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GMP

9 courses in this category:

25 Apr 2018
EUR 979.00
GBP 699.00
USD 1090.00

An Introduction to Pharmaceutical Packaging

This course provides a good basic grounding and appreciation of what is required for the packaging of pharmaceutical and healthcare products. It is ideal for newcomers and a good refresher for those with more experience

Full details

5-6 Dec 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
4 Jul 2018

Common Technical Document

Gain a clear understanding of the regulatory and technical requirements for CMC management of your full and generic application in major markets of EU and USA. Global roll out of the dossier to ROW regions including LATAM, ASEAN, MENA and CIS territories also covered.

Full details

6 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
28 Jun 2018

How to Write Effective SOPs

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

Full details

7 Dec 2017
EUR 979.00
GBP 699.00
USD 1090.00

Also held on:
29 Jun 2018

Improving Processes and CAPA (Corrective and Preventative Action)

This meeting 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

Full details

26-27 Apr 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Pharmaceutical Development of ATMPs

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

Full details

2-3 May 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Pharmaceutical Packaging, Labelling and Artwork Origination

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

Full details

6-7 Mar 2018
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
16 Oct 2018

Process Validation in the US and EU

Gain a comprehensive understanding of the EU and FDA Process Validation Guidance, how to establish a Process Validation Programme, understand the link between quality by design and process validation, apply relevant tools for process validation including risk assessment

Full details

5-6 Dec 2017
EUR 2099.00
GBP 1499.00
USD 2338.00

Also held on:
4 Jul 2018

Stability Testing of Pharmaceuticals

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

Full details

Keeping Up-To-Date as a (GMP) Qualified Person

Keeping up-to-date as a Qualified Person, refresher and intermediate training. A Continuing Professional Development (CPD) workshop for GMP QPs. Providing up-to-date and detailed guidance for current, trainee and returning QPs, to help you fulfil your duties effectively and efficiently in the pharmaceutical Industry.

Full details