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Training courses & Webinars:
Life Sciences


Next events:

  • 11-12 Jan 2022 Biosimilars
  • 7-9 Mar 2022 Biotechnology for the Non-Biotechnologist

See all 7 courses

Next events:

  • 27-28 Jan 2022 Clinical Trial Regulatory Requirements
  • 21-22 Feb 2022 EU Clinical Trial Regulation: Overview and Implementation

See all 29 courses

Next events:

  • 8-9 Mar 2022 Human Factors and Usability Engineering in the Development of Drug Delivery Products
  • 30-31 Mar 2022 Pre-Filled Syringes: End-to-End Processing

See all 13 courses


Next events:

  • 11-12 Jan 2022 Effective Technology Transfer
  • 1-2 Feb 2022 Common Technical Document

See all 21 courses

Next events:

  • 9 Feb 2022 Effective Technical Writing & Editing
  • 6-7 Apr 2022 Medical Writing for Medical Devices

See all 10 courses

Next events:

  • 18 Jan 2022 Filing eCTD Submissions
  • 3-4 Feb 2022 Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union

See all 87 courses

Next events:

  • 13 Jan 2022 A Practical Guide to Writing Risk Management Plans (RMPs)
  • 20 Jan 2022 A Practical Guide to Producing and Maintaining the PSMF

See all 31 courses

Understanding the Pharmaceutical Industry


Very good presentations and discussions. Overall good interactions of participants.

Mario Caiano, PV Operations Unit Support - GVP Compliance Manager, PQE

Both speakers set out their presentations in a clear and easy-to-follow manner, ensuring that a wide range of points were covered. Both answered everyone's questions in great detail which was very helpful and the experience and expertise of each speaker was evident.

Michaela Muller, Safety Scientist, Panacea Pharma Projects Ltd

[The speaker] was very friendly, professional and thoughtful. He encouraged all the trainees to participate in the exercises in a very positive & constructive way.

Grace Jung , Senior Scientist, Design Transfer, Speedx Pty Ltd

Personally I found the training very helpful as I realised how the concept of Data Integrity reflects in my daily work. I understood the big impact of Data Integrity in the Clinical Research which is becoming more and more digital.

Chiara Delmaestro, , Chiesi Farmaceutici S.p.A.

The content was excellent and all presenters were clearly SMEs, who managed to explain much of the complex content in an understandable way.

Sunil Singh, Director, Regulink Ltd

Excellent training session, highly recommended.

Magali Le Goff, Director Scientific Writing & Regulatory Sciences, BlueReg

All round excellent score. David was very clear with his diction and could not be faulted. He clearly has vast knowledge and experience in this field.

Christopher Thorpe, Junior Engineer, Osler Diagnostics

David was very knowledgeable about the course content, and was able to answer all questions put to him throughout the course. David did well to deliver the training via the webinar.

Richard Arthur, Quality Engineer, Occuity

Overall I quite enjoyed the webinar. Everything was thoughtful and easy to perceive. Particularly I liked the part when speaker introduced with the requirements of registration purposes in United States and compared with EU regulations.

Alise Spakevica, , AS Kalceks

This training provided a comprehensive view of what is expected from regulators. [Richard] paid attention to speak clearly (appreciated from not-native English speakers) and was attentive to the participants.

Emmanuelle Tourte, Head of Regulatory Compliance & Data Management, Guerbet