Online training during Covid restrictions - our programes continue this spring in online webinar format
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In-house & bespoke training:
Life Sciences

 

Biopharma

Sample course outlines include:

  • Biosimilars
  • Biotechnology for the Non-Biotechnologist

See all 2 course outlines

Clinical

Sample course outlines include:

  • Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
  • Clinical Quality Management Systems

See all 12 course outlines

Development and technology

Sample course outlines include:

  • An Introduction to the Design and Development of Medical Devices
  • Cyber Security for Medical Devices

See all 9 course outlines

GMP

Sample course outlines include:

  • An Introduction to Pharmaceutical Packaging
  • Common Technical Document

See all 9 course outlines

Medical writing

Sample course outlines include:

  • Effective Technical Writing & Editing
  • Medical Writing for Medical Devices

See all 3 course outlines

Regulatory

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 52 course outlines

Vigilance

Sample course outlines include:

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

See all 14 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, ,

“Excellent!! Speakers were very knowledgeable and approachable.”

Morag Appleton, Pharmacovigilance Manager, Dermal Laboratories Ltd

“All fine”

Jusna Begum, Medical Operations Coordinator, GW Pharmaceuticals PLC

“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

“A very good all round course. I learnt a lot and will take the information away with me to use in my dealings with Medical Devices.”

Jennine Walker, Clinical Affairs Manager, Dermal Laboratories Ltd