DAVID TREW CONSULTING LIMITED
DEVELOPMENT, VALIDATION AND ACCREDITATION OF LABORATORY QUALITY MANAGEMENT SYSTEMS
- Good Laboratory Practice (GLP)
- Good Manufacturing Practice (GMP)
- Good Clinical Laboratory Practice (GCLP)
- Good Clinical Practice (GCP)
- ISO 17025, 9001, 15189
Having robust and effective quality assurance systems in your laboratory is a key requirement of all of these schemes.
However, developing and implementing the required laboratory quality management systems is a significant undertaking. As we have over ten years of experience developing quality management systems for laboratories and can assist and advise you throughout the entire process.
In addition, we can help your laboratory obtain your GLP, GMP or GCP license, or achieve ISO 17025 accreditation.
The quality and reliability of the results delivered by analytical laboratories is of fundamental importance. To achieve global recognition of your analytical results your laboratory will require either licensing or accreditation by one of the international quality assurance schemes, such as:
The above schematic illustrates the general work flow of a typical analytical laboratory, which entails the following steps:
- receiving or obtaining samples
- performing analysis on the samples (employing the managed application of a combination of documented quality management systems, validated analytical methods, qualified laboratory instruments and trained staff)
- and presenting high quality results to your clients
Please click on the links in the schematic to find out more about each service offered.
