Case analysis: Can marketing authorization can be revoked?
Yes. Marketing authorization can be revoked and it generally carried out, in case of safety issued observed with the molecule. Here is... Read More
Insight on USFDA Approves Vitrakvi® (larotrectinib), the First Ever TRK Inhibitor
Posted on29 Nov 2018
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The U.S. Food and Drug Administration (FDA) today approved Vitrakvi® (larotrectinib), the first ever oral TRK inhibitor, for the treatment of adult... Read More
Case Study: DCGI ordered the withdrawal of Voveran of Novartis
Posted on12 Jul 2018
TagsDCGI, diclofenac painkiller injection, Dynapar AQ, Product Recall, product withdrawal, themis, Transcutol-P, Voveran
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India’s drug regulator has ordered the withdrawal of the popular diclofenac painkiller injection marketed by Novartis India Ltd and made by Themis... Read More
Medical Science Liaison (MSL) – A Career Option for Healthcare Professionals !
What is The Medical Science Liaison (MSL)? The Medical Science Liaison (MSL) is a specific job related role within the healthcare industries, e.g.... Read More
NCK Pharma to introduce new edged “EMOTION BASED LEARNING” in the field of Pharmaceutical Learning
Bangalore (India), Press Release — NCK Pharma Solution Private Limited (popularly know as NCK), leading diversified training provider in the filed of... Read More
What is difference between phase IIa and Phase IIb clinical trial?
Posted on24 Jul 2016
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Phase II studies are sometimes divided into Phase IIA and Phase IIB. Phase IIA is specifically designed to assess dosing requirements (how... Read More
Basic Pharmacovigilance Competency Test
Abbreviated as PV or PhV, Pharmacovigilance is the science relating to the detection, assessment, understanding and prevention of adverse effects, particularly long term and short term side... Read More
FDA approves first-of-its-kind corneal implant
The U.S. Food and Drug Administration today approved the KAMRA inlay, a device implanted in the cornea of one eye (the clear,... Read More
10 New Molecular Entity approved by USFDA in 2015 till date
As on that 10 new molecular entity is approved by USFDA. No. Drug Active Ingredient FDA-approved use on approval date 10 Cholbam... Read More
FDA Launches Drug Shortages Mobile App
U.S. Food and Drug Administration launched the agency’s first mobile application (app) specifically designed to speed public access to valuable information about drug... Read More