Ravian Life Science Pvt Ltd. has a competent Drug Regulatory Affair team which ensures
that the company complies with global regulatory requirements and enforces laws in
force from time to time.
They give strategic guidelines, right from the beginning of development of a product
(NPD), thus making an important commercial contribution in supporting the company to
produce high quality ethical products.
Our Drug Regulatory Team is capable of all type of regulatory submissions (ACTD, CTD,
eCTD) & new marketing authorizations for drug substance and drug products, product
lifecycle management including variations, Subject Matter Expertise and more.
Holistic support through various regulatory activities like DCGI/FDC filing,
Pharmacovigilance, Risk Assessment Protocol, Import/Export, Licensing, WHO-GMP filing
, Manufacturing License ( form 25 & form 28 ) , MMC , COPP , FSC , Export NOC etc.
Ravian has: –
More than 185 + COPP
More than 130 + Dossier
More than 1500 Product approval
More than 3 DCGI approval
More than 75 + FSSAI Products