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FDA Approves Phase 1 Clinical Trials for NewLink Genetics’ Ebola Vaccine
FDA gives NewLink Genetics approval to proceed to Phase 1 clinical studies of Ebola vaccine.
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The Risk and Compliance Paradigm: Risk Management's Impact on QMS
Risk Management is everywhere, and is not some lofty strategic element that is limited to top floor suits making enterprise-wide decisions. Risk Management is becoming an integral part of the compliance process. There are many ways to look at Risk, and each industry has developed different risk based tools to suit their specific business needs.
Get a glimpse at how compliance industries are utilizing risk as a core benchmarking metric for decision-making in the enterprise.
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Merck Receives Accelerated Approval of the First FDA-Approved Anti-PD-1 Therapy
KEYTRUDA was approved for the treatment of unresectable or metastatic melanoma and disease progression.
PDA Announces Technical Report on Drug Shortages
PDA will publish a technical report on quality risk management aspects of drug shortages in early 2015.
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As the innovative leader in tablet compression tooling, presses, accessories, and services, Natoli Engineering Company strives to provide customers with new ways to keep in touch, stay educated, and ease the order process. Our completely redesigned website features simpler navigation, online quoting with photos of press parts and accessories, and more! Search Natoli's parts catalog by OEM part number, manufacturer, and machine.  Check it out. |
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Natoli Engineering Opens Natoli Institute for Industrial Pharmacy Research and Development
Natoli Engineering Company partnered with the Brooklyn campus of Long Island University to open the Natoli Institute for Industrial Pharmacy Research and Development.
DPT Laboratories Acquires Media Pharmaceuticals' Lakewood Facilities
DPT Laboratories acquired Media Pharmaceuticals' Lakewood, New Jersey facilities, providing space for aseptic processing suites and filling equipment.
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Sartorius has developed a brand-new, scalable range of single-use bags based on an innovative, flexible and robust 400 µm polyethylene film. The Flexsafe product family is used to implement and establish single-use bioprocessing throughout all steps of drug manufacturing—from process development to production. The innovative concept of Flexsafe addresses key industry requirements for reliable and consistent single-use manufacturing of commercial vaccines and drugs. Learn more |
AbbVie Announces Collaboration with Calico to Develop New R&D Facility
AbbVie and Calico announce a novel collaboration to accelerate the discovery, development, and commercialization of new therapies.
University of Toronto Announces Collaboration with Janssen and Johnson & Johnson Innovation
Three-year agreement will support research on treatments for major brain disorders in Neuroscience Catalyst project.
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API Characterization for a Speedy and Successful Formulation Strategy
September 18, 2014 at 11:00 AM EDT
To Register Free: www.pharmtech.com/strategy |
Infinity and AbbVie Collaborate to Develop Oncology Drug
The companies plan to develop and commercialize duvelisib (IPI-145).
European Commission Approves RoACTEMRA for Treatment of RA
Roche’s RoACTEMRA receives EU approval for use in patients with early rheumatoid arthritis.
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Worry-free weighing: Dealing with static and drafts
Thursday, October 9, 2014 at 11:00 AM EDT
To Register Free: www.pharmtech.com/worry |
ProBioGen Plans Expansion
ProBioGen, a biopharmaceutical drug manufacturer, spends €20 million to double its workforce.
Catalent Adds Prefilled Syringe Line for Clinical Trial Supplies
Catalent’s addition of an automated prefilled syringe clinical packaging line at its Philadelphia facility will support its work with Eli Lilly.
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PharmTech Europe
25th Anniversary
Pharmaceutical Technology Europe celebrates 25 years of publishing with a retrospective of drug development trends and expert insight into emerging trends.
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Pharmaceutical Technology presents its Process Analytical Technology resource guide combo
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects.
... Click here |
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