Testimonial Archive - Page 19 of 33 - ECCRT
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 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. 

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

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

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

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. 

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

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