Personal Information
Entreprise/Lieu de travail
Mumbai Area, India India
Profession
Senior Executive Regulatory Affairs at Cipla Limited
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
NA
À propos
-Young master candidate in pharmaceutical management having more than 6 years of experience in pharmaceutical drug regulatory affairs (formulation), formulation development & site transfers and more than 1 year of experience in regulatory affairs project management.
-Experience in planning of projects, execution, monitoring & controlling and closure of the projects.
-Adept in managing new applications, response to queries, post-approval changes and renewals of the drug products.
-Adept in communicating with health authorities, consultants and vendors.
-Regulatory assistance to the scientists during drug product development stages.
-Experience in eCTD and NeeS submissions through RAMA...
Mots-clés
innovator selection
reference medicinal product
drug regulatory affairs by mr. pankaj dhapade
regulatory aspects on pharmaceutical excipients by
Tout plus
Présentations
(3)J’aime
(1)Regulatory Aspects On Pharmaceutical Excipients By Mr. Pankaj Dhapade
Pankaj Dhapade
•
il y a 10 ans
Personal Information
Entreprise/Lieu de travail
Mumbai Area, India India
Profession
Senior Executive Regulatory Affairs at Cipla Limited
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
NA
À propos
-Young master candidate in pharmaceutical management having more than 6 years of experience in pharmaceutical drug regulatory affairs (formulation), formulation development & site transfers and more than 1 year of experience in regulatory affairs project management.
-Experience in planning of projects, execution, monitoring & controlling and closure of the projects.
-Adept in managing new applications, response to queries, post-approval changes and renewals of the drug products.
-Adept in communicating with health authorities, consultants and vendors.
-Regulatory assistance to the scientists during drug product development stages.
-Experience in eCTD and NeeS submissions through RAMA...
Mots-clés
innovator selection
reference medicinal product
drug regulatory affairs by mr. pankaj dhapade
regulatory aspects on pharmaceutical excipients by
Tout plus