Online training during Covid restrictions - our programes continue this spring in online webinar format
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Training courses & Webinars:
Life Sciences

 

Next events:

  • 29 Sep-1 Oct 2021 Biotechnology for the Non-Biotechnologist
  • 5-6 Oct 2021 Biosimilars

See all 4 courses

Next events:

  • 5-6 Jul 2021 Clinical Trial Regulatory Requirements
  • 20-21 Sep 2021 Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

See all 19 courses

Next events:

  • 13-14 Sep 2021 Metered Dose Inhaler (MDI) Technology
  • 15-16 Sep 2021 Metered Dose Inhaler (MDI) Technology

See all 6 courses

GMP

Next events:

  • 6-7 Jul 2021 Common Technical Document
  • 12-13 Jul 2021 Stability Testing of Pharmaceuticals and Biopharmaceuticals

See all 17 courses

Next events:

  • 23 Sep 2021 Effective Technical Writing & Editing
  • 24 Sep 2021 Effective Technical Writing & Editing

See all 6 courses

Next events:

  • 28 Jun 2021 Best Practice for Writing Effective SOPs
  • 28-29 Jun 2021 Pharmaceutical Regulatory Affairs in the Middle East

See all 55 courses

Next events:

  • 23-24 Jun 2021 Advanced Veterinary Pharmacovigilance
  • 28 Jun 2021 A Practical Guide to Writing Risk Management Plans (RMPs)

See all 18 courses

Understanding the Pharmaceutical Industry

£150.00/€210.00/$234.00

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