Our latest COVID-19 information - full Autumn programme of webinars now in place

Medical Devices Faculty

The following expert presenters are scheduled to present our courses:

Tina Amini

Dr. Tina Amini, a pharmacist with PhD in Pharmaceutics, is Director of Medical Device Division at NDA Group. She has over 30 years experience in Pharmaceutical and Medical Devices. She previously...

Speaking on Drug/Device and Device/Drug Combinations in the EU and USA
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Stuart Angell

Stuart Angell is a joint director in his own consultancy specialising in global regulatory affairs strategy and compliance for in vitro diagnostics and medical devices focusing on the transition...

Speaking on Introduction to the In-Vitro Diagnostic Regulation (IVDR)
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Speaking on Injectable Drug Delivery
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Elizabeth Baker

Elizabeth is Group Manager, Licensing Group 1 and Drug/Device Enquiries, MHRA. The unit has responsibility for advising on the drug/device borderline, advising on regulatory aspects of drug/device...

Speaking on Drug/Device and Device/Drug Combinations in the EU and USA
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Speaking on The Medical Device Summer School - From Concept to CE Marking
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George Barrie

George Barrie is a Consultant to the Pharmaceutical Packaging Industry.
Until recently he was with Actavis where his role was to bring all elements of packaging design, regulatory requirements and...

Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
Full details...

Janette Benaddi

Janette Benaddi is a business mentor, international speaker/trainer and consultant to the medical device industry. Janette has over 25 years’ experience of managing pre and post market clinical...

Speaking on EC Medical Devices Vigilance System and Post Marketing Surveillance
and 8 more Full details...

Speaking on Nasal Drug Delivery
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Gregory Berman

Gregory is Head of the Medical Group at Kinneir Dufort, an award-winning research, innovation, design and product development company, with over 30 years’ experience helping companies discover,...

Speaking on Injectable Drug Delivery
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Rene Bommer

Dr. René Bommer is a founder and an owner of pharmAccel Consulting.
He received his Ph.D. in Chemistry from the University of Constance in Germany in 1990. After research positions at the Scripps...

Speaking on Nasal Drug Delivery
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Speaking on Cyber Security for Medical Devices
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Laura Brown

Dr Laura Brown MBA, BSc (Biochemistry), BSc (Psychology), PhD, Diploma in Clinical Science, FICR, is a Pharmaceutical Management and Training Consultant, Course Director for the MSc in Clinical...

Speaking on Managing Vendor/CRO/CMO Oversight
and 3 more Full details...

Will Burton

Will Burton, Director of Russell Square Quality Representatives (RSQR) Ltd, is engaged in providing a range of consultancy and training services to the international medical device, pharmaceutical...

Speaking on An Introduction to the Medical Device Regulation
and 2 more Full details...

Grant Castle

Grant Castle is a Partner in the London office of Covington & Burling, practicing in food and drug regulatory law, with an emphasis on pharmaceutical and medical device regulation and associated...

Speaking on EC Medical Devices Vigilance System and Post Marketing Surveillance
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Dale Charlton

Dale Charlton is a Freelance Consultant for automation and fill / finish. Dale has spent a lifelong career in Life Sciences and Biotechnology encompassing both the academic and industrial...

Speaking on Pre-Filled Syringes: End-to-End Processing
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Speaking on The Medical Device Summer School - From Concept to CE Marking
Full details...

Philip Clay

Philip Clay is Director and principal toxicologist with Chorley Consulting. He is a UK and European registered toxicologist and specialises in product safety assessment with over 30 years’...

Speaking on Biological Evaluation of Medical Devices
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Koen Cobbaert

Koen Cobbaert is Quality and Regulatory Manager at Philips Healthcare. He represents COCIR in numerous work groups at European level. Koen has over 15 years of hands-on experience in establishing...

Speaking on The Medical Device Summer School - From Concept to CE Marking
and 1 more Full details...

Nancy Consterdine

Nancy Consterdine is a joint director in her own consultancy specialising in global regulatory affairs strategy and compliance for in vitro diagnostics and medical devices, focusing on the...

Speaking on Introduction to the In-Vitro Diagnostic Regulation (IVDR)
Full details...

Bruce Davis

Bruce Davis runs his own training/consultancy company for science and risk based approaches to Engineering and Process Validation (PV), Quality by Design (QbD), Quality Risk Management, GMP for...

Speaking on Effective Technology Transfer
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Speaking on Nasal Drug Delivery
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Richard Featherstone

Richard Featherstone is Research Director, Human Factors Research & Design, Emergo by UL, and previously Managing Director of Medical Device Usability Limited, a specialist human factors...

Speaking on Nasal Drug Delivery
and 1 more Full details...

Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
Full details...

Ben Forbes

Ben Forbes is a Professor of Pharmaceutics at King’s College London. He is currently the Head of the Pharmaceutics Teaching Section and the Drug Delivery Research Group of the Pharmaceutical...

Speaking on Nasal Drug Delivery
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Speaking on Nasal Drug Delivery
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Speaking on Nasal Drug Delivery
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Barbara Grossman

Barbara is a Biochemist and a Medical Writer, Editor and Teacher by profession, with 20+ years’ experience in the pharmaceutical industry. Barbara has started her own medical writing and...

Speaking on Effective Technical Writing & Editing
and 1 more Full details...

Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
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Speaking on Medical Device Regulation in the Eurasian Union, Russia and the CIS
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Heba Hashem

Heba has been working with Regulatory Affairs in the Middle East for more than 25 years. She has a Pharmaceutical and Business background being a graduate of the Faculty of Pharmacy (Cairo...

Speaking on Medical Device Regulations in the Middle East and North Africa
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Mike Holroyd

Mike Holroyd is Senior Director with responsibility for the design, development and scale-up of inhalation devices within the Mylan Global Respiratory Group. He has an MA in Engineering from St....

Speaking on Dry Powder Inhalers
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David Howlett

In 2003 David established PharmaDelivery Solutions Ltd as a specialised consultancy service in the field of drug delivery combination products (especially respiratory) device technology. This has...

Speaking on Dry Powder Inhalers
and 2 more Full details...

Jonathan Hughes

Jonathan Hughes, Ph.D., FTOPRA, has over 32 years of worldwide regulatory and clinical affairs experience across medical devices, drug / biologic – device combination products and in-vitro...

Speaking on FDA Approval Process for Medical Devices
Full details...

Janine Ingleby

Janine Ingleby is a Senior Safety Assessor with Chorley Consulting. She holds a MSc in Global aquatic biodiversity and a BSc in Molecular biology and biotechnology, both from the University of...

Speaking on Biological Evaluation of Medical Devices
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Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
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Theresa Jeary

Theresa Jeary holds a Master’s Degree in Pharmaceutical Science and is eligible to be a Pharmaceutical Qualified Person.

Theresa has over 25 years’ experience working in both the...

Speaking on An Introduction to the Medical Device Regulation
and 2 more Full details...

David Jefferys

Dr David Jefferys is Senior Vice President for Global Regulatory, Government Relations, Public Affairs and Patient Safety (EMEA, Russia and Australasia) at Eisai. After qualifying, he worked in...

Speaking on Drug/Device and Device/Drug Combinations in the EU and USA
and 1 more Full details...

Speaking on The Medical Device Summer School - From Concept to CE Marking
Full details...

Horst Koller

Horst Koller started his professional career in 1994 to work for a large pharmaceutical company in Germany managing the Process Engineering Group. He holds a degree as Dipl. Ing (FH) in...

Speaking on Pre-Filled Syringes: End-to-End Processing
Full details...

Zuzanna Kwade

Zuzanna Kwade is Medical Affairs Manager, Agfa Healthcare. Zusanna holds a PhD in Biochemistry and has more than ten years of experience in clinical and medical research. She is the co-author of...

Speaking on Medical Device Software: Complying with the MDR & FDA Regulations
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Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
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Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
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Speaking on Injectable Drug Delivery
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Helen Muirhead

Helen Muirhead is now an independent Respiratory Medicine Expert, acting as a consultant after 30 years with GSK in both R&D and Manufacturing. Helen is also involved in teaching at Universities...

Speaking on Dry Powder Inhalers
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Speaking on Nasal Drug Delivery
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Chris Penfold

Chris Penfold is an experienced Freelance Packaging Development Specialist and Consultant.

Chris Penfold is a self-motivated, achievement orientated, confidant and creative leader with a proven...

Speaking on An Introduction to Pharmaceutical Packaging
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Speaking on Injectable Drug Delivery
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Ilona Putz

Ilona Putz founded PULONA Emerging Markets based in the UAE which is dedicated to creating and developing tailor-made business concepts for clients in the healthcare sector across the Middle East....

Speaking on Medical Device Regulations in the Middle East and North Africa
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Speaking on Nasal Drug Delivery
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Andreas Rothmund

Dr. Andreas Rothmund is Qualified Person at Vetter Pharma-Fertigung in Ravensburg, Germany, an independent contract manufacturer specialised in the aseptic production of pre-filled application...

Speaking on Pre-Filled Syringes: End-to-End Processing
Full details...

Regina Scherließ

Prof. Dr. Regina Scherließ (*1979) is a professor for Pharmaceutics and Biopharmaceutics, director of the section Pharmacy and chair of the Department of Pharmaceutics at Kiel University,...

Speaking on Nasal Drug Delivery
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Speaking on The Medical Device Summer School - From Concept to CE Marking
Full details...

Speaking on Nasal Drug Delivery
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Paul Sim

Paul Sim, Regulatory Affairs Manager, BSi Group. Paul has worked in the healthcare industry for 34 years and is currently Project Managing BSI’s implementation of EU Commission Recommendation...

Speaking on Technical Documentation to Comply with the MDR and IVDR
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Speaking on Nasal Drug Delivery
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Speaking on Medical Device Studies: Clinical Evidence
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Speaking on EC Medical Devices Vigilance System and Post Marketing Surveillance
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Julie Suman

Dr. Julie D. Suman, R.Ph., Ph.D., is a co-founder and President of Next Breath, LLC, an incubator company located at the UMBC Technology Center. Next Breath, which incorporated in April 2002, is a...

Speaking on Nasal Drug Delivery
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Greg Thay

Greg Thay is the founder and principle human factors consultant at THAY Medical, and has over twenty years’ experience in the medical and pharmaceutical industries. He has worked in many therapy...

Speaking on The Medical Device Summer School - From Concept to CE Marking
Full details...

Speaking on Pre-Filled Syringes: End-to-End Processing
Full details...

Speaking on Injectable Drug Delivery
Full details...

Speaking on Nasal Drug Delivery
Full details...

Speaking on Pharmaceutical Packaging, Labelling and Artwork Origination
Full details...

Speaking on Injectable Drug Delivery
Full details...

Andrew Willis

Andrew Willis is an independent consultant providing expert advice and training on global regulatory solutions and pharmaceutical development. Previously, he worked for Catalent Pharma Solutions...

Speaking on Development of Combination Products: Critical Interactions
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Alison Wilson

Alison is an Independent Regulatory Affairs Consultant. Previously Regulatory Affairs Manager for Smith & Nephew Wound Management, she has over 25 years’ experience of regulatory affairs in...

Speaking on Drug/Device and Device/Drug Combinations in the EU and USA
and 1 more Full details...

Speaking on Injectable Drug Delivery
Full details...