Top Stories
A KPMG survey reveals that approximately 84% of pharma and medical device executives plan to add jobs in next 12 months.
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Researchers at the ARC Centre of Excellence in Convergent Bio-Nano Science (CBNS) in Melbourne, Australia have developed a drug-delivery technology that circumvents first pass metabolism in the liver, thereby, enabling higher drug levels to reach the systemic circulation.
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EXPERT INTERVIEW
Jennifer Zieverink, senior director of marketing and alliance management at Aprecia, and Grant Brock, vice-president of engineering at Aprecia, spoke with Pharmaceutical Technology about the company's ZipDose Technology, which is a three-dimensional printing technology used to make solid-dosage drugs.
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Industry News
A new study reveals a potential new approach to treat sickle cell disease and beta thalassemia using CRISPR-Cas9 gene-editing technology.
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CPhI Pharma Awards' panel doubles in size and welcomes experts from around the world.
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Supplier News
Agilent Technologies announces plans to build a new oligo manufacturing facility in Colorado that will double current capacity.
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The GMP-certified facility will produce TruTag microtags for global pharmaceutical customers.
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Need a cost-effective but world-class tablet press? Make the NP-155 your #1 choice! This economical beauty was built to last with direct drive gears for greater reliability. With a hardened steel die table, 3-point gravity feed frame, and touch-screen HMI control, this machine is a fantastic mix of precision and beauty. Capable of more than 280,000 tablets per hour,  Read more on the NP-155 now!
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Bio/Pharma News
The EDA offered Allergan tax credits in order to encourage the company to remain in the state.
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Sustained-Release Formulation: Overcoming Key Challenges Like Alcohol-Induced Dose Dumping
LIVE WEBCAST: Tuesday, September 13, 2016 | 11 am EDT | 10 am CDT | 8 am PDT
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Regulatory News
Zika vaccine development is hindered by technical challenges and funding shortfalls.
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Understanding the Relationship between Critical Quality Attributes and the Microstructure of Topical Semi-Solid Formulations
LIVE WEBCAST: Thursday, September 8, 2016 at 11 am EDT | 10 am CDT | 8 am PDT
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MANUFACTURING
A technology management process identifies and evaluates new technologies in biopharmaceutical manufacturing to aid business decisions.
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FORMULATION
Industry experts discuss key considerations in the development of orally disintegrating tablets.
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Amorphous Dispersion Drug Formulations: A Modern Simulation-Based Approach
LIVE WEBCAST: Wednesday, September 7, 2016 at 11 am EDT
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DRUG DELIVERY
A Q&A with FDA to gain insight on FDA's views of three-dimensional printing and its regulation in drug manufacturing.
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Webcasts
On Demand
An understanding of the variable process parameters that have a significant impact on the final pharmaceutical product is necessary to successfully manage a hot-melt extrusion process when using twin-screw extrusion. Experts will discuss residence time, mechanical-energy consumption, and other critical parameters, as well as their effects on a scientific approach to process scale-up.
Sponsored by Thermo Fisher Scientific |
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On Demand
Capsugel Dosage Form Solutions will present a webinar discussing the aspect of engineering spray-dried dispersion properties, with a particular emphasis on the impact of atomization and drying rate on powder mechanical properties.
Sponsored by Capsugel
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Events
September 12-14, 2016
September 18-21, 2016
September 26–28, 2016
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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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