National Medical Commission (NMC) requested information from the IT department regarding the doctors whose names had recently come to light as a result of I-T raids on the Bangalore based pharmaceutical company Micro Labs.
Cyclosporine Softgel Capsules have been given the US Food & Drug Administration’s permission, according to a Bengaluru-based
company’s step-down wholly-owned subsidiary, Strides Pharma Global
Regarding its application of a so-called “patent thicket” to the most popular medication in the world, Humira, AbbVie has come under fire—as well as accusations of antitrust violations. However, the company’s legal defence has once more been successful.
Make in India and PLI programs have opened up new employment prospects in the pharmaceutical and medical device industries, providing both entry-level and experienced job candidates with opportunities for advancement.
US Food and Drug Administration has begun an inspection at the formulations facility of Sun Pharmaceutical Industries Ltd. in Mohali, Punjab. Two US FDA inspectors have begun the audit, which is expected to end this week.
The Health Ministry issued a one-page advice on dos and don’ts for monkeypox. It stated that close contact with infected individuals is the most major risk factor for monkeypox virus infection during human monkeypox outbreaks.
JUVÉDERM Volux XC from AbbVie has been given FDA approval to restore jawline definition in persons over 21 who have moderate to severe loss of jawline definition.