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User fee reauthorizations, a hiring freeze, and opioid epidemic await the new FDA commissioner Scott Gottlieb.
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Forecasts were lowered, Reuters reported, due to reduced drug approvals and increased competitive pressures.
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The program aims to make biosimilars for the treatment of cancer more widely available in middle- and low-income countries.
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CPhI NORTH AMERICA SESSION
The Contract Services Market: Status and Strategies
Industry expert Jim Miller, president of PharmSource Information Services, will share his perspective on the contract services landscape and suggest strategies for outsourcing companies looking to grow in this sector.
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Get these 5 mapping resources that will make your next mapping project easier and more efficient. Learn about the proper number of sensors, calibration recommendations, warehouse mapping, regulations and guidelines, and choosing the best sensor.
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Industry News
EMA and the European Commission released a biosimilars information guide for health professionals during the EC's biosimilars conference.
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More stringent R&D investment requirements for PhRMA membership reduces the association ranks by 22 associate and member companies.
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Supplier News
The company is the first multi-site excipient supplier to achieve accreditation across production facilities.
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Operated by BioOutsource, Sartorius' subsidiary, the Glasgow, UK-based service center will offer physicochemical properties and structural attributes testing and allow clients to perform structural and functional analyses in parallel.
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Pharmaceutical Technology's PharmaMarketplace
Your Connection to Global Pharmaceutical Manufacturing Suppliers
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Bio/Pharma News
Novartis entered separate license agreements with bluebird bio and Celyad for patents related to the manufacture of CAR-T cells.
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Licensing agreement will expand Oxford Genetics bio-therapeutic discovery, design, and development service business.
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Regulatory News
FDA hopes to better use global resources and avoid duplicate inspections of foreign facilities.
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The agency sent a warning letter to Sal Pharma for not disclosing information about API manufacturers to customers.
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MANUFACTURING
Value-based medicine is putting patients at the center of pharmaceutical R&D and forcing the industry to move from treatment to prevention.
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FILL/FINISH
The author discusses the impact of prefilled syringe product contact materials and the filling and stoppering process on protein aggregates.
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Events
May 16–18, 2017
May 21–24, 2017
June 7–8, 2017
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REFERENCE BOOKS |
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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.
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eBOOKS
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Quality issues can appear at any stage of the bio/pharmaceutical development and manufacturing supply chain. Drug companies must monitor raw materials, suppliers, contract service providers, facilities, manufacturing processes, and production workers. In this e-book, the editors examine current quality issues, and how the industry is addressing quality challenges throughout the supply chain. |
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