Dr. Arvind K Mishra, a global quality, regulatory and strategy expert, has over 3 decades of rich experience in Global Pharma Industry. He has obtained his Master’s Degree in Analytical Chemistry and a Doctorate in Chemistry (Pharmaceutical Drug Analysis) from Banaras Hindu University.
He has worked in well-known Indian Pharma majors like Lupin, JK Drugs and Pharmaceuticals Limited (now Teva), Strides Arcolab (now Strides Sashun Ltd), Medreich (now Meiji, Japan), Claris Injectables Ltd and Cadila Pharmaceuticals in various capacities in the areas of Quality Control, Quality Assurance, Corporate Quality Assurance, Global Regulatory Affairs, Research and Development, Clinical Research and Strategic Business Unit Head – Biologicals. He has also been actively involved in all kinds of formulations and APIs including biotech and biological, hormones, oncology (Anti-Cancer), high potent drugs, softgels, Penicillins and Cephalosporins.
Dr. Mishra is a regularly invited speaker and panelist at several Indian and overseas conferences and seminars. He has global and extensive experience in Global Regulatory requirements of US FDA, EU, MHRA, TGA, ANVISA (Brazil), MCC (South Africa), INVIMA (Colombia) and GCC (Gulf Cooperation Council countries).
Our Technical Team: We have a highly experienced 8-10 member technical team with hands-on experience and expertise in areas of QC/QA, engineering, production, project management and regulatory affairs.
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