Founded in 1982, Quality Assistance is a leading European Contract Research Organisation assisting the pharmaceutical and biotechnology industries with the development and the optimisation of their products.

We are in a position to provide a comprehensive range of services compliant with the highest quality standards required by the EMEA and the FDA.

Total outsourcing

Our daily challenge at Quality Assistance is to fulfil your expectations by finding the best solutions to your problems.

We can provide a complete project management package, from pre-clinical phase to post-approval. At all stages of the process, you will be in direct communication with the appropriate technically competent people.

A multidisciplinary

Our recruitment policy is to engage highly-qualified experienced people. We give them both regular training and ample opportunities to update their skills and knowledge via scientific networking.

This in-house expertise ensures that your projects are dealt with efficiently and reliably. Appropriate partnerships allow Quality Assistance to offer you complementary competencies.

Equipement

In addition to general laboratories, our state-of-the-art premises include BL2 and BL3 laboratories, facilities for handling cytotoxic products, clean rooms (ISO 5 to ISO 8) and stability storage units. Dedicated pre-clinical and clinical sites complete the facilities available.

To keep abreast with latest technologies, we spend around 10% of our annual revenue on equipment. In order to ensure accurate, precise, reliable results, all our equipment is qualified, validated and serviced by a dedicated team from our Quality Assurance department.

Total Quality

As data produced at Quality Assistance are used for regulatory purposes, we have set up appropriate systems to guarantee their quality, confidentiality and security. To ensure compliance with international quality standards (cGMP, GLP, GCP, ISO 17025), 15% of our staff work full-time on the management of these systems.