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Top Stories
Walmsley will succeed Andrew Witty as CEO of the British drug maker.
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The agency granted accelerated approval to Sarepta's controversial DMD treatment, under the condition the company conduct additional studies to demonstrate efficacy.
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Industry News
EMA has recommended halting supply of non-critical drugs from Pharmaceutics International Inc. because of GMP failures.
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In response to the EpiPen pricing scandal, Janet Woodcock, director of FDA's Center for Drug Evaluation and Research, clarifies FDA's role in drug pricing.
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EXPERT INTERVIEW
Richard Denk, head sales containment at SKAN, spoke with Pharmaceutical Technology about trends in handling high potency APIs.
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One week left for Natoli Engineering's September Sale. All Manesty and Stokes replacement parts are 10% off! No exceptions and no gimmicks. Order by September 30th and receive an additional 10% off our already competitive pricing. In-stock items shipped day of order. Don't delay,
 order from Natoli today! |
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Supplier News
GE Healthcare's GE BioPark Cork will hold four KUBio manufacturing facilities; GE will also collaborate with NIBRT for biopharmaceutical training.
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The project aims to address challenges facing the development, manufacture, and delivery of vaccines.
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Struggling to Maintain Quality Oversight?
Gain greater end-to-end control with harmonized operations. Read the five steps to align quality globally for faster, fact-based decision making and compliance readiness.
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Bio/Pharma News
Adaptimmune entered into a manufacturing agreement with PCT for the manufacture of its SPEAR T-cell therapies.
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Allergan will acquire Vitae pharmaceuticals for $639 million.
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Reversed Phase Liquid Chromatography using Surrogate/Additional Stationary Phases
Live Webinar: Wednesday, October 26 at 11am EDT
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Regulatory News
The agency has recommended marketing authorization for Ibrance in the European Union.
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Industry concerns have generated efforts by FDA to streamline the system for designating the lead center to regulate a new combination product.
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Strategies for IND Filing Success
Live Webinar: Friday, October 21 at 11:00am EDT
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Employing a Lean Lab Approach to Optimize Lab Processes: Part 2 “Improve Productivity”
Live Webinar: Tuesday October 11 at 11am EDT
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QUALITY
Visual inspection of parenteral vials is the first step in a root cause investigation.
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FORMULATION
Nanoparticulate technologies are showing promising potential in delivering both small-molecule drugs and biomacromolecules across the blood brain barrier.
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Don't Let Your Diluent be the Weakest Link in Your Drug Product
Live Webinar: Thursday, October 13 at 10:00am EDT
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AAPS Planning Guide
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The FE75 double-sided rotary tablet press is equipped with up to 115 punch stations to produce more than 1.6 million tablets/hr.
AAPS Booth # 1133
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Qualicaps is a global manufacturer of empty pharmaceutical capsules and pharmaceutical processing equipment.
AAPS Booth # 827
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Lubrizol LifeSciences is a healthcare solution partner for medical and pharmaceutical manufacturers who need product development support and combination device solutions.
AAPS Booth # 1127
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Getting the Full Picture Predicting Protein Stability Using Chemical and Thermal Denaturation
Live Webinar: Thursday, September 28 at 11:00am EDT
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Events
September 26–28, 2016
October 4–6, 2016
November 7–8, 2016
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Enabling Formulation of Water-Soluble and Water-Insoluble Molecules Using a Lipophilic Salt Approach
Live Webcast: Tuesday, September 27 at 11:00 EDT
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REFERENCE BOOKS |
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Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development.
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eBOOKS
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Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems. |
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