ATP-CGPharm Group
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.
100
%
Loyal
Customers
20
+
years
of longevity
100
%
Employees hired
on permanent contracts
OUR SERVICES
What we do?
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.
Facility and Process Engineering
For more than 20 years, the ATP-CGPharm Group has been offering tailor-made solutions for the creation of new facilities as well as for the renovation or extension of existing installations.
Staff Leasing
Since 2015, the ATP-CGPharm Group has obtained an authorization for the furnishing of qualified temporary staff in Switzerland in the fields of the Pharmaceutical Industry, Biotechnology, Medical Devices and the Food Industry.
GMP and Compliance
ATP-CGPharm Group offers a broad range of QA, QC and technical compliance support and consulting services.
Qualification and Validation
The ATP-CGPharm Group offers a broad range of qualification and validation services according to the newest international standards.
GMP Digital Solutions
For more than 20 years, ATP-CGPharm has been supporting clients in the Life Science Industry with a broad range of services in GxP engineering, commissioning, qualification and validation, quality assurance, quality control, environmental monitoring, and data analytics.
Key strength
The ATP–CGPharm Group’s strenghts
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.
Pilot Plants & Production Facilities
Tailored solutions for the manufacturing of biotech products, APIs, non-sterile and sterile dosage forms, and medical devices.
Communication and Decision Making
ATP-CGPharm Group's owner-managed structure enables quick decision-making, and streamlined communication.
Multidisciplinary and Multilingual skills
ATP-CGPharm Group leverages the diverse expertise of pharmacists, engineers, and technicians from various cultures.
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.
Management
ATP-CGPharm Group leverages over 25 years of technical and GMP expertise, led by CEO Dr. Christophe Gryczka, a seasoned leader in the pharmaceutical industry.
Partner Network
A unique partner network provides the ATP-CGPharm Group to access to additional resources and technical expertise, especially in the area of engineering.
Careers
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.
Real-World Results
Challenge: The client struggled with manual processes that were time-consuming and prone to errors, affecting product consistency and speed.
Solution: Our team implemented automated solutions for key production processes, including real-time monitoring and data logging systems. We customized the automation to meet the client’s specific needs and ensured that all systems were GMP-compliant.
Outcome: The client saw a 25% increase in production capacity, reduced human error, and improved product quality.
Challenge: The client struggled with manual processes that were time-consuming and prone to errors, affecting product consistency and speed.
Solution: Our team implemented automated solutions for key production processes, including real-time monitoring and data logging systems. We customized the automation to meet the client’s specific needs and ensured that all systems were GMP-compliant.
Outcome: The client saw a 25% increase in production capacity, reduced human error, and improved product quality.
