Management Forum courses now available at IPI Academy - visit IPI for an updated experience and a broader selection of courses and subjects

In-house & bespoke training:
Industry

 

Animal Health

Sample course outlines include:

  • A Practical Approach to Veterinary Vaccine Development and Registration in the EU
  • Advanced Veterinary Pharmacovigilance

See all 9 course outlines

Medical Devices

Sample course outlines include:

  • Advanced Regulatory Affairs for Medical Devices
  • An Introduction to the Design and Development of Medical Devices

See all 29 course outlines

Pharmaceutical

Sample course outlines include:

  • A Practical Guide to Producing and Maintaining the PSMF
  • A Practical Guide to Writing Risk Management Plans (RMPs)

See all 57 course outlines

Training options

All of our course outlines are available:
Ready made for any number of participants or With a programme and presenters customised to your requirements
And in your preferred format, or combination:
Face-to-face training at your location or Webinar/interactive online

Previous attendees said...

“Overall, I would recommend the webinar to people who are starting a career in clinical trials as it gives a good overview of all aspects of GCP.”

Laure Bidois, Senior Advisor Regulatory Affairs, knoell

“Great content and discussion. Very good presentation style... Very worthwhile presentation ”

Justine Campbell, Senior Technical Services Veterinaria, QBiotics

“Great for anyone looking to build on their PV Vet knowledge - for beginners and more experienced PV professionals especially in line with the new EU Veterinary Regulations”

Oluwafemi Odugbesan, , Boehringer Ingelheim Vetmedica GmbH

“It was a very useful training that fulfil my necessities about the Industry standards for the Technology transfers... Bruce is very knowledgeable and he was continuously asking the participants to provide feedback and their own experiences.”

Sergio Molina Zaragoza, Vice President Research and Development, Grifols Biologicals LLC

“It was a well done webinar, the speakers were very competent and experienced. The content was informative”

Helena Metzker, Clinical Research Associate, MSD Animal Health Innovation

“I was hoping to achieve more knowledge about combination product and the regulatory documentations needed for the market authorisation and this was completely accomplished.”

Greta Ferrari, Analytical Scientist, Chiesi Farmaceutici

“Well designed course that covers the process in the right amount of detail for different delegates, and was very interactive in getting delegates ideas and comments on areas. Presentation was simple and easy to follow given how much there was to cover, and was very well presented from Declan.”

Liam Aylwin, Internal Audit Manager, Dechra Pharmaceuticals

“Understanding RFP and RFI were achieved, KPI session was very helpful and I learnt about oversight plan which I never knew about... Laura was very good, provided great content of the subject matter and discussions included were good and relevant. ”

Stephanie Yearwood, Senior Vendor Management Coordinator , IQVIA

“I would recommend it to anyone with no experience of design controlled medical device development. A good overview with a good amount of detail.”

Hugh Clark, Mechanical Engineer, Cambridge Design Partnership

“Good pace. Mixture of text and graphics... David did a good job and was engaging considering that the course was online, which is always difficult.”

Danny Kendall, Senior Physicist, Elekta Ltd