Top Stories
Operations at Catalent's Beinheim, France, softgel facility were suspended following suspected deliberate action to misplace capsules.
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AstraZeneca's solid-dose facility in Taizhou, China received ISPE's FOYA 2015 Overall Winner award.
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Industry News
An ABPI report found a lack of quality candidates for high-skilled roles in areas such as bioinformatics, translational medicine, clinical pharmacology, and pathology.
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Lawsuit alleges birth control packaging error led to 113 unwanted pregnancies.
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Supplier News
GE Healthcare Life Sciences and Emerson Process Management collaborate in biopharmaceutical manufacturing processes.
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Consort Medical has combined and integrated Aesica's drug formulation, manufacturing, and packaging capabilities with Bespak’s drug-delivery device design, development, and manufacturing services.
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Bio/Pharma News
The University of Pittsburgh partners with biopharmaceutical company, Shire plc, to research rare diseases.
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Roche will invest in Switzerland but leave sites in Ireland, Spain, Italy, and the US as it focuses on lower-volume, specialized medicines.
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Equipment Showcase
The NP-400 is an economical, heavy-duty, medium output rotary tablet press designed, engineered and manufactured in the United States. Capable of running 24/7, the NP-400 can produce up to 180,000 tablets per hour. This single footprint press continuously monitors tablet pre-compression, main compression forces and tablet ejection force. Tablet take off force, press temperature and humidity monitoring are also available.
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Regulatory News
The new executive director of the European Medicines Agency begins appointment.
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FEATURED TOPICS |
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PARENTERALS
Although shortages, quality, and regulatory challenges remain, improved technologies and new investments suggest that the worst may be over.
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SOLID DOSAGE
Industry experts share insights on the advances in tablet coating technologies and the potential of continuous coating in solid-dosage manufacturing.
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PACKAGING
Delamination of glass packaging is a source of particulates in parenteral drugs, but identifying the root cause allowed the design of an improved manufacturing process for glass vials.
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SUPPLY CHAIN
Virtual pilot programs examine scenarios that may occur while implementing serialization requirements for the US Drug Supply Chain Security Act.
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Best Practices for Effective Product Transfer
LIVE WEBCAST: Wednesday, January 20, 2016 at 11:00am EST
Understanding all aspects of the product transfer process is critical to a successful transfer and delivery of a quality product. During this one-hour webinar, regulatory and pharma experts will discuss the critical elements and processes needed for an effective, compliant product transfer process and successful end results.
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Webcasts
On Demand
Join this informative webinar, presented by the team at Eurofins Lancaster Laboratories, to learn about the various aspects of cell banking and cell line characterization, including GMP production master and working cell banks, GMP non-production (e.g. bioassay) master and working cell banks, R&D cell banks or banking for end of production cells.
Sponsored by Eurofins Lancaster Laboratories |
On Demand
Learn basics of water activity and the role it plays in the chemical stability, microbial content, and physical properties of pharmaceutical products. Hear experts discuss compendial and regulatory requirements for water-activity determination, and practical applications of water activity in marketed pharmaceuticals.
Sponsored by Decagon Devices
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REFERENCE BOOKS |
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A compilation of informative, useful articles from Pharmaceutical Technology 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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This eBook features articles on sterility testing, disposable technologies, parenterals, facility planning, mAb formulation, and more.
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