Dr. Tarun Chugh has rich 30+ years of experience in Leading MNC, Indian and Middle East Co. for Quality Assurance / Control / Quality Management System / Handling Audits / Market Complaints. Vast involvement in development of Quality Systems / Quality culture of leading companies in Indian and Global MNCs for global market including USA, UK, Australia, Brazil, African Market and Canada. He has done many Audits for USFDA / MHRA / ANVISA / Canada and other EU/ ROW markets customers and third audits for multi-locations. He has Good exposure for Data Integrity handling as per Part 211 CFR Part 11 /GxP_PIC/s
He is passionate about training and coaching people working in pharma industry in classroom and on webinar for distance location learners. Good experience for harmonization of the systems, policies, process, and work culture across various plants by standardization e.g. Quality Policy / VMP / SMF / Protocols / SOPs and documentation chronicle as per 4 level Data pyramid.
He has Good understanding of Aseptic / Terminal Sterilization tech. and microbiology requirements for clean area with non-viable / viable controls, Media fill / Smoke test (for DP and air flow patterns)/ Water generation and distribution system and its validation. Trouble shooting for pharmaceutical dosage forms (Injectable/Tablet / Capsule / Liq. / Ointment), also has sound knowledge of Validations and validation audits / documentation review.
3-Hour Virtual Seminar On How To Prepare An Effective SOP – Workshop With Case Study