Synopsis : – Sun Pharmaceutical Industries Limited announced that one of its wholly owned subsidiaries has received Emergency Use Authorization (EUA) from…
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Tag:
Approval
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CompaniesMerck & Co
European Commission Approves Merck’s Pneumococcal vaccine Vaxneuvance (Pneumococcal 15-Valent Conjugate Vaccine) for Individuals 18 Years of Age and Older
by adminby adminSynopsis : – The administration of the vaccine in accordance with the official recommendation can effectively prevent invasive disease and pneumonia caused…
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Summary – Gland Pharma Limited has recently received a tentative approval from the United States Food and Drug Administration (USFDA) for Cangrelor…
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CompaniesPfizerPharma Science & Research
Swissmedic Approves Pfizer/ BioNTech Vaccine for Children Over 5
by adminby adminSummary: The clinical trial results show that the vaccine is safe and effective in this in this age group, it will thus…
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AstraZenecaCovid DrugsRegulatoryU.S FDA
FDA Approves AstraZeneca’s Evusheld becomes First Authorized COVID Antibody to Protect the Immunocompromised Before Exposure
by adminby adminSummary : With the FDA’s emergency use authorization today of AstraZeneca’s long-acting antibody cocktail, the roughly 2% of U.S. residents who are…
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434 RC meetingCIBRC - Indian Pesticide ApprovalsRC Meeting updates
INDIAN PESTICIDE APPROVAL UPDATES: 434th RC MEETING [CIBRC]
by adminby adminMINUTES OF THE 434th REGISTRATION COMMITTEE MEETING HELD ON 30.11.2021. The 434th meeting of the Registration Committee (RC) was held under the…
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Agrochemicals
Janssen Pharma’s Byannli (PP6M) receives European approval for Maintenance Treatment of Schizophrenia in Adults.
by adminby adminKEYPOINTS: Janssen has won approval from the European Commission for Byannli, a six-month formulation of Paliperidone Palmitate, two months after receiving a…
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Agrochemicals
The US drug major Eli Lilly files patent litigation against 20 Indian companies on Baricitinib.
by adminby adminHighlights: The US drug major Eli Lilly has filed a patent infringement litigation at the Delhi High Court against several Indian pharmaceutical…
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Nelarabine
Zydus Cadila receives USFDA Final Approval for Nelarabine Injection a Therapeutically Generic Version of Arranon injection.
by adminby adminKEYPOINTS: Zydus Cadila has received final approval from the US FDA to market Nelarabine injection 250MG/50ML in the United States. Zydus Pharmaceuticals…
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Agrochemicals
FDA Grants AppliedVR Approval for First Virtual Reality Therapeutic to Treat Chronic Low Back Pain.
by adminby adminSUMMARY: The U.S. Food and Drug Administration today authorized marketing of EaseVRx, a prescription-use immersive virtual reality (VR) system that uses cognitive…