Training on Data Integrity and Good Documentation Practices & How to Face Regulatory Inspections
Compliance to current Good Manufacturing Practices (cGMP) is essential not merely to ensure consistency in the practices in getting the productive outcome, but also helps business to sustain in the regulatory environment through building a trustworthy relationship with all stakeholders including regulators and customers. A culture of quality is the critical element that brings all teams together to develop and sustain continual quality improvement with compliance to GMP and ensures that the quality system and its sub-systems (production system, Facility & equipment system, Laboratory control system, and warehousing system) functions in full integration and maintaining a state of control across the process life cycle.
CGMP helps to ensure proper design, monitoring, control, and sustaining of the manufacturing Processes and facilities through implementing practical procedures to meet High-quality standard products –Active or Drug Intermediates. Embedding Data integrity (DI) and Good Documentation Practices (GDP) within cGMP reaffirm the regulatory compliance industry's commitment to manufacturing safe, quality products that fulfills the intended requirements.
In line with the goal outlined above and to enhance a culture of quality at our internal site, Sanjeev Kumar, Head of Quality & Regulatory Affairs, has imparted multiple training sessions on "How to Face Regulatory Inspections & Data Integrity with Good Documentation Practices" in Aug-23 to cover more than 100 colleagues at Jubilant Ingrevia Limited-Bharuch Learning centre.
