S.M. Mudda Email & Phone Number

• A Pharmacy graduate with Post Graduate Diploma in Management studies. 43 years experience in India covering all aspects - Technical, Quality Systems, Regulatory Affairs, Project Management , Training and Education , Leadership Development and Business Management. • Passionate about implementation of best-practice Pharmaceutical Quality System (PQS) for implement ion of GMPs and for creating a culture of quality across the organisation.. Managing Director of Misom Labs Limited, Malta, EU GMP Certified, state-of-the-art, Pharmaceutical Testing Laboratory. Misom Labs offers EU importation, Testing and Batch Release ( QP Release) and GMP Audit Services. • Was associated with Micro Labs Limited , Bangalore for the last 33 years and held several key positions -Executive Director ,Technical & Operations and as Director, Global Strategy - Technical.• As a Program Director, Designed MBA-Style, Advanced Program in Pharmaceutical Quality Management (APPQM), for IDMA in collaboration with NSF, UK. Successfully completed the First Batch consisting of 40 Delegates from across the Pharma Industry. • Designed World-Class GMP-Compliant facilities for manufacture of various Dosage Forms including OSDs, Sterile Products, Ophthalmics in Blow-Fill-Seal packs.• Regular Speaker, Panelist, Moderator at various national and international forums on wide range of topics- Pharmaceutical Quality System, Culture of Quality, Data Integrity.• Engaged with Government and Regulators for policy matters related to pharmaceutical industry as Chairman , Regulatory Affairs Committee, of IDMA , Mumbai.• Ex-Member of Scientific Body, Indian Pharmacopoeia commission, Ghaziabad , engaged in development of monographs for Ophthalmics. • Former Board Member , Committee of Administration, Pharmaceutical Exports Promotion Council ( Pharmexcil), Ministry of Commerce & Industry, Government of India• Former Director , ISPE India Affiliate, a professional US - based professional association

Listed skills include English, 1. Facility Design, 21 Cfr Part 11, 3. Quality Management System, and 24 others.