CPC Achievements

USFDA Inspections
International Audits
DMF Submissions
Projects

Inspections-USFDA, EDQM, EU(GMP), WHO, MHRA, MCC, TGA

CPC provides solutions to multidisciplinary Quality & Regulatory issues concerning Facilities; cGMP; Quality systems & procedures; Regulatory submissions; Compliance. We are also APIC certified auditors and carry out audit of API and Formulations on behalf of US and European companies.

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Quality Consultants

We are specialists in providing end to end quality management solutions to the pharmaceutical industry. However, we believe that achieving high and consistent quality is a journey that starts right from design of the plants to employee and manager training through to pre approval audits and finally certification. Thus our services cover the entire quality management life cycle.

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Projects Consultancy

We provide Pharmaceutical Projects Consultancy for Green Field and up-grade requirements of Pharmaceutical Plants for API, Bulk Drugs, Formulations, etc.

Our Plants are designed with International Regulatory requirements, cGMP, WHO, USFDA compliant and are designed as world class facilities.

Our team consists of experienced Architects and Engineers with considerable experience in Pharmaceutical & Industrial Designs.

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Welcome to CPC India Pvt. Ltd.

CPC India Private Limited is a leading provider of Quality, Regulatory and Projects Consultancy services to API, Formulations and Biotechnology companies for compliance to international regulatory requirements such as USFDA, EDQM, MHRA, TGA, MCC, WHO etc.

CPC provides Projects consultancy in design of Pharmaceutical plants as per cGMP, WHO & USFDA norms.

 

Pharmaceutical Projects Consultants

Looking for cGMP or WHO or USFDA Consultants?

If you are looking for cGMP or WHO or USFDA or International Regulatory and Projects Consultants, let us start discussing your requirements right away.