Principal Consultant

Vasundhara has over 29 years of leadership and diversified experience in the pharmaceutical industry and associated with Audit Docs for over 3 years as a principal consultant.

Vasundhara previously worked as a Quality Head in GSK India Pharmaceuticals Limited and AstraZeneca, India. She is an IRCA certified lead auditor and performed more than 250 GMP/GDP/GLP and Gap assessment audits for various companies across the world and delivered more than 100 training programs.

At Audit Docs, Vasundhara guides and provides expertise to handle quality solutions to address complex regulatory, compliance and quality challenges.

Consultant

Hitendra is a quality-oriented professional with over 23 years of experience in quality assurance, quality control, quality engineering, audits and compliance functions.

Hitendra executed more than 500 GMP/GLP/GAP audits and trained more than 1000 professionals. He successfully designed, implemented and provided support in achieving US FDA and EU GMP certification for multiple API and FDF companies. He is a CQI-IRCA certified lead auditor and previously worked in MNCs like Sun Pharma, USV, AstraZeneca, Mylan, Sanofi, Zydus Cadila and Alembic.

At Audit Docs, Hitendra involves in providing business solutions in Pharmaceuticals in the arena of Compliance, Regulatory and Project Management.

Consultant

Srini is certified by CQI-IRCA, APIC, and ECA and lead auditor for ISO 9001, 14001 and 45001 standards. He performed more than 400 GMP/GDP/GLP/Gap Assessment Audits and executed 15+ GMP assignments across the world.

Consultant

Durga is our consultant and executes GMP/GLP/GDP audits on behalf of Audit Docs across India and Asian countries. He has over 16 years of experience in quality assurance, audit and compliance functions.

He is a CQI-IRCA certified lead auditor and executed over 150 audits in his career.

Manager – Operations

Ramya is our operations manager and is part of the management team. She oversees high-level activities at Audit Docs, analyses and improves organizational processes, and works to improve the quality, productivity, and efficiency of our services.

Principal Consultant

Saravana is a seasoned pharmaceutical professional with over 22 years of experience across the pharmaceutical industry. He successfully handled more than 20 regulatory inspections and performed more than 150 GxP audits for FDF and API facilities. He has strong exposure to quality, regulatory, commissioning, qualification and validation of green field projects. He is a key note speaker and trainer and delivers onsite training programs.

At Audit Docs, Saravana provides consulting services to address quality challenges and ensures the end-to-end compliance progress of the facility.