Biophore India Pharmaceuticals Pvt. Ltd.
Geetha Senchani is a pharmaceutical professional with extensive experience in drug development and intellectual property management. Currently serving as General Manager at Biophore India Pharmaceuticals Pvt. Ltd. since July 2018, Geetha previously held the position of AGM-Portfolio at Hetero Drugs Ltd. from February 2015 to June 2018, where responsibilities included analyzing market opportunities for generic drugs and supporting long-term pipeline planning. From June 2005 to January 2015, Geetha worked as Senior Manager IPM at Aurobindo Pharma, focusing on patent evaluation, freedom to operate analysis, and assisting in various aspects of patent applications and marketing support. Geetha holds an M.Pharm degree from the Birla Institute of Technology and Science, Pilani, obtained between 2002 and 2004.
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Biophore India Pharmaceuticals Pvt. Ltd.
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Biophore is a research driven global pharmaceutical company focused on development, manufacturing and marketing of Active Pharmaceutical Ingredients (APIs) having its operations based in Hyderabad, India and also has a registered office in New Jersey, USA. Biophore has two dedicated R&D facilities in Hyderabad and Vishakapatnam. The research facilities are fully equipped with wide range of R&D and process equipment from USA with reaction capabilities from milligram to kilogram. Ever since its establishment in 2007, Biophore recognized that there were two ways of growing the API business: manufacture a large API product basket, or pick a handful of promising APIs in select therapeutic categories and grow them over the long-term. Biophore consciously chose the latter option and focused on not only building competencies and adding scale in those segments but more importantly, building efficiencies that would make it an undisputed leader in these products of choice. The product range is constantly expanded through its own R&D, process development, technology transfers, joint ventures and collaborations. Biophore’s core strength lies in development of non – infringing routes for comprehensive range of bulk actives and intermediates, development of niche APIs, oncology APIs, APIs for MRI contrast agents and APIs for NCE - 1 filing. Biophore has made strategic investments in two manufacturing facilities. Sionc pharmaceuticals & Azico – Biophore, Both located at Vishakapatnam. Among them Sionc, a multi-purpose plant has passed FDA inspection in 2013 & 2016 with no observations on the Form 483. This is the reason to be proud and confirmation of the highest quality standards of Biophore. Our other facility Azico – Biophore is also a n FDA approved facility that strictly complies with cGMP procedures and maintains well documented SOPs, with a modern quality control laboratory thereby ensuring the production of highest quality APIs.