Top Stories
AstraZeneca entered a collaboration with Bicycle Therapeutics for the identification and development of bicyclic peptides.
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FDA and BARDA awarded a contract to Continuus Pharmaceuticals to develop an end-to-end continuous manufacturing process for solid-dosage drugs.
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Industry News
The commission approved future plans, appointed members, and adopted texts during its November 2016 session.
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Researchers test the efficacy of a new polymer that is an alternative to PEG for drugs used to treat type 2 diabetes.
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EXPERT INTERVIEW
David Mayers, president of Wellspring Pharma Services sat down with Pharmaceutical Technology to discuss the manufacture of controlled substances.
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Supplier News
Recipharm and Laccure AB signed a commercial collaboration for the manufacture and delivery of Laccure's bacterial vaginosis treatment.
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WMFTG acquired Aflex Hose adding polytetrafluoroethylene-lined flexible hoses to its fluid path product portfolio.
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Bio/Pharma News
Takeda will invest more than 100 million Euros to build a new manufacturing plant for its dengue vaccine candidate in Singen, Germany.
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Boehringer Ingelheim and China Southeast University announced a joint research collaboration to develop new regenerative treatments for hearing loss.
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There are 5 different guiding and regulating agencies for cGMP mapping processes. This document summarizes the agencies and the specific articles that should govern your mapping project in warehouses, production facilities, rooms and chambers.
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Regulatory News
The UK's NICE recommended pembrolizumab for the treatment of patients with advanced lung cancer, reversing the institute's earlier decision.
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The House-approved 21st Century Cures legislation supports initiatives for medical research, drug development, and faster approvals, but comes up short on actual appropriations.
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The 2017 PDA Pharmaceutical Quality Metrics and Quality Culture Conference, Feb. 21-22, presents the first opportunity to address the FDA's revised draft guidance on quality metrics. Through plenary sessions and panel discussions, industry and regulatory experts will explore what has changed in the FDA's newest guidance, the benefits to industry and patients, and potential challenges to implementation across various segments of the pharmaceutical industry.
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Pharmaceutical Technology's PharmaMarketplace
Your Connection to Global Pharmaceutical Manufacturing Suppliers.
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VIEWPOINTS
With technology advances, continuous manufacturing shows steady progress to more widespread adoption.
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QUALITY
The authors describe some cases of container closure design flaws and actions taken by FDA to mitigate safety risks and increase patient acceptability.
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Events
January 9–13, 2017
February 1–2, 2017
May 16–18, 2017
more events |
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REFERENCE BOOKS |
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A three-volume set of drug delivery system handbooks. A compilation of articles related to methods and processes of manufacturing and administering pharmaceutical compounds to achieve therapeutic effects. Topics include the development of controlled-release formulations and reformulating injectable drugs for oral delivery.
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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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