Training courses & Webinars:
Animal Health

“Excellent. I was hoping to refresh, add to and update my knowledge. The webinar was excellent to remind me of areas that I had been involved with many years ago and add knowledge that is more relevant to my role now. I found the topics of the workshop particularly relevant.”

Mary-Ann Tite, Regulatory Manager, Pets |Choice

“It was well laid out and formatted especially for myself who does not have a regulatory role currently. I was hoping to achieve a firmer understanding and overview of submission within the EU, and believe I achieved this. [Speakers] were very knowledgable and provided great answers to all questions— supportive but challenged us when doing the workshop. I liked all areas of the course.”

Louise Dunn, Pharmacovigilance and Technical advisor, Zoetis

“Fantastic webinar! Speakers were very knowledgeable, clear, concise, and open to questions at any time—providing in depth background information were appropriate as well. The content was very interesting and I think a very good amount was covered considering the timescales. I enjoyed the workshop a lot. I thought it was a good way to try and put into practice what we had learnt during the webinars. I also thought a very good amount of information was covered for an introduction into the sections of the dossier.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“My goal was to gain a deeper awareness and understanding of what is required in the different sections of a dossier for submission in the EU. I think the course definitely accomplished this and there was lots of useful information, which was very well explained. I can confidently say that I left knowing a lot more than I initially thought I would.”

Emilija Stabingyte, Regulatory & Quality Coordinator, Zoetis UK Limited

“I wanted to have a synthetic overview of part 3 and 4 and wanted to have the clue to build a relevant and efficient clinical development plan.. Very good opinion of content, presentation and speaker.”

Pierrick BOLON, R&D Clinical Manager, Boehringer Ingelheim

“Excellent. Hoped to achieve better understanding of clinical and quality parts of the dossier and this was very well accomplished. ”

Päivi Jutila, Regulatory Affairs Manager, Vetcare Ltd

“Very content with the course! The length of each chapter was nicely timed, breaks were ideal. The case we studied was a very good way to summarize all the information [seen] and it generated a lot of interesting questions/dilemmas. I would recommend.”

Emma Vanmechelen, Regulatory Affairs Specialist, DeLaval

“The content was very thorough, the presentations were held in an encouraging way and the speakers had impressive knowledge of their area and were very helpful. All [their].presentations were very valuable.”

Bernadett Riszne Ladanyi, QA Specialist/Auditor, Ceva-Phylaxia

“I enjoyed it and learned a lot. The slides are very useful reference material for later.. Nothing too lengthy so everyone could stay very focused. All speakers are very pleasant, friendly and approachable. All parts were very interesting and relevant. Mission was accomplished!”

Yannique Jacobs-Renac, Projectleader, Royal GD

“Very good general training well documented. Overall, all Very good.”

Claire Biener-Milard , RA manager, Boehringer Ingelheim