India has the potential to increase global clinical trials in the country by five times in the coming years, a report has said, with experts highlighting the significant opportunities for biopharma companies to leverage India's rich diversity and robust healthcare infrastructure to develop innovative treatments. The joint report by the USA India Chamber of Commerce & PwC India titled, Clinical Trial opportunities in India which will be released at the virtual edition of the 17th annual BioPharma & Healthcare Summit 2023 to be held on Wednesday in Boston also indicates that through several key drivers, India is emerging as a favourable destination to conduct clinical trials. According to the report, the private sector is a well-suited channel for the top biopharma to conduct more efficient clinical trials with easier and faster access to investigators and patients. According to the report, India has the potential to increase global clinical trials in the country by five times ..
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Mansukh Mandaviya, Union health minister, said that the policy has been designed keeping in mind the need to have a holistic policy framework and will accelerate the growth of this sector
Thyronorm has no quality issue, mislabeled batch was invoiced in Madhya Pradesh and Telangana: Company
The World Health Organisation has issued a 'WHO Medical Product Alert' after "Substandard (contaminated)" Guaifenesin Syrup TG Syrup was found in the Marshall Islands and Micronesia
The Rs 4,326-crore public issue's price band is set in the range of Rs 1,026-1,080 per share. The issue will close on Thursday, April 27
Hospitals to recover from sluggish Q3; diagnostics growth rate at pre-Covid levels
Hospitals to recover from sluggish Q3; diagnostics' growth rate at pre-Covid levels
The NITI Aayog has recommended that Indian standards of drug regulation should be on par with global standards as well as aligned with the International Council for Harmonisation guidelines while promoting ease of doing business. The apex public policy think tank of the central government also suggested creating a separate authority to regulate medical devices in the country which is currently being monitored by the Drugs Controller General of India (DCGI). The recommendations have been made during the ongoing inter ministerial consultation on the New Drugs, Medical Devices and Cosmetics Bill, 2023. The draft New Drugs, Medical Devices and Cosmetics Bill, 2023, which seeks to replace the existing Drugs and Cosmetics Act of 1940, was put up on public domain in July last year seeking feedback from stakeholders. It has been revised and sent for inter-ministerial consultation. On clinical trials, the NITI Aayog said the draft bill should reflect the intent of overcoming the hesitancy
The latest drug recalls just add to a long line of scandals that have tainted the pharma sector of India
Pharma shares like Aurobindo Pharma, Zydus Lifesciences, Sun Pharmaceutical Industries Ltd, Glenmark Pharmaceuticals may rise up to 14 per cent.
Earlier this month, the company had incorporated a wholly-owned subsidiary, Morepen RX.
In the near term, higher R&D costs and a recent acquisition to weigh on earnings growth
New launches in the US, market share gains and steady domestic growth are positives
Surge in demand for Covishield led to a huge spike in its revenues and profits
System will bring together stakeholders like manufacturers, distributors, state-run agencies to ensure quality
The state government participated in the country's largest pharma expo to showcase the pharma ecosystem and invite potential medical devices players for investments
Analysts believe that some of the recent observations from the US FDA are critical in nature and could lead to a potential Official Action Indicated (OAI) classification for the Indore plant
Proposals to be discussed at Hyderabad conclave include having a centralised drug registration system under CDSCO
Appointment comes at a time when India's pharma regulatory landscape is under the scanner