Top Stories
Teva and IBM expanded their partnership to focus on drug development and chronic disease management.
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Douglas C. Throckmorton, MD, provides some key facts about abuse-deterrent opioids.
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EXPERT INTERVIEW
Angelo Stracquatanio, co-founder of Apprentice Field Suite, spoke with Pharmaceutical Technology about smart glasses and their use in pharmaceutical manufacturing.
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Industry News
The Czech Republic drug manufacturer was cited for data integrity and quality issues.
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Pharmapack Europe is inviting pharmaceutical packaging and drug-delivery experts to apply for the 2017 Pharmapack Awards.
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Looking for a cost effective way to increase production and reduce overhead? Multi-tip tooling from Natoli Engineering is a great way to do just that! Natoli has been producing high-quality multi-tip tooling for decades so you can rest assured we can handle even the most difficult problems. Whether you need micro-tabs or specialty shapes, trust Natoli for your multi-tip tooling needs.
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Supplier News
Ashland opened a new pharmaceutical excipient manufacturing facility in Nanjing, China.
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GENCO, a FedEx Company, introduces a multi-tenant warehouse model in Milton, Ontario, and Memphis, Tennessee.
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From Concept To Commercialization. Now Metrics Contract Services Delivers Across The Spectrum.
With an $80 million expansion underway, Metrics will soon be your solution for oral-dose pharmaceutical development through commercial manufacturing – all in one contiguous location. Learn more about our improved state-of-the-art potent facilities and our pursuit to be the most sought-after oral-dose CDMO. Visit MetricsContractServices.com/expansion.
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Bio/Pharma News
The collaboration follows the signing of a cooperative research agreement between Sanofi Pasteur, Fiocruz, and WRAIR.
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Kaléo announced that it will be reintroducing the AUVI-Q autoinjector to the US market during the first half of 2017.
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Regulatory News
TraceLink launched the EU-hosted early access program to reduce the time, cost, and risk of achieving regulatory compliance for global requirements.
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IDT Biologika will provide fill/finish services of live-vectored virus products in clinical development through licensure.
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ASEPTIC/STERILE PROCESSING
Susan Schniepp, distinguished fellow at Regulatory Compliance Associates, discusses the assessment of risk in the processing of intravenous injectable drugs.
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STANDARDS & REGULATION
Regulators are tightening up on post-marketing monitoring of biological medicines to detect deficiencies caused by manufacturing problems, particularly those stemming from post-authorization changes in the manufacturing process.
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BEST PRACTICES
Consider the purity of exhaust air emitted by vacuum pumps in addition to the purity of compressed air used in the pharmaceutical process.
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AAPS Exhibitor Guide
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ACG Worldwide is an integrated manufacturing, packaging, and R&D solutions provider for the global pharmaceutical industry.
AAPS Booth # 801
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Delivering pharmaceutical and nutraceutical performance, Ashland provides solutions for applications in tablet binding, film coating and disintegration, controlled-release formulation and drug solubilization.
AAPS Booth # 927
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CordenPharma is your full-service Contract Development & Manufacturing (CDMO) partner for APIs, Drug Products, and Packaging Services.
AAPS Booth # 1108
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Emergent BioSolutions provides contract manufacturing services for the aseptic fill/finish of vials and syringes: liquid and lyophilized products.
AAPS Booth # 611
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As a member of Eurofins' BioPharma Product Testing Group--the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide--Eurofins Lancaster Laboratories supports all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control throughout all stages of the drug development process.
AAPS Booth # 1221
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Events
November 7–8, 2016
November 13–17, 2016
November 16, 2016
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REFERENCE BOOKS |
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A compilation of articles in a three-handbook set covering general Analytical Testing and Stability in the manufacture, packaging, storing, and testing of formulated products.
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eBOOKS
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Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems. |
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