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Training courses & Webinars:
Life Sciences

 

Biopharma

Next events:

  • 29 Sep-1 Oct 2021 Biotechnology for the Non-Biotechnologist
  • 13-14 Oct 2021 Biosimilars

See all 10 courses

Clinical

Next events:

  • 22-23 Sep 2021 Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
  • 24 Sep 2021 GCP and Clinical Research Update - Hot Inspection Topics

See all 40 courses

Development and technology

Next events:

  • 27-28 Sep 2021 Human Factors and Usability Engineering in the Development of Drug Delivery Products
  • 11-12 Oct 2021 An Introduction to the Design and Development of Medical Devices

See all 23 courses

GMP

Next events:

  • 28-29 Sep 2021 An Introduction to Pharmaceutical Packaging
  • 5-6 Oct 2021 Effective Technology Transfer

See all 29 courses

Medical writing

Next events:

  • 24 Sep 2021 Effective Technical Writing & Editing
  • 19-20 Oct 2021 Medical Writing for Medical Devices

See all 13 courses

Regulatory

Next events:

  • 23 Sep 2021 Risk Management for Pharma and Biopharma Professionals
  • 27-28 Sep 2021 Regulatory Affairs for Support Staff

See all 117 courses

Vigilance

Next events:

  • 22-24 Sep 2021 Advanced Pharmacovigilance
  • 8 Oct 2021 Pharmacovigilance Aspects of Licensing Agreements

See all 41 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

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Understanding the Pharmaceutical Industry

£150.00/€210.00/$234.00

Previous attendees said...

“An excellent 2 days - required lots of concentration but worth it. It was very engaging and encouraged me to continue learning and improving.”

Jane Kean, Regulatory Associate, Elanco UK AH Limited

“Very well organized in terms of content, very well presented, replies for every single question is addressed by the wonderful speaker and I truly enjoyed it and learned so much. Thank you it was excellent!”

Nurit Birenboim, Regulatory Affairs Associate, Ayala Pharmaceutical

“Great session, thank you”

Kasia Stathers, Vigilance Officer , Reckitt Benckiser Group

“In depth information delivered clearly from an expert with masses of experience in the field.”

Marketa Slee , Pharmacovigilance Specialist , SOTIO a.s.

“Very good.”

Sylwia Andrzejewska, Stability Coordinator CTM Analytics Austria, CTM Analytics, Valneva Austria GmbH

“Very interactive and stimulating.”

Margherita Lerro, Study Manager, Menarini Ricerche

“Really useful refresher on CAPA and the processes used. It has helped me prioritise and categorise CAPA types, and I found particularly useful the section on risk scoring and utilising the risk register for those classified as minor.”

Claire Crewe, QA Maanger, JensonR+

“I hoped to better understand the content of the PSMF and what is requested during inspections. I definitely think that now I have a deeper insight on that and an overall comprehension of the best solutions to manage the PSMF properly. Very well presented, with a good level of details.”

Giulia Ferrari, PHARMACOVIGILANCE SPECIALIST, Angelini Pharma s.p.a.

“Very clear explanation.”

Gaetano Aiello, Manager, EU/International PV Office, JazzPharmaceuticals

“Greame was clear and concise and answered our questions and gave good examples from his experience. Very enjoyable webinar with lots of content and clearly a very experienced speaker!”

Claire Norman, Safety Advisor, The Boots Company