Online training during Covid restrictions - our programes continue this spring in online webinar format

In-house & bespoke training:
Industry

 

Pharmaceutical

Sample course outlines include:

  • Drafting and Managing Pharmaceutical Safety Data Exchange Agreements
  • Drafting and Negotiating Clinical Trial Agreements

See all 6 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...

“Great course. Intense but good opportunity to learn and well presented. I enjoyed he group work and chatting to everyone too.”

Feargal Cosgrove, Licensing Manager – Research & Impact, University of Ulster

“Laura Brown was really dynamic. She used good examples and support and I was pleasantly surprised to see a good interaction in the group. ”

Laura Champion, Principal Drug Product Development Scientist, MedinCell

“This course was brilliant and covered all the key points. The speakers were highly knowledgeable and had practical insights and fresh perspectives on drafting issues and implications. Having multiple speakers allowed for a fresh and dynamic course, and increased the amount of information absorbed.”

James Langston, Contracts Manager, AstraZeneca

“Overall it was a very interesting course with much knowledge and very useful techniques for strategic thinking. I really enjoyed the case studies and working in teams to accomplish the exercises. Very well done and very well organised.”

Theofanis Mantourlias, Senior Manager Formulation Development, Fresenius Kabi Austria GmbH

“Very good, good set of strategic analysis tools was given..”

Andreas Gallei, Head of Swine Virology, BIVRC GmbH & Co KG

“Good overview of content, great organisation.”

Amish Unka, Legal Counsel, Morningside Healthcare Limited

“The training is very useful and gives a good and concrete overview of CTAs. Both speakers were willing to explain and answer all questions we had during the training and were very professional and approachable. The course contains the relevant topics and has a good balance between the theoretical part and the practical part. ”

Tinneke De Boeck, Junior Legal Counsel, Galapgos NV

“The speakers were perfect – really qualified and experienced.”

Anne-Caroline Béraud, In House Legal Counsel, Erytech Pharma

“Both the content and the speaker show a high level for the topic 'Pharma project management'. ”

Elena Núñez, Pharmaceutical Development Manager, Takeda

“The guest speakers were a good addition. Overall, well done.”

Katie Sippel, Director, Quality Compliance, Novocol Pharmaceutical of Canada Inc.