An investment share above 30 per cent is considered important for driving economic growth
The WHO-led experts team approved India's vaccine regulatory system after an in-depth scientific review, conducted between September 16 and 20, as per a statement by the Ministry of Health and Family
The new guidelines have been formulated by India's drug regulatory body to ensure product traceability, which has been hindered by insufficient documentation throughout the distribution network
sickle cell disease is a genetic blood disorder that causes severe pain and complications. It is particularly prevalent among tribal populations in India
An advisory issued by the DCGI to all states and Union Territories, read that "blood is not for sale", it's only for supply and that only processing costs may be charged by the blood centres
Renal cell carcinoma (RCC), the most common type of kidney cancer, predominantly affects men and has limited treatment options, often leaving patients at risk of recurrence
Only 2,000 of the 10,500 manufacturing units in the country have the World Health Organization's GMP certification
Akums Drugs and Pharmaceuticals on Thursday said it has received approval from the Drug Controller General of India (DCGI) for triple combination diabetes medication. Sitagliptin 100, Pioglitazone 15 and Metformin 1000/500 have been combined for the treatment of diabetes and offers a number of pharmacological advantages, the company said in a statement. The combination drug is going to better serve anti-diabetic patients, who require better treatment without necessarily swallowing multiple drugs. Akums Drugs & Pharmaceuticals Joint Managing Director Sandeep Jain noted that the renoprotective effects of drugs like metformin, coupled with the functional and corrective influence of pioglitazone on beta-cell and metabolic syndrome and the stability of Sitagliptin, make an effective solution for diabetes. "As a brand, we will continue to introduce new combinations to help patients around the world get better," he added.
India's drug regulator DCGI has written to drug controllers of all states and Union territories and the Pharmacy Council of India asking them to ensure that pharmacists are physically present in retail medical stores and that medicines are sold under their direct supervision. In a letter, Drugs Controller General of India (DCGI) Dr Rajeev Singh Raghuvanshi sought strict implementation of section 42 (a) of the Pharmacy Act 1947 and Rules 65 of the Drugs and Cosmetics Act 1945 in retail pharmacies. Ensure that pharmacists are physically present in the retail pharmacies/medical stores, and that medicines are sold/dispensed under their direct supervision. Ensure that no prescription medicine is sold/dispensed from the retail medicines shop without a proper and valid prescription," the DCGI said in the letter sent on March 9. The drug regulator referred to a letter from Suresh Khanna, National General Secretary, IPA, Mumbai which highlighted issues pertaining to implementation of Section
Drug firm AstraZeneca India on Friday said it has received approval from the domestic drug regulator to market a drug to treat biliary tract cancer (BTC) in the country. The company has received approval from the Central Drugs Standard Control Organisation (CDSCO) for Durvalumab, the drug firm said in a statement. BTC is a group of rare and aggressive gastrointestinal (GI) cancers that form in the cells of the bile ducts (cholangiocarcinoma), gallbladder or ampulla of Vater (where the bile duct and pancreatic duct connect to the small intestine). Apart from ampullary cancer, early-stage BTC often presents without clear symptoms and most new cases of BTC are therefore diagnosed at an advanced stage, when treatment options are limited, and the prognosis is poor. More than 30,000 new cases of BTC are seen in India every year with 90 per cent of them diagnosed in the advanced stage. "The approval underpins our commitment to transform patient outcomes by harnessing the power of science
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Gives firms two days to respond to allegations that they flouted rules
The first nine patients that they will inject would be legally blind, as they have to prove safety first
The tenure of Dr V G Somani as the Drugs Controller General of India (DCGI) has been again extended by another three months, according to an order issued by the Union Health Ministry. The extension will come into effect from Tuesday, the order said. He was earlier given an extension in August this year. "In continuation to office order dated 16.08.2022, the competent authority has concurred approval for Dr V G Somani, to continue to hold the charge of the post of Drugs Controller of (India) for a further period of three months w.e.f. 16.11.2022 or until further order, whichever is earlier," it said. Dr Somani was appointed the DCGI for a term of three years on August 14, 2019. The DCGI heads the Central Drugs Standard Control Organisation (CDSCO), which is responsible for ensuring quality drugs supply across the country.It also has authority to give approval to new drugs and regulate clinical trials.
India had the highest number of participating companies after the host, UAE, at the four-day event
Bharat Biotech's iNCOVACC cleared for 2-dose regimen
Gennova Biopharmaceuticals Ltd aims to produce around 4 - 5 million doses per month and this capacity can be quickly doubled
It is for the first time ever that Covid-19 vaccine remains stable during storage even at 2-8 degrees Celsius
The CBI team, after getting inputs about exchange of bribery, allegedly carried out trap operation in which some persons were apprehended, officials said.
April saw revenue surplus of Rs 591 crore