In-Depth ISO14155:2020 training (Accreditation)
Module 1: Scope
Module 2: Ethics Considerations
Module 3: Clinical Investigation Planning
Module 4: Clinical Investigation Conduct
Module 5: Clinical Investigation Close Out
Module 6: Responsibilities of Sponsor
Module 7: Responsibilities of Principal Investigator
This is what you can expect
"Rianne Tooten knows what she is talking about and can convey the material well and clearly. Her enthusiasm and practical examples in particular help enormously to make the theory practical and understandable. I can recommend everyone to follow this course"
- Maarten Hieltjes, Scientist at Philips Research
Femke Overmars Freelance CTM, srCRA
”What a great training! It was set up that all could be followed with even limited or no medical device experience. A nice extention and refresher on my broad clinical knowledge"
Alberta Huisman, Freelance CRA
"The training is very informative and easy to follow for clinical research professionals with or without Medical Device Trial experience"
Marieke van der A, freelance CRA
“Very well organized training, lots of up to date knowledge and communicated in a good clear way”