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