C37_Mar 2018
Good refresher for the course I took 10+ years ago. Update on regulations and inspector expectations. Practical tips in outsourcing setting - The exercise and possibility to ask questions related to actual operational challenges at own company.
C45_May 2018 (2)
Expected knowledge GDPR reached.Expected a bit more practical training, course was not so much workshop oriented. This was not a problem for me as my main goal was to catch-up on the general GDPR knowledge. Due to the low number of participants, the course was interactive which was very good.
C40_Apr 2018 (2)
Lots of practical real-life examples - nice practical introduction to auditing.
C40_Apr 2018
Good introduction for people new in this field - received lots of good advice for future conduct of Audits and Audit Report writing, as well as helpful advice on how to prepare for Audits - very satisfied - I would like to thank the Trainer for this great course and hope to see her in future
C45_May 2018
The training helped me bridge the gap between the theory of the law and its practical application in our business.
C37_May 2018
Before going to this course "CSV" was a dark bow for me. So with this training and also with the expertise of our trainer, I'm able to understand almost every thing when people are talking about computer system validation - The training was very interesting thanks to Marc. With his expertise, he explains us the trick
C15_May 2018
I had previously worked in a GCP environment, but for some years wasn't active in this field. I now feel more secure and comfortable with the upcoming tasks at Takeda - I really liked the interactive sessions with the questions
C36BRU – Feb 2018 (2)
It is a good overview on the preclinical study required to enter phase I. Comprehensive overview on CMC and toxicology studies.
C36BRU – Feb 2018 (1)
I learned the concept regarding how to set the starting and miximum doses and how to design the dose escalation. The CMC and preclinical requirement, the design of FIH protocol, determination the dose range for FIH clinical trials.
C01LEI – Feb 2018 (2)
It is a well organised course in which all the aspects important for a junior CRA will be explained. Since I am working in the Academic, I thought it was really nice to get more insight in how things are be done in the companies. It was really good, it was a small group of people (6) so