DAVID TREW CONSULTING LTD
Chemistry Services
Creating a quality management system that is both suitable for your laboratory’s needs and meets the requirements of the ISO/IEC 17025:2017 International Standard is a significant undertaking, which requires both a clear understanding of the International Standard, together with experience of laboratory operations.
With over 25 years of experience of working in chemistry laboratories and over five years of consultancy experience, I can develop a QMS suitable for your laboratory’s needs and prepare the associated documents for a fixed price.
The objective of this package is to achieve a successful first stage review by the accrediting body.
The overall process consists of:
- Two day on site gap analysis and report (can be longer if needed)
- Preparation of quality manual, set of quality policies, procedures and forms
- Preparation of test or calibration methods for which the laboratory is seeking accreditation
- Two day on site review of draft documents (can be longer if needed)
- Proofreading of all documents
- Presentation of documents in both electronic and hard copy format
- Two day preassesment audit
- Attendance at assessment (subject to acceptance by the accrediting body)
To discuss your specific needs please click on the link below
Clause 8.1 of the ISO/IEC 17025:2017 International Standard requires the laboratory to establish a quality management system suitable for its needs, which underpins all of its operations.
Quality Management Systems
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