Editorial
 SLOW PROGRESS ON IPDMS   
 Wednesday, September 20, 2017 
 National Pharmaceutical Pricing Authority had set up an Ingredient Pharmaceutical Database Management System (IPDMS) in the country in September 2014 aimed at facilitating online submission of mandatory cost data by all pharmaceutical companies in the country. 
  Past Editorial...  
TODAY'S NEWS
13:00  [IST]Innovaccer introduces disruptive Care Intelligence System
12:00  [IST]Sancilio Pharma's Altemia receives US FDA rare pediatric disease status for treatment of SCDi n children
11:00  [IST]Arkis BioSciences' CerebroFlo EVD catheter with Endexo technology receives US FDA approval
10:00  [IST]Absorption Systems ink research pact with US FDA to share data on modeling & simulation to improve development of veterinary, human drugs
09:00  [IST]WHO report shows world is running out of antibiotics
more news >>
TOP NEWS
08:00  [IST]DoP asks NPPA to re-fix ceiling price of Co-Trimoxazole tablet after examining documentary proof submitted by Cadila Healthcare
08:00  [IST]MCI set to issue guidelines on peer group evaluation of professional incompetence of medical practitioners
08:00  [IST]Health ministry directs faculties in 35 institutes to guide studies for intensive ADR monitoring exercise under PvPI
08:00  [IST]Karnataka govt' thrust on ethical medical service to ensure transparency across private & govt hospitals
08:00  [IST]IPC to hold workshop on 'Establishment of PV System in Pharma Industries" on Oct 12 at SciTech Centre, Mumbai
08:00  [IST]DBT to conduct 'India-UK antimicrobial resistance sandpit' to address the challenge of antimicrobial resistance in India
more news >>
YESTERDAY'S NEWS
18:00  [IST]Study shows exposure to pet and pest allergens during infancy linked to reduced asthma risk
17:00  [IST]Novartis' Rydapt gets EU approval for newly diagnosed FLT3-mutated acute AML & 3 types of advanced SM
16:00  [IST]Russia and India embark on transfer of technologies of drugs production for treatment of HIV infection
15:00  [IST]Inovio, Partners begin phase 1/2a trial to advance its vaccine against deadly MERS infection
14:15  [IST]Strides Shasun receives US FDA approval for generic Lovaza
14:00  [IST]Pfizer announces outcome of FDA committee meeting for Sutent in patients at high risk of recurrent RCC after surgery
more news >>
INTERVIEW  
FDA action plan to beef up drug regulatory system
Maharashtra FDA Commissioner, Dr Pallavi Darade
Past Interviews...
 
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