edward helped bring several flagship products to market for British technology company Dyson.

Ian Culverhouse

Director, Rebus Medical Ltd
Ian Culverhouse

Dr Ian Culverhouse is Co-Founder of Rebus Medical Ltd and an experienced human factors consultant, having worked with companies which include Roche, AstraZeneca, Eli Lilly, Smith and Nephew and Bosch Healthcare. Ian has a wealth of experience in applying HFE to the design of medical devices including pre-filled syringes, auto-injectors, large volume injectors, patch pumps and closed loop insulin infusion systems. Ian advocates integrating HFE from the outset of a development programme and has a PhD related to applying early stage prototyping techniques to maximise user input and concept evaluation into the design process.

Joel Richard

Head of Technical & Pharmaceutical Operations, MedinCell
Joel Richard

Dr Richard is presently leading the Technical and Pharmaceutical Development activities for the Medincell Company, Lead Candidate Selection to all Clinical Development Phases.
 

Dr Joël Richard graduated from Ecole Normale Supérieure (Cachan, France) and got his PhD in Materials Science/Colloids & Interface Science from University of Paris VI. Dr Richard has 30 years of experience in chemistry and biopharmaceutical R&D, including several global senior leadership positions in various Biotech and Pharma companies, such as Medincell, Ipsen, Merck Serono, Serono and Ethypharm. He also had an entrepreneurial experience, co-funding Mainelab (France) with Pr Jean-Pierre Benoit, a drug delivery company specialized in developing solvent-free processes for protein delivery systems. Dr Richard has focused his research activity on new formulations and drug delivery systems (such as microspheres, nanoparticles, self-assembling gel systems, chemically-modified proteins, supercritical fluid technology . . .), especially for injectable protein and peptide formulations. Dr Richard has published 68 peer-reviewed scientific papers, 8 book chapters and 2 editorials in various fields (colloids and interfaces, drug delivery, supercritical fluids, protein formulations, sustained-release formulations…). He is the author of more than 140 international communications and 55 patent families.

 

John Burke

Senior Consultant, Team Medical Devices
John Burke

John specializes in the design and project management of medical devices with a particular focus on the development of parenteral drug delivery devices. A designer by training with a strong grounding in medical design and regulatory focused human factors, he regularly attends user studies in both Europe and the US.
 

On projects he seeks to balance technical, user and commercial requirements to produce simple elegant solutions. Over the years, John has worked on a range of parenteral device developments with leading pharma companies in both Europe and the US and has a good knowledge and understanding of the market, current devices and trends.
 

John brings experience of both consumer and medical product development, having worked on a diverse range of products, including drug delivery devices, wound management, diagnostics platforms and blood glucose monitoring.
 

Louisa Harvey

Director, Harvey Medical Consulting Ltd
Louisa Harvey

Louisa is an experienced medical device human factors consultant. Louisa has an MSc in Industrial Pharmaceutical Science and began her career working in clinical trials. Louisa has a broad-range of experience working in both the pharmaceutical and medical device industries in technical and commercial roles. Having spent a number of years working with most of the Cambridge-based medical consultancies, she has inputted into the design of many different products from auto-injectors through to large surgical systems.

Louisa specializes in conducting studies in vulnerable patient groups always ensuring her studies are designed with ethics in mind from the outset.
 

Mark Hassett

Vice President of Business Development, Credence MedSystems, Inc.
Mark Hassett

Mr. Hassett has 30+ years’ experience in the medical device industry. In that time, he has functioned as Global VP Sales, Marketing, and Business Development for IVAC Corporation, Medication Delivery Devices, Safety Syringes Inc., ROVI Contract Manufacturing and other innovative delivery system companies. His responsibilities included commercialization of infusion pumps, injectable devices with prefilled syringes, wearable devices, and autoinjectors. He has injectable device experience in multiple markets including acute and home care as well as 15 years of experience specifically in Pharmaceutical and Biotech space. He holds a BS degree from Georgia State University in Atlanta, GA.
 

Mayur Patel

Medical device expert – Managing consultant, PA Consulting
Mayur Patel

Mayur Patel is an experienced Project Manager and Clinical Scientist [Health and Care Professions Council UK registered CS18187 – a regulated professional qualification required to advise safety and effectiveness of medical devices/ physiological measurement techniques in the NHS]. He has a strong track record in leading the development of innovative devices and techniques in medical and drug-device combination device sectors. Mayur holds a Masters Degree in Engineering and Physical Science in Medicine from Imperial College London. He lectures King’s College London postgraduate students and trainee clinical scientists on a range of medical device and healthcare management subjects.

Miranda Newbery

Director, Inspired Usability
Miranda Newbery

Miranda is a creative design and usability consultant specialising in medical device developments. In 2016 she founded Inspired Usability, a medical device human factors consultancy. She works on early design research through to human factors validation on a range of medical device and combination products. Miranda originally studied Engineering (Cambridge University) and Industrial Design (Royal College of Art) and is a chartered ergonomist with the CIEHF. In 2018 Miranda and Louisa Harvey started the Medical Human Factors Network UK, with the aim of brining together like-minded professionals and raising the bar with medical human factors practitioners.

Paula Labat-Rochecouste

Director of Human Factors, Human Factors Centre Ltd
Paula Labat-Rochecouste

Paula has a background in Human Factors, Usability, User Experience (UX/UI) and Product Design. Paula specializes in Medical Device Design and Consumer Health. Her expertise spans across front end user research through to formative (verification) and summative (validation) testing. Paula is an experienced Moderator and has conducted studies across Europe, USA and China. She has a passion for identifying unmet needs and ensuring effective user input is integrated into the entire product development process.

Paula Wood

Director, Human Factors Centre Ltd
Paula Wood

Paula has a background in Human Factors, Usability, User Research, User Experience and Product Design. Paula specialises in both Medical Device Human Factors and Human Factors for Combination Products. She is a certified Practitioner and has moderated numerous Formative and Summative Evaluations across Europe, USA and China. Paula is also a licentiate fellow of the Institute of Training and Occupational Learning and provides Human Factor’s training to both Pharmaceutical and Medical Device manufacturers.

Quentin Le Masne

Head of Engineering team - Electro-Medical, Drug Delivery Devices, Merck
Quentin Le Masne

Quentin Le Masne holds a Master’s Degree in Engineering for Ecole Centrale de Paris and a PhD in Physics from Paris University. He has worked in numerous positions in the field of medical devices, from In-Vitro Diagnostic to Drug Delivery Devices, restlessly bringing highly innovative ideas from lab to market. His work focuses on the management of engineering teams with diverse expertise like electronic, mechanics, human factors, physics, fluidics, and manufacturing to bring new products in the doctor’s and patient’s hands. He is now in charge of the development of novel electronic drug delivery devices for Merck.

Sigrid Van Dyck

Senior Director Technical Operations, Janssen Supply Chain, Johnson & Johnson
Sigrid Van Dyck

Sigrid Van Dyck is a Senior Director at Johnson & Johnson, located in Switzerland, where she leads the Technical Operations Parenteral Technology Platform. She is managing New Product introduction and Life Cycle Management of biological and other parenteral products, as well as providing technical support to the internal and external network.

Sigrid joined J&J in 2006 as a Senior Scientist, supporting various New Product Introductions. Her professional career started with Schering-Plough Belgium, where she held positions in Quality and Sterile Manufacturing Operations. Sigrid holds a Ph.D. in Pharmaceutical Sciences.
 

Stephen Paboojian

Senior New Technology Project Leader II, Novartis Pharma AG
Stephen Paboojian

Stephen Paboojian is an engineer and senior project leader for the development of pharmaceutical delivery systems, from medical devices and primary drug packaging to instructional materials and custom outer packaging. Steve has a proven track record of over 25 years of driving novel inventions from concept to commercial launch, contributing to global products in development for treatment of Macular Degeneration, COPD, Cystic Fibrosis, Multiple Sclerosis, and Diabetes.

Tom Lawrie-Fussey

Head of Digital Health, Cambridge Design Partnership
Tom Lawrie-Fussey

Tom Lawrie-Fussey is a digital services specialist at technology and product design firm Cambridge Design Partnership. He is a Chartered Engineer with a master’s degree and has more than 15 years’ product development experience. Tom works across multiple industry sectors, primarily focused on drug delivery, consumer health, and FMCG clients, where he drives various digital initiatives to help guide clients along their own digital roadmap. He specialises in digital implementation, linking device development with communications and data analytics platforms. Tom provides a technology-agnostic, pragmatic approach that is human-centred – unlocking benefits for all stakeholders and, ultimately, generating new revenue streams.

Vasco Filipe

Senior research scientist - Formulation Development, Sanofi
Vasco Filipe

Vasco Filipe is a Biological Engineer and obtained a Ph.D. degree in Pharmaceutical Sciences from the Utrecht University (The Netherlands) in 2011. His thesis focused on the physicochemical characteristics, stability in biological fluids and immunogenicity of monoclonal antibody aggregates. After a post-doc in 2012 on a similar topic, he then joined Adocia in 2013 (Lyon, France), where he worked as the Project Leader for all monoclonal antibodies collaborations. In 2015 he joined Sanofi (Paris, France), where he now works as a Section Head of Formulation and Process Development in the department of Biologics Drug Product Development.

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

Joel Richard, Head of Technical & Pharmaceutical Operations, MedinCell

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9:10

Overcoming the challenges in development of injectable protein formulations

Vasco Filipe, Senior research scientist - Formulation Development, Sanofi

  • High viscosity that exceeds the capabilities of current manufacturing practices or available parenteral delivery methods
  • High concentration leading to stability and aggregation concerns and the associated material required for a robust development strategy
  • High volume biologic challenges and strategies to overcome them
  • Viscosity reducing excipients
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    9:50

    Injectable Drugs – from hospital to home care, a need for transforming patient and health care professional experience

    Adeline Meilhoc, VP Sales & Marketing, Eveon

  • Thinking real-world data collection: the added-value of digital enhancement to serve patient treatment compliance and HCP security
  • How injectable drug delivery could be optimized within hospital block chain
  • Human Factor Engineering: where smart injectable drug delivery is saving lives in emergency scenarios
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    10:30

    Morning Coffee

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    11:00

    Formulation development for long acting injectables

    Joel Richard, Head of Technical & Pharmaceutical Operations, MedinCell

  • Considerations for long-acting formulation development
  • Overcoming challenges
  • A game-changing delivery system for long acting injectables
  • Future prospects
     
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    11:40

    Development of Visisure, a novel low volume high accuracy syringe for delivery of Lucentis to neonates

    Stephen Paboojian, Senior New Technology Project Leader II, Novartis Pharma AG

  • Background on Retinopathy of Prematurity and impact to patients
  • Drivers and constraints for development: user, business, and regulatory
  • Technical challenges overcome: device, packaging, manufacturing, and HFE
  • Final product configuration and supply chain 

  •  

     

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    12:20

    Networking Lunch

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    13:20

    Ethical principles in human factors studies and developing a code of conduct

  • Overview of current HF study trends
  • Ethical considerations of HF Studies
  • Proposed considerations for ethical code of conduct

     

  • Miranda Newbery, Director, Inspired Usability

    Louisa Harvey, Director, Harvey Medical Consulting Ltd

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    14:00

    Sprint: How to quickly answer key usability questions and create patient-centric devices.

    Edward Sims, Senior Designer & Associate , Crux Product Design, Ltd

  • Overview of the Design Sprint process
  •  Using Sprints to create patient-centric devices
  • How to integrate Sprints with human factors and usability engineering activities
  • Opportunities for the business and patients 
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    14:40

    Afternoon Tea

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    15:10

    An approach to linking Human Factors findings through Design Control

  • Illustration of methods to track use related risks through design and development that links to users needs
  • Foreseeable use related issues associated with the usability engineering process
  • User interface requirements through the design and development process
  • Paula Labat-Rochecouste, Director of Human Factors, Human Factors Centre Ltd

    Ian Culverhouse, Director, Rebus Medical Ltd

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    15:50

    Chairman’s Closing Remarks and Close of Day One

    Joel Richard, Head of Technical & Pharmaceutical Operations, MedinCell

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Sigrid Van Dyck, Senior Director Technical Operations, Janssen Supply Chain, Johnson & Johnson

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    9:10

    Driving innovation in the drug delivery market

    Mayur Patel, Medical device expert – Managing consultant, PA Consulting

  • Future of the drug delivery market - an overview 
  • How we can improve patient adherence with connectivity and innovation
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    9:50

    Development of electronic auto-injectors - from concept to manufacture

    Quentin Le Masne, Head of Engineering team - Electro-Medical, Drug Delivery Devices, Merck

  • Overview of the development process – the do’s and don’ts
  • The challenges and learnings of electronic and connected drug delivery devices
  • User experience and patient-centric design: what do patients really want from electronic auto-injectors?
     
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    10:30

    Morning Coffee

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    11:00

    Digital rapid prototyping-using the latest prototyping methods to unlock the value of digital propositions faster

    Tom Lawrie-Fussey, Head of Digital Health, Cambridge Design Partnership

  • Case studies that navigate through the risks and rewards of deploying digital into healthcare products and services
  • Learn how we uncover surprising insights in human factors and product development
  • We’ll share a number of toolkits and approaches we use which help us to better quantify user experiences; highlighting where the value in digital can be captured and monetised.
     
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    11:40

    Innovative device solutions in response to specific market needs

    Mark Hassett, Vice President of Business Development, Credence MedSystems, Inc.

  • Introduction to Credence MedSystems: a developer of innovative injection devices
  • Plans to continue to expand device platforms with customized injection systems
  • Overview of the importance of supporting the growth of specific therapeutic applications
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    12:20

    Networking Lunch

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    13:20

    Partners in evolution: Challenges and changes in parental drug delivery

    John Burke, Senior Consultant, Team Medical Devices

  • A summary of key trends and changes in the device landscape
  • Highlight potential pitfalls to avoid
  • The device as an enabler rather than a barrier to market success
     
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    14:00

    Manufacturing, filling and quality control

    Sigrid Van Dyck, Senior Director Technical Operations, Janssen Supply Chain, Johnson & Johnson

  • Device Design - long acting injectables and biologics
  • Design for manufacturing - filling, automated inspection and packaging
  • Quality assurance considerations
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    14:40

    Afternoon Tea

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    15:10

    Manufacturing inspection trends

    • History, standards & regulatory expectations
    • Manual Inspection
    • Automated Inspection
    • Future trends
     

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    15:50

    Chairman’s Closing Remarks and Close of Day Two

    Sigrid Van Dyck, Senior Director Technical Operations, Janssen Supply Chain, Johnson & Johnson


    VP Sales & Marketing
    Eveon
    Senior Designer & Associate
    Crux Product Design, Ltd
    Director
    Rebus Medical Ltd
    Head of Technical & Pharmaceutical Operations
    MedinCell
    Senior Consultant
    Team Medical Devices
    Director
    Harvey Medical Consulting Ltd
    Vice President of Business Development
    Credence MedSystems, Inc.
    Medical device expert – Managing consultant
    PA Consulting
    Director
    Inspired Usability
    Director of Human Factors
    Human Factors Centre Ltd
    Director
    Human Factors Centre Ltd
    Head of Engineering team - Electro-Medical, Drug Delivery Devices
    Merck
    Senior Director Technical Operations
    Janssen Supply Chain, Johnson & Johnson
    Senior New Technology Project Leader II
    Novartis Pharma AG
    Head of Digital Health
    Cambridge Design Partnership
    Senior research scientist - Formulation Development
    Sanofi

    Sponsors and Exhibitors

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    Preliminary Attendees 2019

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    An interview with Sigrid Van Dyck, Johnson & Johnson

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    An interview with JOËL RICHARD, MedinCell

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    An interview with QUENTIN LE MASNE, Merck

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    An interview with VASCO FILIPE, Sanofi

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    Invitation from the Chair 2019

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    Speaker line-up

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    Past Attendees 2018

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    Conference Programme 2019

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    Presentation by Uri Baruch, Cambridge Design Partnership

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    Presentation by Pierre Goldbach, Roche

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    Presentation by Michhael Hooven, Enable Injections

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    Presentation by Jayne Lawrence, The University of Manchester

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    Presentation by Francesco Malavasi, Novartis

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    Presentation by Fie Falck Larsen, Leo

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    Presentation by Cedric Gysel, Johnson & Johnson

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    Presentation by Andrew Fiorini, GSK

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    Presentation by Dr. Ahmed Youssef, Sanofi

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    Sponsors and Exhibitors


    Almac

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

    Almac is an established CDMO organization that provides an extensive range of integrated services to the global biopharma industry. Almac provides specialised packaging solutions for all biopharmaceutical dosage forms (vials, ampoules, pre-filled syringes, auto-injector pens) and can support all your packaging needs from niche/orphan drug launches to high volume products.


    Crux Product Design Ltd

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

    Crux is a product development consultancy serving the pharmaceutical industry with a fully integrated service wrapped around solid technical knowledge. Our highly experienced team consists of industrial designers, mechanical engineers, electronics & software engineers and simulation experts. We’re trusted by our clients to solve their most technically challenging briefs.


    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.

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    Mednous

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    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


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    Gate2Biotech

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


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    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!


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    ONdrugDelivery Magazine

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


    Pharmalicensing

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    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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    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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