Brian HammondOver Forty years’ experience in the industry initially in Analytical development moving on to Quality Compliance and System Validation, followed by seventeen years experience in the training and consultancy arena.

Contracts and areas of involvement have included: -

Development of training material, both classroom and e-learning packages, to support the Quality Management System of a major Pharmaceutical Company. Also support during gap analysis following implementation of the QMS.

Development and delivery of cGMP training packages covering a number of disciplines. This included development of suitable packages to be delivered to engineering staff, office and support staff.

Training of entire factory staff, including management, ancillary & admin staff, in the principles of cGMP and how it relates to their role in the manufacture of Pharmaceutical products.

Development and delivery of training material covering a number of different Quality areas. These include Good Documentation Practices, Corrective & Preventive Action (CAPA), Change Control, Root Cause Analysis and cGMP aspects of Engineering Permits to Work.

Troubleshooting Cleaning Validation issues in a small scale Pharmaceutical Development environment.

Development and implementation of a training program to improve the inspection and testing regimes following plant cleaning.

Development and delivery of training material for Cleaning Validation covering all aspects of the task from initiation to final testing and release. This training has been delivered to a number of Company’s within the UK.

Advice on best practices and techniques for training operatives involved in Advanced Swab testing & Visual Inspection Techniques. This project also involved extensive “train the trainer” techniques to allow the Company to maintain the training level in future years.


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