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

In-house & bespoke training:
Industry

 

Animal Health

Sample course outlines include:

  • A Practical Approach to Veterinary Vaccine Development and Registration in the EU
  • A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China

See all 13 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 32 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 67 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...

“Presentations/content and speakers were well rounded and provided valuable information for my job that showed the experience they had to give me confidence in the information provided. The whole program, process and all was well worth the cost and time. I will recommend to others - already have!”

Angela Turner, Associate Director GRA,

“I got what I hoped for - i.e. an introduction to the types of documents I will come across, how to select the right content, and how to write it. On top of this, it was extremely useful for me to receive all the little tips and tricks. I think all presenters were very generous in sharing their experience. This includes how to manage difficult stakeholders, when to stick to guidelines and when to use common sense, where to find links on correct use of English, and even be able to ask questions in the future on how to present data.”

Lone Helboe, ,

“I wanted to get some hints and tips on general improvements in writing style when compiling regulatory dossiers - and interested to know more about the required content in the clinical section of the eCTD, which I believe was delivered.”

Judith Rowland, Senior Regulatory Affairs Manager, Nerudia Limited

“Good, engaging and knowledgeable speakers.”

Marit Sorum, Regulatory Affairs Manager, Pharmaq

“I was really satisfied with the webinar. It reflected my expectations and it addressed my needs.”

Roberta Grimaldi, Clinical research principal scientist, GSK

“Very informative”

Shaun Phillips, Eng manager, Renfrew group

“Very good. A lot of information delivered clearly.”

Michael Phillips, Design Development Director, Renfrew Group

“I've really enjoyed this webinar, covering all I was looking for in a short amount of time while keeping it very interesting and interactive along the way. Laura was very impressive, going through a lot of material and always keeping it very interesting. Case studies were very interesting. I also appreciated the use of different interactive tools for exercises.”

Audrey Dicaire-Lavigne, Pharmacovigilance Leader, Jubilant Draximage Inc.

“Very good I enjoyed it, right amount of time and info delivered. Very good interaction with the speakers and all the participants who were from very various backgrounds.”

Eric Helmer, Director Clinical Pharmacology, Galapagos

“The course greatly matched my expectations and it was an invaluable experience, enriching my understanding and providing me with a toolkit to work on in my career.”

Vasileios Eftychidis, Knowledge Transfer Associate - NeuroOncology, Cardiff University