Soul Pharma Consultancy is a professional consulting service provider specialized in providing support, guidance, and solution in formulation development, manufacturing, and regulatory.
Manoj is a multiskilled pharma professional with a dynamic career of steering organizations through developing to commercialization of complex generic products which not only include technology transfer, scale up, process optimization, regulatory compliance but also cost effectiveness.
He has thorough experience in various dosage forms including immediate and modified release tablets, capsules, tablets in capsules, liquids, suspensions, cream, ointment etc.
After completing M.Pharmacy from L.M.College of Pharmacy, Ahmedabad, he worked for Lupin Limited in multiple departments viz. manufacturing, soild dosage and injectable’s packing, process development and R&D.
When he was associated with Torrent Research Center, Gandhinagar, was mandated to create technology transfer team and the task to execute process optimization, scale up, and technology transfer of multiple own developed products for domestic, Brazil, EU and US market. Products were transferred to own as well as contract sites.
In USV, Mumbai, played instrumental role in qualification of all machines at new FDA approvable plant at Daman. Also developed products for US market and transferred for FDA filing.
In Wockhardt Limited, while heading Global Technical Services, got lifetime opportunity of transferring products from pharma companies acquired in UK and Ireland. Transferred more than 75 products in India which received regulatory approvals too. Also developed products for EU market.
In RPG Life Sciences, while heading R&D dept, apart from formulation development for domestic, Row and EU market did formulation re-engineering, cost reduction and was responsible for innovation too.
Soul Pharma Consultancy is founded by him in 2023 with a purpose to contribute in the development of pharma industry. It is a consulting firm for formulation development, scale-up, process optimization, technology transfer, bio-equivalence, dossier review, commercialization of product, resolving repeated OOS in commercial batches/trouble shooting, cost saving, optimum utilization of manufacturing facilities, site support during audit etc.
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