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

Training courses & Webinars:
Industry

 

Animal Health

Next events:

  • 23-24 Jun 2021 Advanced Veterinary Pharmacovigilance
  • 12-13 Oct 2021 Introduction to Veterinary Pharmacovigilance

See all 13 courses

Medical Devices

Next events:

  • 30 Jun-1 Jul 2021 Medical Device Regulations in the Middle East and North Africa
  • 5-9 Jul 2021 The Medical Device Summer School - From Concept to CE Marking

See all 34 courses

Pharmaceutical

Next events:

  • 28 Jun 2021 A Practical Guide to Writing Risk Management Plans (RMPs)
  • 28 Jun 2021 Best Practice for Writing Effective SOPs

See all 93 courses

In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Self-paced online courses

More...

The Pharma 'Mini-MBA' On-line Learning Programme

£350.00/€490.00/$546.00

Understanding the Pharmaceutical Industry

£150.00/€210.00/$234.00

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