A well-designed Quality Management System (QMS) blends regulatory and practical aspects. In addition to continuous improvement, periodic audits & training, QA team ensures comprehensive, adequate and effective implementation of the QMS.
Design & maintain a code of standard for quality that meets regulatory and business requirements.
New employee orientation and Periodic re-enforcement trainings to ensure consistent execution.
Ensuring all departmental operations are carried out as per QMS.
Processes & tools for managing planned and unplanned deviations.
Remediation of quality incidents with appropriate resolution for uninterrupted operations.
Proactive action to prevent the occurrence of quality issues and measuring their effectiveness.
Annual product quality reviews for continuous improvement and effectiveness of QMS.
Soliciting and incorporating user feedback into the QMS for continuous improvement and adoption.
Managing market complaints with due attention and care so that patients get superior quality medicines.
From raw material induction to in-process testing to finished product testing, Quality Control department plays an important role at every stage of the product life cycle. The identity, purity, stability and potency of the products is established and ensured through rigorous adherence to predetermined specifications of globally approved Pharmacopeia (USP, BP and IP).
Conducting physical, chemical and microbial tests on materials and products
Issue Certificate of Analysis (CoA)"
Maintain equipment and resources in validated/qualified status