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Top Stories
A change in the tax code could help the company create more jobs in the United States, while fewer FDA regulations could help reduce drug prices, according to Pfizer CEO Ian Read.
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In promising to expedite and simplify the FDA approval process, President Donald Trump fails to take account of industry's appreciation of an efficient, rigorous FDA regulatory system.
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PODCAST
Jonathan Knight, vice-president of New Product Development at Cambrex Corp., discusses the environmentally friendly, economical process route that won CPhI's 2016 award for innovation in APIs and intermediates.
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2017 PDA Annual Meeting
The 2017 Annual Meeting, the theme of which is Manufacturing Innovation: The Next Wave of Sterile and Biopharmaceutical Science, Technologies & Processing, will look ahead to the future of bio/pharmaceutical science and technology. Explore current and future trends in advanced therapeutic strategies, immunotherapy, gene-based personalized medicine and cell-based therapies, next-generation processing and facilities and big data applications for process design and optimization.
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Industry News
FDA's Warning Letter to an Indian API manufacturer alleges cGMP violations and improper cleaning and validation.
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Research by Pew Charitable Trust and ISPE suggests that inability to forecast internal demand, and poor partner alignment are among the reasons for drug shortages.
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Supplier News
Operational improvements at Pall contributed to the overall growth in the Danaher life-sciences sector.
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On a recent call, Catalent revealed that it has reached more than 90% of its current capacity and discussed how tax policy changes could affect the outsourcing industry.
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See machinery in action. Discover packaging innovations. Learn about breakthroughs and best practices. For pharma and medical device manufacturing professionals, PACK EXPO East and the Healthcare Packaging and Processing Conference have it all! Head to Philadelphia next month for solutions from 400+ exhibitors—including 200+ pharma industry suppliers—and get answers to critical issues from 30 education sessions.
 Register today at packexpoeast.com! |
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Bio/Pharma News
The investment will be used to advance Nemaura's R&D programs, which include liquid vaccines that have been reformulated for administration through the skin using its micropatch drug delivery technology.
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According to results from the FOURIER trial, Repatha significantly reduced the risk of cardiovascular events and death in patients with atherosclerotic cardiovascular disease.
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Regulatory News
The warning letter cited GMP violations for finished drug products.
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Pharmco Laboratories received an FDA warning letter for significant violations of CGMP for finished drugs and APIs at its Florida, US facility as well as misbranding of over-the-counter (OTC) acne and sunscreen drug products.
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Pharmaceutical Technology's PharmaMarketplace
Your Connection to Global Pharmaceutical Manufacturing Suppliers
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VIEWPOINTS
Translating campaign promises to predictions for bio/pharma is difficult, but optimism prevails.
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PACKAGING
Advances in materials and equipment for pharmaceutical blister packaging protect quality and enhance shelf life.
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Events
February 27–March 2, 2017
March 5–9, 2017
March 22–24, 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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