The Pharmaceutical Industry is regulated by government agencies such as  MHRA and FDA  to minimise the risk of errors and omissions in the manufacture of Medicinal Products, which might have serious consequences for the health of users of the Products. 

The regulatory agencies achieve their objectives by the enforcement of Good Manufacturing Practice (GMP) regulations.  They control the licensing and manufacture of Medicinal Products and inspect pharmaceutical manufacturing sites for compliance with GMP requirements.  

Authorities around the world require that employees in Pharmaceutical industries should be trained in the disciplines of GMP and their application at all stages of the manufacture of Medicinal Products.   

The training courses offered by HartfordPharma are designed to instruct delegates in the requirements of GMP and to develop a high level of personal responsibility for their implementation.  All courses offer the chance to ask questions and raise issues in a learning environment in which the experiences of the instructor and of other people on the course can be fully utilised.      

The interactive nature of the courses and small group activities, encourages discussion and builds working relationships.  Great emphasis is laid on the importance of good documentary practices; personal responsibility; technical understanding and the limitation of contamination by good personal hygiene and behaviour.

Courses are offered at all levels – for operators, supervisors, technical and administrative support staff, and managers.  Each group is catered for with regard to educational background and understanding.

 The following courses are available:

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Last modified: July 11, 2004