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 strong enough in terms of making the 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 patches and Formulation solid dossiers, capsule, injectables, spray, cream etc with 3 plant validation batches along with documentation.
would you kindly inform us that can you supply also for purchasing API/Intermediate or raw pharmaceutical materials as r&d and commercial scale?