Upcoming TrainingRegister Interest
Upcoming training programs
New dates will be announced here
Register your interest in a program and we will let you know as soon as the next session is scheduled. Our most recent session was the ETO Sterilization Validation Training led by Mr. Viral Sheth.
Who it is for: Medical device manufacturers, regulatory affairs professionals, quality assurance teams, and other industry personnel.
Training catalogue
These programs are available on request. Choose a program to book a session for your team; we will confirm the schedule and delivery format with you.
ISO 13485 – QMS and MDSAP Requirements
Enquire for your team
Risk Management as per ISO 14971
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Clinical Evaluation of Medical Devices
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Biological Evaluation of Medical Devices
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Design and Development of Medical Devices
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EU MDR 2017/745 Awareness
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EU MDR Technical Documentation (Annexes I, II and III)
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Premarket Notification – US FDA 510(k)
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Labelling, UDI, GUDID, Basic UDI-DI and EUDAMED
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Ethylene Oxide Sterilization Validation
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Gamma Radiation Sterilization Validation
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Reprocessing of Medical Devices and Validation
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Microbiological Practices: GLP, Sterility, Bioburden, BET Testing and Method Validation
Enquire for your teamCorporate Training
Book a Training Session for Your Team
Tell us which programs you are interested in, how many participants you expect and when you would like the training. Our team will get back to you to confirm the details.
