A recent survey suggests that 36% of pharmaceutical companies and contract development and manufacturing companies have not started working on serialization, and that those who are working on it are focusing on basic compliance rather than potential long-term business benefits. / read more /
Catalent has signed an agreement with Therachon to support preclinical and clinical development of TA-46, a novel protein being developed to treat achondroplasia. / read more /
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Aptar Pharma's e-Lockout device uses advanced electronic technology to limit the number of doses available during a 24-hour period, thereby ensuring safe patient compliance to Takeda's pain-relieving nasal spray. / read more /
The companies entered a license agreement that includes Sangamo's SB-525, one of the company's lead product candidates for the treatment of Hemophilia A. / read more /
The Identification of Medicinal Products (IDMP) standards requires regulatory teams to efficiently collate data from multiple sources and functions. / read more /
Nexera UC/s
Shimadzu's new Nexera UC/s (SFC/UHPLC switching system) allows measurements by liquid chromatography (LC) and supercritical fluid chromatography (SFC) on a single system. / Read more/
Quantum
Judges at this year's International Pharmaceutical Expo 2017 (INTERPHEX) have hailed Watson-Marlow Fluid Technology Group's Quantum peristaltic pump as 'cutting-edge'. / Read more/
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 /
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.
