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FDA Archives - Page 2 of 3 - The Pharma Times | Pharma & Health Care News Portal

FDA

Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A. Receive Breakthrough Therapy Designation from FDA

For LENVIMA (lenvatinib) plus KEYTRUDA (pembrolizumab) Combination Treatment as Potential First-Line Treatment of Patients with Advanced Unresectable Hepatocellular Carcinoma Not…

5 years ago

Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A. Announce U.S. FDA Grants Breakthrough Therapy Designation for LENVIMA

In Combination with KEYTRUDA as Therapy for Previously Treated Patients with Advanced and/or Metastatic non-MSI-H/pMMR Endometrial Carcinoma Tokyo, August 05,…

6 years ago

Eisai Signs Collaboration Agreement for Anti-Obesity Agent Lorcaserin in China to CY Biotech

Tokyo, August 04, 2018: Eisai Co., Ltd. announced today that it has entered into an agreement to grant exclusive development…

6 years ago

The FDA just approved a drug to treat smallpox in case of a bioterrorism attack – here’s why that scenario is so scary

Most of us don’t get the smallpox vaccine anymore, which means we’d be vulnerable to a bioterrorism attack using the…

6 years ago

WuXi STA Changzhou Site Passes First U.S. FDA Inspection

The integrated R&D and manufacturing facility is expecting more products to go into commercial production post approval Shanghai, May 11,…

6 years ago

Validation services for the pharmaceutical industry

New Delhi, May 05, 2018: Porvair Filtration Group, an international leader in filtration and separation, offers validation services for its…

6 years ago

MES Launches YO® Home Sperm Test in India

First FDA approved device to determine moving sperm (a key to male fertility) Test your sperm from the comfort of…

6 years ago

Personalised medicines, intelligent packaging and FDA deadlines seen as major trends for pharma packaging in 2018

Experts forecast the industry’s biggest developments at Pharmapack Europe Paris, April 21, 2018: Pharmapack Europe (#pharmapackeu) – organised by UBM – closed…

6 years ago

Lupin gets tentative USFDA approval for Testosterone gel

Mumbai, April 21, 2018: Pharma major Lupin on Wednesday said that it has received tentative approval for its Testosterone Gel, 1.62…

6 years ago

Food and Drug Administration (FDA) Assam, Magic Bus and Nestlé India commemorate World Health Day in Guwahati

New Delhi, April 08, 2018: Nestlé India in collaboration with the FDA Assam and Magic Bus India Foundation, commemorated the forthcoming…

6 years ago