Normal view MARC view ISBD view

Post Approval Regulatory Compliance Management for Generics in U.S. Market

By:

Material type: Text

TextPublication details: Ahmedabad Institute of Pharmacy, Nirma University 2016Description: 85pDDC classification:

Online resources:

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

Holdings
Item type	Current library	Collection	Call number	Status	Notes	Date due	Barcode	Item holds
Dissertation	NIMA Knowledge Centre Reference	Reference	615.1901 DOS (Browse shelf(Opens below))	Not For Loan			PDR00387
CD/DVD	NIMA Knowledge Centre Reference	Reference	615.1901 DOS (Browse shelf(Opens below))	Not For Loan	Dissertation CD		PDR00387-1

Total holds: 0

Previous	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	Next
Previous	615.1901 DOC RP-HPLC Method for Estimation of Tiapride Related Subtance in Tablet Formulation	615.1901 DOC RP-HPLC Method for Estimation of Tiapride Related Subtance in Tablet Formulation	615.1901 DOS Post Approval Regulatory Compliance Management for Generics in U.S. Market	615.1901 DOS Post Approval Regulatory Compliance Management for Generics in U.S. Market	615.1901 DOS Overview of Stability Studies	615.1901 DOS Regulatory requirements and Current Challeges related to Related to Labling and Packaging for Medicinal Products in Europe Region	615.1901 DOS Regulatory requirements and Current Challeges related to Related to Labling and Packaging for Medicinal Products in Europe Region	Next

Guided by Dr. Priti J. Mehta and Mr. Vikas Johri

There are no comments on this title.

to post a comment.