Mondaq India: Food, Drugs, Healthcare, Life Sciences
Singh & Associates
On January 12, 2018, the European Medicines Agency's Pharmacovigilance Risk Assessment Committee recommended the suspension of the marketing authorizations for hydroxyethyl-starch solutions for infusion across the European Union.
Singh & Associates
On January 23, 2018, the European Medicines Agency (EMA) has published its annual report titled ‘Human medicines: Highlights of 201741.
Singh & Associates
Haemophilia A is an inherited bleeding disorder caused by lack of a clotting protein called factor VIII and mainly affects males.
Singh & Associates
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 6-9 November 2017 ...
Singh & Associates
On January 03, 2018, Novartis announced that KisqaliR (Ribociclib) has received FDA Breakthrough Therapy designation for initial endocrine-based treatment, in combination with tamoxifen or an aromatase inhibitor,...
Singh & Associates
On January 15, 2018, the World Health Organization's (WHO) Global Tuberculosis Programme has released a Position Statement on the use of delamanid in treatment of multidrug-resistant tuberculosis (MDR-TB).
Singh & Associates
On January 29, 2018 World Health Organization (WHO) released the surveillance data of new "Global Antimicrobial Surveillance System (GLASS)" on antibiotic resistance.
Singh & Associates
The National Pharmaceutical Pricing Authority, is an executive body under the Drugs (Prices Control) Order, 2013 under the Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Government of India.
Singh & Associates
The United States Food and Drug Administration (USFDA) approved more Abbreviated New Drug Application (ANDA) in 2017 than any other year, according to its latest FY 2017 activities report.
Singh & Associates
On January 19, 2018, the CDSCO has published clarification regarding issuance of NOC for issuing Form 29 License used to manufacture drugs for the purposes of examination, test or analysis of biological products (Vaccines 86 r-DNA products).
Khaitan & Co
The DTAB has reportedly appointed an expert committee under Ms Nilima Shirsagar, retired dean of Mumbai's KEM Hospital to review the safety, efficacy and therapeutic justification of several fixed dose combinations.
Singh & Associates
Shortly after SAGE's recommendation, Gavi Board approved US$85 million in funding for TCVs starting in 2019.
Singh & Associates
The Union Budget 2018 was presented by Finance Minister (FM) Arun Jaitey on February 01, 2018.
Singh & Associates
The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for discharging functions assigned to the Central Government under the Drugs and Cosmetics Act, 1940 and Rules, 1945.
Singh & Associates
An estimated 1-in-10 medical products circulating in low- and middle-income countries is either substandard or falsified, according to new research from WHO.
Singh & Associates
The World Health Organization (WHO) organized the WHO Global Ministerial Conference in Moscow, Russia from 16-17, November 2017. The conference was attended by more than 1000 participants including Ministers ...
Singh & Associates
The Indian Pharmacopoeia Commission (IPC) has released the Eighth Edition of Indian Pharmacopoeia (IP-2018). It was released by the Secretary, Ministry of Health & Family Welfare, Government of India.
Singh & Associates
The Ministry of Health & Family Welfare has recently announced the launch of daily regimen for TB patients across the country, under the Revised National TB Control Programme (RNTCP).
Singh & Associates
On November 23, 2017, National Pharmaceutical Pricing Authority (NPPA) has fixed/revised the retail price/ceiling price of 51 formulations of schedule-I formulations under Drug Price Control Order (DPCO), 2013.
Singh & Associates
On December 13, 2017, the World Bank and World Health Organization (WHO) released the Universal Health Coverage (UHC): 2017 Global Monitoring Report; simultaneously published in Lancet Global Health ...
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Singh & Associates
In the words of advertising tycoon Leo Burnett, "Let's gear our advertising to sell goods but let's recognize also that advertising has a broad social responsibility."
Kochhar & Co.
The Legal Metrology (Packaged Commodities) Rules, 2011 ("Packaging Rules") regulate pre-packaged commodities in India and inter – alia mandate certain labeling requirements prior to sale of such commodities.
Singh & Associates
The World Health Organization (WHO) organized the WHO Global Ministerial Conference in Moscow, Russia from 16-17, November 2017. The conference was attended by more than 1000 participants including Ministers ...
Singh & Associates
The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for discharging functions assigned to the Central Government under the Drugs and Cosmetics Act, 1940 and Rules, 1945.
Khaitan & Co
The purpose of the Legal Metrology (Packaged Commodities) Rules, 2011 (PCR) is to regulate pre-packaged commodities. Under the PCR, pre-packaged commodities must comply with certain mandatory labelling requirements.
Singh & Associates
The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for discharging functions assigned to the Central Government under the Drugs and Cosmetics Act.
Singh & Associates
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 6-9 November 2017 ...
Singh & Associates
On December 13, 2017, the World Bank and World Health Organization (WHO) released the Universal Health Coverage (UHC): 2017 Global Monitoring Report; simultaneously published in Lancet Global Health ...
Singh & Associates
Dengue is a mosquito-borne viral infection causing a severe flu-like illness and, sometimes causing a potentially lethal complication called severe dengue.
Singh & Associates
On November 23, 2017, National Pharmaceutical Pricing Authority (NPPA) has fixed/revised the retail price/ceiling price of 51 formulations of schedule-I formulations under Drug Price Control Order (DPCO), 2013.
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