Our latest COVID-19 information - full Autumn programme of webinars now in place

Training courses & Webinars:
GMP

Good manufacturing practices (GMP) are required to conform to the guidelines recommended by agencies that control the authorisation and licensing of the manufacture and sale of pharmaceuticals and medical devices. Our training courses have been designed to ensure that delegates are up to speed with latest developments and best practice.

 

An Introduction to Pharmaceutical Packaging Training Course

An Introduction to Pharmaceutical Packaging

15-16 Mar 2021 - London
Also on: 17 Mar 2021

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

2-3 Jun 2021 - Online webinar
Also on: 9 Jun 2021

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

Presented by Andrew Willis (bio)

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Cyber Security for Medical Devices Training Course

Cyber Security for Medical Devices

19-20 Apr 2021 - London
Also on: 21 Apr 2021

Data Integrity and Document Management Training Course

Data Integrity and Document Management

4 Mar 2021 - London
Also on: 5 Mar 2021

Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.

Presented by Laura Brown (bio)

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Development of Combination Products: Critical Interactions Training Course

Development of Combination Products: Critical Interactions

5-6 May 2021 - Online webinar
Also on: 11 May 2021

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

Presented by Andrew Willis (bio)

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Dry Powder Inhalers Training Course

Dry Powder Inhalers

23-24 Jun 2021 - London

A comprehensive overview of DPIs including market trends, treatments formulation, regulation and device design

*FULLY UPDATED PROGRAMME*

Presented by Mike Holroyd (bio)
David Howlett (bio)
Helen Muirhead (bio)

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Effective Technology Transfer Training Course

Effective Technology Transfer

20-21 Apr 2021 - Online webinar
Also on: 22 Apr 2021

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

Presented by Bruce Davis (bio)

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How to Write Effective SOPs (Standard Operating Procedures) Training Course

How to Write Effective SOPs

3 Dec 2020 - Online webinar
Also on: 28 Jun 2021

An essential course for ensuring compliance with regulatory requirements which will be of particular relevance for pharmacovigilance, regulatory affairs, clinical research/operations, GMP, QA and document management functions.

Presented by Laura Brown (bio)

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Improving Processes and CAPA (Corrective and Preventative Action) Training Course

Improving Processes and CAPA (Corrective and Preventative Action)

4 Dec 2020 - Online webinar
Also on: 29 Jun 2021

This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA.

Presented by Laura Brown (bio)

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Injectable Drug Delivery Training Course

Injectable Drug Delivery

10-11 Mar 2021 - London

Advances in technology for pens, auto-injectors, large volume pumps, patch pumps, needle-free, pre-filled syringes and other parenteral methods.

Presented by Patrick Anquetil (bio)
and 6 more leading experts

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Metered Dose Inhaler (MDI) Technology Training Course

Metered Dose Inhaler (MDI) Technology

16-17 Feb 2021 - Online webinar
Also on: 18 Feb 2021

A comprehensive overview of MDIs including development, manufacture, regulation and market potential

Presented by David Howlett (bio)

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Nasal Drug Delivery Training Course

Nasal Drug Delivery

15-16 Apr 2021 - London

A comprehensive review of the latest scientific developments, technology advances and regulatory guidance in the field of nasal drug delivery.

Presented by Michael Benninger (bio)
and 13 more leading experts

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Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

22-23 Mar 2021 - Online webinar
Also on: 29 Mar 2021

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

Presented by Andrew Willis (bio)
Alison Wilson (bio)

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Pharmaceutical Packaging, Labelling and Artwork Origination Training Course

Pharmaceutical Packaging, Labelling and Artwork Origination

27-28 Oct 2021 - London

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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Pre-Filled Syringes: End-to-End Processing Training Course

Pre-Filled Syringes: End-to-End Processing

23-24 Mar 2021 - Online webinar
Also on: 25 Mar 2021

Topics such as quality of syringe manufacture, quality of syringe components and why, quality of filling (volume check, reject reduction), quality of inspection and product release will be discussed in detail.

Presented by Dale Charlton (bio)
and 3 more leading experts

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Process Validation with Qualification Training Course

Process Validation with Qualification

2-3 Mar 2021 - Online webinar
Also on: 4 Mar 2021

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

6-7 Jul 2021 - Online webinar
Also on: 8 Jul 2021

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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Really informative with a good overview of the guidelines and enough real-life examples and exercises to maintain engagement. I reinforced my understanding and gained confidence in designing stability studies efficiently and correctly.

Celia Garland, Medical Affairs Officer, Hameln Pharmaceuticals Ltd

There was great insight given into the background of stability and why it is so important. I would recommend this course to the rest of my team at work.

Yasmin Khimji, QC Analytical Scientist, MeiraGTx

Excellent presentation by a first-class speaker who has a wealth of knowledge. I particularly liked the interactive exercises.

Wil Pantin, New Product Introduction Manager, M & A Pharmachem Ltd

Great speaker, capable of transmitting his knowledge in an enjoyable and interactive way.

Rocio Arias, Regulatory Affairs Technician , Pharmex Advanced Laboratories, S.L.

It was one of the best workshops I have attended: content was according to expectations, all questions were answered, presenter was passionate and kept the energy high during the presentations.

Iris Vanwelkenhuysen, CMC Dossier Leader, Galapagos

Excellent.

Hannah Allende, Assistant Clinical Trials Manager, University Hospitals Plymouth NHS Trust

A very talented speaker.

Mario Mohos, Quality Supervisor, Mylan Hungary Kft

Excellent course, highly recommended.

Hannah Allende, Assistant Clinical Trials Manager, University Hospitals Plymouth NHS Trust

The course was absolutely great and to get helpful advice from the experienced speaker was fantastic.

Ulrike Ratz, CMC Manager, Cheplapharm Arzneimittel GmbH

Excellent teacher. Laura presented in an inclusive way and her presentation kept my attention.

Annette Hjemsted, PV Specialist, H. Lundbeck A/S