Hostrin Life Sciences

We are a global pharmaceutical regulatory techno commercial consultancy services. We assist pharmaceutical and life sciences industries for both human and veterinary to register their products and access the rapidly growing diverse markets throughout the world. We provide regulatory services for dossier submissions such as DMF / CTDs-ACTD / ANDA / Validations / cGMP / GLP / PSUR / BA-BE Studies. We have been assisting regulatory services for pharmaceutical and life sciences industries for different countries like US, Europe Region and ROW countries like Australia, New Zealand and Asia – Singapore, Malaysia, Indonesia, Thailand, The Philippines, Vietnam, Iran, Egypt, Israel, African Countries, Russia, Taiwan, Hong Kong, South Korea. We are capable to guide for the making of documentations like Tech pack, DMF’s for API’s and CTD’s/ACTD’s, eCTD’s, ANDA’s for Formulations and combinations with Tech Transfer for API’s, Biotechnology, Bio similar products, Transdermal and Formulation solid dossiers, capsule, injectables, spray, cream etc with 3 plant validation batches along with documentation. Our mission is to inspire the organizations to work more efficiently and create greater choice in the domain of Regulatory services for the benefit of all of our associates. To be a India’s best provider for the Regulatory solutions –A business that has a positive impact on millions of people every day, we are conscious for our Global role in the Corporate Pharma World.