Testimonial Archive - Page 24 of 38 - ECCRT
  /   (Page 24)

  I learnt about the clinical trial cycle, abbreviations related to pharmaceuticals (given I come from medical device industry this was new), and budgeting / timesheets / forecasting - Same agenda / timeframe of closeout meeting. Strategies for moderating effective Lessons Learned meetings Unanticipated trial closure procedure (e.g. study stopped for unethical reasons, unblinding procedure, extent to

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.

 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

User registration

Reset Password