cGMP Representative Consultant

Our extensive experience in pharmaceutical and medical device industries will ensure that critical compliance issues are on the project plan.

Toxicological Reports

More than 1,900 PDE / ADE reports

Toxicological Evaluation of Impurities and Risk Analysis

Toxicological issues are key in the pharmaceutical industry due to the need to comply with current regulations.

British Retail Consortium - BRC

Your Organization can Access those Parts of the Market that are Only Available to those that are Certified

Lifecycle Approach of Process Validation

Support You on Your Validation Journey

Preparation of Pharmacovigilance Master File.

System Evaluation and Technical Comparison

Evaluate and Choose the comply and cost-effective system

Thermal Mapping and Qualification Studies

Thermal Mapping as per the Latest Guidelines and Requirements