Medical device course owners

Our course owners are experts in their fields. Together, they have decades of industry and specialist subject experience having implemented the standards themselves. They know and understand the challenges you’re most likely to face, so can suggest the best and most effective ways to help you overcome them. Many of them have also trained the assessors who check your organization’s compliance to standards.

Come on one of our courses and you can be confident of our course owners’ training skills. Not only do they develop and continually refine the courses, which means they know the material inside out, but they also use accelerated learning techniques. They understand that each of us learns in different ways whether it’s visual, practical or through interaction so they structure the courses around you. It’s one of the reasons why our courses have outstanding pass rates and why 99% of our course delegates would recommend us.

To help turn your business into a truly excellent one, your course owner won’t just share their knowledge with you; they’ll also show you the right way to use that knowledge. Turn their experience into your expertise.

Course owners

Each BSI medical device course is owned by an expert in that field to ensure that we keep material cutting edge, with over 60 expert trainers worldwide, please contact your local BSI for details of courses. Learn more about our expert course owners and their experience, qualifications and specialist subject areas.

Amie Smirthwaite - Clinical Evaluation, Post Market Surveillance and Vigilance, Introduction to CE Marking, ISO 14971 Risk Management

Aneela Lala - ISO 14971 Risk Management, Post Market Surveillance and Vigilance, Process Validation and Technical Writing

Ann Goodall - ISO 13485, CE marking for In-Vitro Diagnostic products, Process validation for medical devices

Greg Martin - CE Marking Medical Devices with Software

Haydar Jaafar - Drug-Device Combinations

Itoro Udofia - Post Market Surveillance & Vigilance, CE Marking, Compliance to the Medical Devices Directive, Clinical Evaluation, Technical File Writing

Jennifer Durrant - Utilizing Materials of Animal Origin

Stuart Corner - Process Validation

Sue Spencer - In Vitro Diagnostics

Suzanne Halliday  - CE Marking, Compliance to the Medical Devices Directive, ISO 14971 Risk Management, Post Market Surveillance and Vigilance