USFDA authorises first tests that estimate patient’s antibodies from past SARS-CoV-2 infection
Cautions patients against using the results from any serology test to stop social distancing, discontinuing wearing masks or…
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US FDA sets new template for non-lab COVID-19 diagnostic test developers
New recommendations aim to help get tests to market that are simple enough to use at home, similar to a pregnancy test
COVID-19: Import licenses for rapid diagnostic kits of three firms cancelled, 16 suspended by DCGI
The three firms are Cadila Healthcare, MDAAC International and N W Overseas, while the 16 companies include Transasia…
Phase 3 COVID 19 clinical trials to be designed with stringent success criteria: International…
The meeting participants stressed the need for large phase 3 clinical trials that enroll many thousands of people, including those…
US FDA approves GSK’s HIV drug for patients with limited options
The oral treatment from the company’s HIV unit, ViiV Healthcare, has been approved for adults whose HIV infection could…
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USFDA launches Project Patient Voice for Cancer Trials
The FDA will use this feedback to consider improvements to the website in order to make the information as user-friendly as…
FDA approves first treatment option specifically for patients with epithelioid sarcoma
Until now, there were no treatment options specifically for patients with epithelioid sarcoma. The approval of Tazverik provides a…