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Bruce Davis

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Bruce Davis runs his own training/consultancy company for science and risk based approaches to Engineering and Process Validation (PV), Quality by Design (QbD), Quality Risk Management, GMP for Engineers and other related topics. He has run many training events for companies both in the UK and internationally and is often invited to speak at international conferences. He is past Chair of ISPE International Board of Directors and led their case study for practical implementation of QbD. He co-chaired the team updating their Technology Transfer (TT) Guide and carries out training for them and other organisations. He is a professional engineer and has many years’ experience in the pharmaceutical industry and a wide international knowledge, and understanding of current regulatory approaches in the above topics for both US and EU. He previously worked at AstraZeneca, where he had a number of responsibilities, including managing international engineering, facilitating QbD and leading changes to qualification practices. He played a leadership role to set up De Montfort University’s MSc distance learning course in QbD. He is an Associate to NSF Healthsciences, and for them has carried out consultancy and training in the above topic areas, and also for driving down human error.

Process Validation with Qualification Training Course

Process Validation with Qualification

2-3 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.

Process Validation with Qualification Training Course

Process Validation with Qualification

4-5 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.

Effective Technology Transfer Training Course

Effective Technology Transfer

20-21 Apr 2021

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

Effective Technology Transfer Training Course

Effective Technology Transfer

22-23 Apr 2021

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

Process Validation with Qualification Training Course

Process Validation with Qualification

21-22 Sep 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.

Process Validation with Qualification Training Course

Process Validation with Qualification

23-24 Sep 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.

Effective Technology Transfer Training Course

Effective Technology Transfer

5-6 Oct 2021

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

Effective Technology Transfer Training Course

Effective Technology Transfer

7-8 Oct 2021

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