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In-house & bespoke training:
Life Sciences

 

Sample course outlines include:

  • Biosimilars
  • Biotechnology for the Non-Biotechnologist

See all 2 course outlines

Sample course outlines include:

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

See all 12 course outlines

Sample course outlines include:

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

See all 8 course outlines

GxP

Sample course outlines include:

  • An Introduction to Pharmaceutical Packaging
  • Common Technical Document

See all 9 course outlines

Sample course outlines include:

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

See all 3 course outlines

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 Europe the USA

See all 52 course outlines

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

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