RQA Member: USD ($) 135.00
Non-Member: USD ($) 176.00
Your Price: USD ($) 176.00
The original co-authors of the Good Clinical Laboratory Practice (GCLP) booklet have collaborated again to produce this excellent training course to assist laboratories and their staff with the implementation of GCLP. Often the first steps of implementing a quality system are the most difficult and this eLearning course provides vital guidance on how to set about implementing GCLP within your own laboratory.
The training will also be beneficial to those who work within a clinical trials laboratory and who need to understand the GCLP requirements and comply with GCP regulations.
The course provides step by step guidance, in 10 modules, on all the major system and process requirements for GCLP compliance. It is an invaluable tool for implementing and maintaining the GCLP quality system. The course can also be utilised as refresher training for those who need reminding of the elements required for compliance.
Once you have successfully completed the assessment (80% pass mark), you will be shown your pass mark and percentage and will then be asked to complete your details to generate a PDF certificate (displaying the CPD points gained) which you can download or print for your records.
Tim Stiles is a Director of Qualogy Ltd, a global consultancy support organisation which provides consultancy on implementation, training, advice, audit and contract regulatory archive services to those working in the GLP, GCP, GCLP and GMP industries.
At the time of publishing Vanessa Grant was the Director of Quality Assurance for Envigo, and was responsible for the organisation of approximately 100 auditors across 9 sites ensuring the effective implementation of the QA programme. This extensive programme covers GLP, GCP, GCLP, GMP and Computer System compliance.
Multi-user licences for corporate use are also available, please click here for prices and further information.
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