COMMON DEFICIENCIES RAISED BY VARIOUS REGULATORY AGENCIES
Journal Title: International Journal of Drug Regulatory Affairs - Year 2014, Vol 2, Issue 2
Abstract
Timely Product registration is a challenge in today’s scenario. Regulatory agencies are keen in assessing CTD sections like redefining starting material of Drug substance manufacturing, Pharmaceutical development, impurities in Drug substance and Drug product, Container-closure. Common deficiencies are presented in this article.
Authors and Affiliations
Mohidekar S, Maharao V, Badjatya J. K.
HARMONIZATION & ADVANCEMENT IN PHARMACEUTICAL INDUSTRY
The urgent requirement to rationalize and harmonize regulation was impelled by instance of rising cost of Health care, Research and Development and need to meet the public requirement to approach for the safe and efficac...
COMMON DEFICIENCIES RAISED BY VARIOUS REGULATORY AGENCIES
Timely Product registration is a challenge in today’s scenario. Regulatory agencies are keen in assessing CTD sections like redefining starting material of Drug substance manufacturing, Pharmaceutical development, impuri...
NUTRACEUTICALS - A REGULATORY REVIEW
The Nutraceuticals are the emerging sector in the Pharma Industry. As people are more and more concerned about their health and diseases caused by the malnutrition, the growth of the Nutraceuticals worldwide are inevitab...
FORMULATION AND IN VITRO EVALUATION OF EXTENDED RELEASE MATRIX TABLETS OF LEVOSULPIRIDE BY USING NATURAL POLYMERS
The aim of the present study was to develop sustained release formulation of Levosulpiride to maintain constant therapeutic levels of the drug for over 12 hrs. By using various Natural polymers like Fenugreek, Almond gum...
DRUG REGULATORY PROCEDURES IN TANZANIA: A GLIMPSE
In Tanzania, Tanzania Food and Drugs Authority (TFDA), is a regulatory body responsible for controlling the quality, safety and effectiveness of food, drugs, herbal drugs, cosmetics and medical devices. The Authority has...