Medical Device – Toxicological Asssesment and Risk Analysis
We are pleased to invite you to come and hear SAXOCON’s CTO Anders Permin review Medical Device – Toxicological Asssesment and Risk Analysis.
The course will review the following:
– What is regulatory toxicology?
– Which guidelines are used and why?
– Examples of test programs
– Collection of data for risk assessment
– Exercises in the composition of test programs
– Discussion and conclusion
Date: April 23, 2018
Time: 9:00 – 15:30
Venue: Scion DTU, Meeting room M1 , Diplomvej 381, 2800 Kgs. Lyngby, Denmark