The Ideal Partner for the Life Science Industry
The ATP-CGPharm Group contributes every day to ensuring medical product quality, patient safety and strict compliance with regulatory requirements by supporting improvement of the manufacturing processes and quality programs of its clients.
The Group offers a broad range of services in GxP engineering, commissioning, qualification validation, quality assurance, quality control and environmental monitoring. ATP-CGPharm Group operates internationally with offices in France and Switzerland. The company has a proven track record of successfully completed projects and is renowned for completing projects in-spec, in-time and in-budget.
THE KEY FIGURES OF THE ATP-CGPharm GROUP:
on permanent contracts
The ATP–CGPharm Group’s strenghts :
Knowledge and Experience:
ATP-CGPharm Group has more than 20 years of experience and a proven track record in technical and GxP-compliance consulting, qualification and validation and in design, planning and realization of plant and facility projects.
Availability of Resources:
All our employees are employed on a permanent basis. This and an extremely low staff attrition make it possible to provide lasting support to our partners.
Multidisciplinary and Multilingual skills:
Communication and Decision Making:
ATP-CGPharm Group is managed by its owner which simplifies communication, grants an exceptionally high responsiveness and ensures fast decision making.
A unique partner network provides the ATP-CGPharm Group to access to additional resources and technical expertise, especially in the area of engineering.