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Training courses & Webinars:
GMP

 

An Introduction to Pharmaceutical Packaging Training Course

An Introduction to Pharmaceutical Packaging

28-29 Sep 2021 - Online webinar
Also on: 28 Mar 2022

This course provides an essential overview of pharmaceutical packaging and will be valuable for newcomers to this field. It will also act as a good refresher for those with more experience.

Presented by Chris Penfold (bio)

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Common Technical Document Training Course

Common Technical Document

1-2 Dec 2021 - Online webinar
Also on: 1 Feb 2022

A comprehensive review of the regulations and technical requirements for chemistry, manufacturing and control (CMC) management of your application.

Development of Combination Products: Critical Interactions Training Course

Development of Combination Products: Critical Interactions

4-5 Nov 2021 - Online webinar
Also on: 22 Feb 2022

Linking the technical requirements of device design and pharmaceutical product development.
Using QbD to deliver drug/device combinations.

Effective Technology Transfer Training Course

Effective Technology Transfer

5-6 Oct 2021 - Online webinar
Also on: 11 Jan 2022

The ‘how to’ of technology transfer across the product lifecycle

Presented by Bruce Davis (bio)

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Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

18-19 Oct 2021 - Online webinar
Also on: 25 Apr 2022

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Pharmaceutical Packaging, Labelling and Artwork Origination Training Course

Pharmaceutical Packaging, Labelling and Artwork Origination

14-15 Dec 2021 - Online webinar
Also on: 27 Jun 2022

This course has been designed to present a number of important developments in pharmaceutical packaging and labelling from regulations, standardisation and technology to innovation and artwork origination.

Presented by George Barrie (bio)
and 6 more leading experts

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Process Validation with Qualification Training Course

Process Validation with Qualification

21-22 Sep 2021 - Online webinar
Also on: 14 Mar 2022

Gain a comprehensive understanding of the EU and FDA process validation guidance, learn how to establish a process validation programme, understand the link between QbD and process validation, apply relevant tools for process validation including risk assessment.

Presented by Bruce Davis (bio)

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Stability Testing of Pharmaceuticals and Biopharmaceuticals Training Course

Stability Testing of Pharmaceuticals and Biopharmaceuticals

1-2 Dec 2021 - Online webinar
Also on: 14 Jul 2022

Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learn how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.

Presented by Ray Munden (bio)
Allan Watkinson (bio)

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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

The speaker was very clear and enabled participants to ask questions with a lot of patience and with clear answers.

Yaniv Menachem, Regulatory Affairs Specialist, Elcam Medical ACA Ltd.

Very good! Great speaker, well prepared, huge knowledge.

Simone Tortoioli, Technical Project Leader Drug Substance, Idorsia Pharmaceuticals Ltd.

Excellent speaker and allowed enough time to make the course personal to each requirement. Highly recommended

Jitinder Wilkhu, Product Development Lead, GW Pharmaceuticals PLC

Very good.

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

Overall content of the webinar was very good and covered a lot of topics.. The presentation was clear and included a lot of information. I believe this course was very informative and covered a breath of information in regards to combination product and i gained a lot of useful information and knowledge.

Rebekah Coke, Regulatory Affairs Specialist , Bespak Europe Ltd, Recipharm

I feel the content was detailed and informative.

Anisa Mohamed, Regulatory Affairs Officer, Welsh Blood Service

I am very pleased with the webinar.

Astrid Beck Vestergaard, Quality Assurance, Cytovac

I liked Andrew's teaching methods mainly engagement of participant all the way through the course.

Rehab Alnabhan, , Miltenyi Biotec B.V. & Co. KG

Bruce was very engaging, he tailored the course to individual needs and allowed time for questioning to make the course content very relevant to our experience.

Emma Lennon, Senior Manager, Research & Development, GW Pharmaceuticals