Central Drugs Standard Control Organisation (CDSCO) FDA Bhawan, New Delhi
RS Up To 3,25,000 Hyderabad, Sector 18 Chandigarh, Mohali ( Chandigarh ), South Delhi, East Delhi, Central Delhi, Roorkee, Delhi
Import & Registration Division:
•Scrutinize & examine the Drug Master Files (DMF), Plant Master File (PMF), GMP certificates & COPP etc. from overseas manufacturing units pertaining to Registration & Import License of Drugs, under Form 41, a...
Key Skills : drug regulatory affair,clinical research,epidemilogist,pharmacovigilance,technical documents
RS 2,00,000 To 3,50,000 Dehradun, Haridwar, Roorkee
Medicinal products, pharmaceuticals, veterinary medicines, medical devices, and food supplements – all these products are subject to regulations designed by governments to protect public health. The Regulatory Affairs departments of life-science co...
Key Skills : drug regulatory affair,regulatory affair,legal officer
Coordination with departments for dossier planning, preparation & approval as per Country Guidelines, Query Handling, Art Work Review, Registration process of products in new countries, Impartation of trainings ICH, CTD & ACTD Guidelines etc.
Key Skills : ctd,actd,ich,dossier,art work review,registration of products,pharmacist,pharmacy manager,pharmacy incharge,pharma associate
1. the Candidate Should Be B.pharma
2. Working Experience in Who Certified Manufacturing Unit is Must.
3. the Candidate Must have Regulatory Work Experience of Preparing
dossiers for Different Countries, Knowledge and Experience of D...