Our fields of expertise

Qualilab offers its support to companies in the biotechnology and medical device sectors for control or validation measures, product or process monitoring plans, the preparation of regulatory dossiers, clinical and toxicological evaluations, the implementation of QMS, as well as the performance of quality audits of partners involved in development projects.

Since its creation, Qualilab has focused on meeting the needs of COFRAC-recognized GLP testing facilities by offering Quality Assurance services.

QMS compliance, data review, IS validation, preparation of product information files, toxicological evaluation — Qualilab, an expert in cosmetic standards, is able to work within R&I laboratories and on cosmetic industry production sites, as well as with their suppliers and subcontractors.

QMS compliance, data review, IS validation, preparation of registration dossiers, toxicological evaluation, data analysis — Qualilab, an expert in pharmaceutical standards, is able to work within R&D laboratories, on production and distribution sites in the pharmaceutical industry, as well as with its suppliers and subcontractors.

Subject to increasingly stringent regulations (COFRAC accreditation in accordance with NF EN ISO 15189, HAS certification, etc.), medical biology laboratories and healthcare facilities are facing new requirements.

Through training, auditing, and implementation of the NF EN ISO 17025 standard, Qualilab works with accredited laboratories to guide them towards achieving and maintaining their accreditation. Qualilab has a team composed of experts in their fields.