Comparison of regulatory requirements for solid oral dosage forms between United States and European Union

By:

Language: English Publication details: Mysore JSSCP 2014Edition: 1Description: 140pSubject(s):

DDC classification:

Dissertation note: Balamuralidhara VJSS UniversityP.Regulatory Affairs

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	Home library	Collection	Call number	Status	Barcode
Dissertation/Thesis	JSS College of Pharmacy, Mysuru	JSS College of Pharmacy, Mysuru	Pharmaceutics	615.48 SRE (Browse shelf(Opens below))	Available	D08965

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	615.48 SIR Regulatory requirements for pharmaceutical product registration in Brunei	615.48 SOU Regulatory requisites for the registration process of biosimilar in regulated and emerging markets	615.48 SOU Asia's role in global drug development	615.48 SRE Comparison of regulatory requirements for solid oral dosage forms between United States and European Union	615.48 SRE Regulatory requirements for pharmaceutical product registration in Egypt	615.48 SRI Regulatory requirements for the approval of prescription (generics) drugs and compilation of dossier for Australia (TGA)	615.48 SRI Pharmacovigilance: How do regulatory agencies and industry work together to protect patients	Next