Latest News in the pharma Industry

Policy & Regulation

FDA Approves Biogen Idec's Eloctate, First Hemophilia A Therapy to Extend the Interval between Prophylactic Infusions, for Both Adults and Children

FDA Approves Biogen Idec's Eloctate, First Hemophilia A Therapy to Extend the Interval between Prophylactic Infusions, for Both Adults and Children

10 Jun 2014

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SMC Makes Negative Recommendation for Abraxane, Treatment for Metastatic Pancreatic Cancer

SMC Makes Negative Recommendation for Abraxane, Treatment for Metastatic Pancreatic Cancer

10 Jun 2014

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European Medicines Agency Accepts Accelerate?d Marketing Authorisat?ion Applicatio?n for Nintedanib? in IPF

European Medicines Agency Accepts Accelerate?d Marketing Authorisat?ion Applicatio?n for Nintedanib? in IPF

5 Jun 2014

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AstraZeneca’s Novel Antibiotic Candidate AZD0914 Given Fast Track Status by US FDA

AstraZeneca’s Novel Antibiotic Candidate AZD0914 Given Fast Track Status by US FDA

3 Jun 2014

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FDA Issues Response Letter for Epigenomic?s' Colorectal Cancer Screening Blood Test Epi proColon Requesting Further Data Pre-Approv?al

FDA Issues Response Letter for Epigenomic?s' Colorectal Cancer Screening Blood Test Epi proColon Requesting Further Data Pre-Approv?al

3 Jun 2014

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Sanofi and Lilly announce licensing agreement for Cialis (Tadalafil) OTC

Sanofi and Lilly announce licensing agreement for Cialis (Tadalafil) OTC

30 May 2014

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FDA Approves First-Line Use of Vectibix (Panitumum?ab) Plus Folfox for Patients with Wild-Type KRAS Metastatic Colorectal Cancer

FDA Approves First-Line Use of Vectibix (Panitumum?ab) Plus Folfox for Patients with Wild-Type KRAS Metastatic Colorectal Cancer

26 May 2014

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FDA Approves Dalvance to Treat Skin Infections

FDA Approves Dalvance to Treat Skin Infections

26 May 2014

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European Commission Approves Third Product from the Boehringer Ingelheim and Lilly Diabetes Alliance

European Commission Approves Third Product from the Boehringer Ingelheim and Lilly Diabetes Alliance

23 May 2014

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Pharmaceutical Industry ‘Not Ready’ to Manage XEVMPD Requirements According to New ProductLife Group Research

Pharmaceutical Industry ‘Not Ready’ to Manage XEVMPD Requirements According to New ProductLife Group Research

22 May 2014

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FDA Warning Letter Says Sun Pharma Plant Hid Batch Failures

FDA Warning Letter Says Sun Pharma Plant Hid Batch Failures

21 May 2014

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FDA Guidance for Industry: ANDAs: Stability Testing of Drug Substances and Products and FDA Q&A

FDA Guidance for Industry: ANDAs: Stability Testing of Drug Substances and Products and FDA Q&A

20 May 2014

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