We are a group of Quality practitioner`s with over 25 years of experience in the field of Analytical Development, Pharmaceutical regulations and Audit Compliance.
Our team is competent to deal with Analytical developments, Quality Systems (QA/QC) for both Active Pharmaceutical Ingredients (API) and Finished Products (FP). We ensure that our activities are aligned with the regulatory requirements like cGMP, ICH Q11, M7, etc.
