Course participant reviews for PTI

Average rating 4.8

Based on 310 reviews.
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5/5
Anonymous
07 Jun 2016

“There was clear information about classification, requirements and exercises.” Regulatory Affairs Team leader, Teva Pharma Nederland

5/5
Anonymous
01 Jun 2016

“It was a very thought provoking course.” Regulatory Affairs Manager, Mundipharma

4/5
Anonymous
24 May 2016

“Good overview for me as a non-regulatory specialist.” Product Development Manager, Certis Europe

4/5
Anonymous
23 May 2016

“Nadine had a lot of experience from work that she shared with us.” QA Specialist, Sobi

5/5
Anonymous
23 May 2016

“The knowledgeable trainer and the discussions was excellent.” Director of Bioassays, Sobi

4/5
Anonymous
19 May 2016

“I enjoyed the content and the way it was presented.” Regulatory Affairs Senior Specialist CMC, GSK Vaccines

4/5
Anonymous
19 May 2016

“The course gave me a great overview and helped me to find materials.” Senior Scientist, MSD Nederland

4/5
Anonymous
19 May 2016

“The organisation of data and the knowledge of the lecturer was great.” Research Scientist, BTG plc

5/5
Anonymous
11 May 2016

“The trainers adjusted the content/order of the presentations to suit those on the course. I took this course as we plan to submit our first Ectd this coming September.” Regulat...

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4/5
Anonymous
11 May 2016

“The global aspect attracted me.” Regulatory Operation System Manager.” Bio Products Laboratory Ltd.

5/5
Anonymous
09 May 2016

“I enjoyed the hands-on sessions most. I wanted to learn about Module 3. It was a very good course; I learn a lot.” Regulatory Affairs Manager, Fresenius Kabi UK

4/5
Anonymous
21 Apr 2016

“I enjoyed the practical exercises most; there was a lot of information.” Regulatory Affairs Specialist

5/5
Anonymous
21 Apr 2016

“Excellent content – very informative. Lots to take away and put into practice.” Senior Manager, Global regulatory Affairs, AngioDynamics Inc

4/5
Anonymous
21 Apr 2016

“It gave me a good overview of registration requirement in Russia/CIS.” QARA Leader Iberia, Zimmer Biomet

5/5
Anonymous
21 Apr 2016

“Very extensive comprehensive content. Local Russian perspective – interesting & informative of marketing and understanding of CIS changes coming up especially in Russia.” Senio...

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4/5
Anonymous
21 Apr 2016

“Very good examples and there was a good overview of the CIS market in general.” Regulatory Affairs Specialist, Varian Medical Systems UK Ltd.

5/5
Anonymous
06 Apr 2016

“The trainer was fantastic; very knowledgeable.” CMC Regulatory Specialist, Concordia International Corp

4/5
Anonymous
06 Apr 2016

“The trainer is excellent and is top of their field. ” Regulatory Officer, Food and Drugs Authority ( FDA ) Ghana

4/5
Anonymous
06 Apr 2016

“The trainer was very knowledgeable and the whole course was very interactive. I believe I have benefited from this course.” Food and Drugs Authority ( FDA ) Ghana

4/5
Anonymous
06 Apr 2016

“I enjoyed the fact that the trainer shared her experience.” Vice President of Regulatory Affairs, K2M Group Holdings Inc

4/5
Anonymous
06 Apr 2016

“The content was delivery to all the audience’s needs and the tutor was very flexible. The course was relevant to my needs and there was time for questions including ones that w...

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4/5
Anonymous
06 Apr 2016

“The general understanding and hands-on experience given in the course was very useful.”

5/5
Anonymous
06 Apr 2016

“The course material was very comprehensive, with a good mix of information on regulations and guidance’s and practical advice on how to comply. I enjoyed the informal atmospher...

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5/5
Anonymous
06 Apr 2016

“The run-through of a template CER was particularly useful.” Clinical Project Scientist, J R I Orthopaedic Ltd

5/5
Anonymous
06 Apr 2016

“CER discussions were great. I learnt a lot.” Product Performance Engineer, K2M Group Holdings Inc

Displaying 226-250 of 310 reviews
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