Indian Drug Manufacturers’ Association (IDMA) and IDMA Technical Subcommittee will organise a seminar on Managing Risks for Quality Compliance 2014 on May 16, 2014 in Mumbai. Experts in technology,quality assurance,regulatory affairs,engineering,production,and packaging spheres from the Indian pharmaceutical industry will converge and interact on various recent developments.
Dr K Bangarurajan, Deputy Drugs Controller (India),CDSCO West Zone (Mumbai) will give the keynote address on ‘QRM Requirements of WHO’; Bharat Doshi, Pharmaceutical Consultant, will peak on ‘Risk Free Facility Design for efficient QRM’; SM Mudda, Executive Director,Technical & Operations- Micro Labs will speak on Managing Operational Risks for Quality Products; R Raghunandanan, Pharmaceutical Consultant, will speak about ‘Managing Risks in Quality of Aseptic Operations’; R R Tuljapurkar, Vice President,Quality Assurance, Zydus Cadila, will speak on ‘Controlling Risks in Quality Control’; R Dadich, Vice President,Corporate Quality,IPCA Laboratories will speak on ‘Quality Materials for Quality Products-Controlling Risks.’
The seminar is designed to cater to all those involved in pharmaceutical industry, bio-pharmaceutical industry, academic institutions; business consulting companies, facility design and materials management.
EP News Bureau – Mumbai
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