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PRODUCTION TRENDS
Civica Rx plans redundant manufacturing capacity to relieve and prevent shortages of generic, sterile injectable drugs.
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IFPAC REPORT
Tools help improve understanding of excipient risk in formulating OSD drugs.
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COVID-19 NEWS
Suppliers to the bio/pharma industry are sharing news about the business operations during the global COVID-19 pandemic. To view current information about the company’s business operations, click the company name.
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The agency has been tasked with coordinating efforts to mitigate shortages of medicines within Europe during the COVID-19 pandemic.
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PACKAGING
Functional packaging protects temperature-sensitive drugs.
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More Packaging
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EDITOR'S PICKS
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The GEA Hilge Novatwin hygienic twin-screw pump line can be used for products or as a clean-in-place (CIP) pump.
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Enhancements to Augury’s AI-based machine health platform include new capabilities and collaboration tools.
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WEBCASTS
Integrated Preformulation Studies for Fast Advancement of Drug Candidates to Human Clinical Studies
Wednesday, April 15, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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Leveraging Digital Assistance to Address Oral Solid Dosage Formulation Challenges
Tuesday, April 21, 2020 at 9am EDT| 2pm BST| 3pm CEST
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When Drug Meets Device: How to Assess Compatibility
Tuesday, May 19, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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Through Container Verification of Pharmaceutical Raw Materials with the New Agilent Vaya Handheld Raman System
Europe Broadcast: Thursday, May 14, 2020 at 9am EDT | 2pm BST | 3pm CEST
US Broadcast: Thursday, May 14, 2020 at 2pm EDT | 1pm CDT | 11am PDT
Asia Pacific Broadcast: Friday, May 15, 2020 at 8:30am IST | 11am CST | 12pm JST | 1pm AEST
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EVENTS
July 15–July 17, 2020 | New York, NY
Now July 20–July 22, 2020 | Raleigh, NC
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eBOOK
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The Pharmacopoeia Compliance Series features a description of ways bio/pharma companies can participate in monograph development, a practical approach to pharmacopoeial compliance, and a summary of this 12-part series. Other features include a review of FDA’s efforts to maintain the quality of the drug supply during the COVID-19 pandemic, a review of FDA’s new cell and gene therapy guidance documents, and recommendations for maintaining data integrity.
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