ATP-CGPharm Group is a GMP consulting and pharmaceutical engineering company with over 30 years of expertise serving the Life Science industry in France and Switzerland.

We support pharmaceutical, biotech and medical device companies at every stage of their development, from facility design and qualification to regulatory compliance and digital transformation.

Our core services include :
- GMP Consulting & Regulatory Compliance (QA, QC, audits)
- Qualification & Validation (IQ, OQ, PQ, FDA, EMA, Swissmedic)
- Facility & Process Engineering (cleanrooms, APIs, sterile manufacturing)
- GxP Digital Solutions (AI, machine learning, data validation)
- Pharmaceutical Staff Leasing 

ATP-CGPharm Group operates internationally with a multilingual team of pharmacists, engineers and GxP specialists.

ATP-CGPharm Group

This department ensures that products and processes meet regulatory standards and internal quality benchmarks.

Validation and Compliance

This department provides expert guidance and project management across various consulting functions.

Consulting Services

This department oversees project management and compliance within engineering initiatives.

Engineering Management

This department focuses on the qualification and validation processes to ensure compliance and quality standards.

Qualifications and Validation

This department focuses on developing and implementing AI technologies and solutions.

ATP-CGPharm Group

Org chart

Teams

Validation and Compliance

Consulting Services

Engineering Management

Qualifications and Validation

Artificial Intelligence

Offices

ATP-CGPharm Group

Org chart

Teams

Validation and Compliance

Consulting Services

Engineering Management

Qualifications and Validation

Artificial Intelligence

Offices

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