About us
20+years of Impact in Life Science Industry
ATP-CG Pharm Group offers broad range of services in GxP engineering, commissioning, qualification validation, quality assurance, quality control and environmental monitoring.
100
%
Loyal
Customers
20
+
years
of longevity
100
%
Employees hired
on permanent contracts
Our Journey
Our Journey Towards Excellence
ATP and CGPharm were founded as separate entities—ATP in 1996 in Switzerland, specializing in engineering manufacturing plants, and CGPharm in 1998 in France, focused on GMP Compliance consulting. Recognizing the need to address the growing complexity of pharmaceutical regulations, the two companies formed a strategic partnership. This collaboration expanded CGPharm’s capabilities, including the acquisition of LBE (1999) and the creation of PharmaControl (2002) to enhance quality control services.

ATP (1996) - Switzerland
ATP was founded in 1996 in Switzerland, specializing in engineering manufacturing plants. It quickly gained recognition for its expertise in pharmaceutical engineering.

CGPharm (1998) - France
CGPharm was established in 1998 in France, focusing on GMP compliance consulting for the life sciences industry. CGPharm’s expertise contributed significantly to ensuring pharmaceutical operations met the highest standards of regulatory compliance.

Strategic Partnership Formation
1999-2004: Expansion of Services
Recognizing the growing complexity of pharmaceutical regulations, ATP and CGPharm formed a strategic partnership to expand their capabilities. This included the acquisition of LBE in 1999 and the creation of PharmaControl in 2002 to enhance their quality control services.

Merger to Form ATP-CGPharm Group
2006: United for Excellence
ATP was founded in 1996 in Switzerland, specializing in engineering manufacturing plants. It quickly gained recognition for its expertise in pharmaceutical engineering.

ISO 9001:2015 Certified Quality Commitment
Since our inception, client satisfaction has been our top priority. We approach every project with precision, expertise, and transparency, maintaining a focus on continuous improvement to ensure compliance with all regulatory standards.
Our ISO 9001:2015 certification reflects our unwavering commitment to delivering consistently high-quality services in a structured and efficient manner. This certification underscores our ability to understand and anticipate our clients' needs, offering tailored solutions that drive success.

Dr. Christophe GRYCZKA
Owner CEO
Meet our Founder
The ATP-CGPharm Group is led by its founder, Dr. Christophe GRYCZKA, a Pharmacist and Pharmaceutical Industry Consultant with over 30 years of experience.
Drawing from his extensive background in managing companies specializing in quality control and medical device production, Dr. Gryczka approaches every project with the same dedication as if it were his own. His goal is always to provide the best GxP-compliant solutions at the most cost-effective prices.
Dr. Christophe GRYCZKA is a trusted partner to our clients, known for his unique leadership style. In addition to guiding the company, he remains actively involved as a project consultant. This hands-on approach ensures he stays deeply informed about GMP regulations, technological advancements, and industry changes, further enhancing the expertise he brings to every project.
























Our Values
Values that Drive ATP–CGPharm
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.

Progress
We are committed to continuous progress, embracing innovation to meet the evolving needs of the pharmaceutical industry and stay at the forefront of compliance, engineering, and quality assurance.

Integrity
Integrity is at the core of our business. We provide transparent, ethical services, ensuring accountability and trust in everything we do.

Satisfaction
Client satisfaction is our priority. We focus on understanding and exceeding client needs, delivering tailored solutions that foster long-term, trusting relationships.

Responsibility
We take full responsibility for our work, ensuring the highest standards of quality and compliance to support the success and safety of our clients’ operations.

Flexibility
We adapt quickly to industry changes and client needs, offering flexible, tailored solutions that keep our clients agile in a dynamic market.
Meet the experts
Our team is composed of diverse, highly skilled professionals, including pharmacists, engineers, and technicians from 10 different nationalities. Fluent in English, German, and often French, we combine youth and experience to continuously improve our expertise. Regular knowledge-sharing ensures the highest quality service in engineering, qualification validation, quality assurance, and environmental monitoring. We provide qualified, permanent staff, offering lasting, tailored solutions with a commitment to excellence and low staff turnover.
