DeveshDRA

64 Followers

fda pharmaceutical industry pmda mhlw pal regulatory affairs medical device approval in japan pharmaceuticals change management change control pharmaceutical regulatory barcode

Activity
About

Comparative Study of Dossier Compilation & Submission Process of Drug Product in USA, Europe & India.

12 years ago • 19770 Views

Validation of cms used for compliance with regulatory requirements in pharma industries

12 years ago • 1264 Views

Regulatory aspect of barcode technology

12 years ago • 4325 Views

Regulatory aspect of pharmaceutical change control system

12 years ago • 45540 Views

MEDICAL DEVICE APPROVAL PROCESS IN JAPAN

12 years ago • 6112 Views

Antidepressants

Bhudev Global • 7 years ago

Drug Master Files under GDUFA

GMP EDUCATION : Not for Profit Organization • 11 years ago

Preparing Compliant eCTD Submissions

Scott Abel • 15 years ago

eCTD Submissions

Quintiles, Mumbai, India • 14 years ago

The Electronic Regulatory Submission

Dr.RAJEEV KASHYAP • 14 years ago

Visual and Creative Thinking:What We Learned From Peter Pan and Willy Wonka

Kelsey Ruger • 16 years ago