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PRODUCTION TRENDS
Technologies and methods for new and refurbished manufacturing facility construction expand capacity for new modalities and to ease shortages.
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INDUSTRY NEWS
Originally scheduled to take place April 28–30 at the Javits Center in New York City, the event has been rescheduled to July 15–17.
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Rapid deployment kits can facilitate tech transfer and allow for communication between operators onsite and experts offsite.
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FDA issued its first announcement of a drug shortage related to the COVID-19 coronavirus outbreak.
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Subscribers can enjoy each full issue of Pharm Tech in print, or via Pharm Tech apps.
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PACKAGING
Labeling equipment for primary and secondary packaging and a new label printer improve speed and quality.
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More Packaging
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EDITOR'S PICKS
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The new BIOSTAT STR Generation 3 with BIOBRAIN bioproduction platform offers process intensification with automated feed and bleed and integrated cell retention functionality.
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The LC light series of tablet coaters from Lödige Process Technology is designed for cost-efficient coating.
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WEBCASTS
Lonza Capsugel® – The Right Partner for Your Next Drug Development Project
On Demand
Introducing the New Portable XRF Analyzer for Identity Testing of Pharmaceutical Ionic Salts
On Demand
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Sterile Filling Challenges for Early-Phase Product Development
Thursday, March 19, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET
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How to Perform Ignition and Drying Methods Such as USP <281> and USP <731> Safely Without Sacrificing Performance
Thursday, March 26, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET
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Optimizing Equipment Availability for Capsule Fillers
Tuesday, March 24, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET
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Oral Peptide Delivery Utilizing Specialized Encapsulation Technologies
Wednesday, April 1, 2020 at 11am EDT | 8am PDT | 4pm GMT | 5pm CEST
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Integrated Pre-Formulation 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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Striving for Zero Defects: Use of Quality-by-Design Principles for Manufacturing Parenteral Packaging Components to Mitigate Risks of Drug Product Contamination
Part I: Tuesday, April 7, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CET
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Know-How to Optimize Your Project
Experience. Commitment. Integrity. Three words describing what you can expect with Pii as your CDMO – whether you’re looking to develop a sterile, oral solid dose or topical drug product. With 25 years of scientific, analytical and regulatory know-how and newly-expanded capacity for automated aseptic fill-finish, Pii is ready and eager to partner with you on your next project.
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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 editors explore novel technologies for the formulation, manufacture, purification, and delivery of sterile small- and large-molecule drugs including single-use systems, facilities and equipment, contamination issues, and process analytics.
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