Each BSI medical device course is owned by an expert in that field to ensure that we keep material cutting edge, and will be delivered by one of over 60 expert trainers worldwide. Learn more about our expert course owners and their experience, qualifications and specialist subject areas by clicking on the links below.
For more information on the courses, please contact your local BSI office.
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
Linda Moon - ISO 13485, CE marking for In-Vitro Diagnostic products
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
Suzanne Halliday - CE Marking, Compliance to the Medical Devices Directive, ISO 14971 Risk Management, Post Market Surveillance and Vigilance