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Webcast: Accelerate Sterile and Non-Sterile Clinical Trial Manufacturing with Single-Use Technologies
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Webcast: Overcoming Formulation Challenges of Parenteral Drugs
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DCAT Week 2013
March 11–14, 2013
Washington, USA

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March 17–21, 2013
Philadelphia, USA

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News

Merck Pays $688 Million To Resolve Vytorin Lawsuits
Merck has agreed in principle to pay $688 million to settle two federal securities class-action lawsuits involving the company's anticholesterol drugs Vytorin and Zocor, thereby avoiding trial.
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Mylan, Biocon Form Pact to Develop and Commercialize Insulin Products
Mylan has entered into a definitive agreement with Biocon Limited, an Indian biotechnology company, for an exclusive collaboration on the development and commercialization of generic versions of three insulin analog products.
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Sanofi Invests EUR 44 Million in Genzyme Campus
Sanofi is investing EUR 44 million ($58.7 million) in Genzyme’s biotechnology campus in Waterford, Ireland.
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President Obama Plans for Healthcare Reform and Job Growth
President Obama’s State of the Union Address on Feb. 12, 2013 touched on some issues that may directly impact the pharmaceutical industry: healthcare reform, innovation, and job creation.
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Modernization of USP Standards
The US Pharmacopeial Convention contiues to make modernization of standards a top priority in 2013.
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Balancing Medicines Supply with Quality
According to FDA, 75% of the products in shortage are generic sterile injectables; low-margin products that must be manufactured in specialized facilities and that must meet stringent quality metrics.
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EMA Seeks to Expand Collaboration on Orphan Medicines
The European Medicines Agency’s Committee for Orphan Medicinal Products (COMP) is seeking to expand its international cooperation in 2013.
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Daiichi Sankyo Faces Gender Discrimination Lawsuit
Six current and former female pharmaceutical sales representatives have filed a $100-million gender discrimination lawsuit against Daiichi Sankyo in a US district court.
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Company Notes
  • Almac and DSM Pharmaceutical Products, the custom manufacturing and technology business of Royal DSM, reported the successful transfer of enzymes for enzyme screening, process development and scale-up manufacture, as part of an October 2012 agreement in biocatalysis. The agreement grants both parties access to their enzyme platform technologies and services for the manufacturing of APIs. The collaboration also enables Almac to offer its customers a preferred partner for large-scale production. Read More
  • AstraZeneca announced that, on Feb. 14, 2013, the United States Court of Appeals for the Federal Circuit summarily upheld a lower court ruling that had found the formulation patent protecting Seroquel XR (quetiapine fumarate) extended-release tablets in the US to be valid and infringed. Read More
  • DSM Pharmaceutical Products has signed a collaboration agreement with Chemtrix in the field of continuous flow chemistry. The collaboration is intended to provide equipment, development, and manufacturing services to the pharmaceutical industry. Read More
  • FDA has approved Novartis Zortress (everolimus) for the prophylaxis of organ rejection in adult patients receiving a liver transplant. Zortress is the first mammalian target of rapamycin inhibitor approved for use following liver transplantation. It is also the first immunosuppressant approved by the FDA in over a decade for use following liver transplantation. Read More
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