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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

ISO 31000:2018 - Risk Management

Achieve an Effective Risk Management System

ISO 22000:2018 - Food Safety Management Systems

Achieve an Effective Food Safety Management Systems

ISO 14001:2015 - Environmental Management Systems

Achieve an Effective Environmental Management Systems

ISO 13485:2016 - QMS for Medical Devices

Achieve an Effective Quality Management Systems for Medical devices