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Top Stories
A mutual recognition agreement to accept inspection data from eight EU regulatory authorities may reduce inspection burdens at global drug facilities.
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The new BioLive event, which will be a global hub for biopharmaceutical manufacturing, will launch alongside CPhI Worldwide 2018 in Madrid.
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PharmTech 2017 Employment Trends
The editors of Pharmaceutical Technology invite you to participate in the annual employment survey for individuals involved in bio/pharmaceutical development, formulation, or manufacturing.
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Industry News
The M&A advisory firm has developed an interactive map of manufacturing sites to give insight into the market size of global manufacturing.
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Innovator companies are exploring new avenues to keep generic drugs at bay, says CPhI expert, but competition authorities and drug regulators will play a key role in preventing such abusive anti-competitive practices.
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Supplier News
The biotechnology company has entered a contract with the United States Army to develop custom recombinant spider silk for protective textile applications.
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Roquette has opened new facilities and an innovation center in Singapore, China that will focus on developing plant-based products.
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Bio/Pharma News
AbbVie will pay a $205-million upfront payment and have the option to develop and commercialize two antibody targets globally.
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As part of the $900-million deal, Incyte will pay $150 million upfront to develop and commercialize an anti-PD-1 drug candidate from biopharmaceutical company, MacroGenics.
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Regulatory News
Scott Gottlieb, MD, went before the House Committee on Energy and Commerce to give members the agency's view on how to fight the opioid crisis, stressing the use of long-term treatment with drug therapy.
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The vaccine is approved for the prevention of shingles in patients aged 50 years and older.
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Standards & Regulations
Just as FDA strengthens ties between reviewers and plant inspectors, proactive manufacturers are involving different disciplines in preparation for FDA audits.
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Excipients
This article seeks to promote dialogue among stakeholders to facilitate consensus regarding requirements for excipients.
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eBOOKS
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Biologics and Sterile Manufacturing
New technologies, including single-use systems, are leading the push for faster production and higher titers. At the same time, ensuring quality in raw materials and water systems, and controlling contamination are paramount. In this Biologics and Sterile Manufacturing eBook, the editors explore key technology, process, and operational topics. |
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