Top Stories
The department gave Moderna $8.2 million to accelerate development of an mRNA-based Zika vaccine.
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Concerns have emerged that continued growth in the biosimilars market could be limited by mounting pressure to push down on prescription drug outlays.
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EXPERT INTERVIEW
David Mayers, president of Wellspring Pharma Services sat down with Pharmaceutical Technology to discuss the manufacture of controlled substances.
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Natoli Engineering's Press Set-Up Tool Boxes contain everything you need to properly set up your company's tablet press easily and quickly without damaging expensive punches and dies. Each heavy-duty toolbox comes fully customized with all the necessary tools and accessories for your specific press model. Order by machine type and number of stations. Available for special or modified tablet presses.
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Supplier News
As part of a planned process to replace venture-capital financial partners, Suanfarma S.A. has acquired a stake in Idifarma.
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Capsugel is expanding the facility to meet demand for micronization services for clinical and commercial manufacturing.
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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
The companies launched Onduo, a joint venture focused on developing solutions to assist patients with Type 2 diabetes.
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Horizon Pharma will acquire Raptor Pharmaceuticals with the transaction expected to close in the fourth quarter of 2016.
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Regulatory News
Regulatory agencies meet to discuss approaches to the development of antibacterial agents.
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FDA issued a warning letter to Lima & Pergher Industria e Comercio S/A for CGMP violations.
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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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PEER-REVIEWED RESEARCH
Swab recovery parameters are reviewed in detail to define best practices and highlight common mistakes to assure successful recovery studies using a risk-based approach.
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MANUFACTURING
The media blitz surrounding drug shortages has stopped, but critical medications that have no substitutes remain in short supply. Can new approaches turn this situation around?
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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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PROCESS DEVELOPMENT
In the pharmaceutical factory of the future, data collected by internet-connected manufacturing equipment improves operational efficiency.
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FACILITIES
Renovating a facility requires careful design and a plan to minimize production interruption.
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New Trends in Hygienic Diaphragm Valves that Improve Reliability
Live Webcast: Thursday, September 22, 2016 at 11:00 EDT
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AAPS Planning Guide
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Catalent’s OptiForm® Solution Suite combines both predictive and high throughput screening technologies to identify the most stable and efficient drug form for small molecules.
AAPS Booth # 901
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Pfizer CentreOne™ is a global CMO that focuses on API synthesis and sterile injectables fill-finish.
AAPS Booth # 434
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Delivering pharmaceutical and nutraceutical performance, Ashland provides solutions for applications in tablet binding, film coating and disintegration, controlled-release formulation and drug solubilization.
AAPS Booth # 927
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Best Practices for Effective Excipient Sourcing and Testing
Live Webinar: Tuesday, September 20, 2016 at 11:00am EDT
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Events
September 18-21, 2016
September 26–28, 2016
October 4–6, 2016
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Sustained-Release Formulation: Overcoming Key Challenges Like Alcohol-Induced Dose Dumping
On Demand
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REFERENCE BOOKS |
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A three-volume set of drug delivery system handbooks. A compilation of articles related to methods and processes of manufacturing and administering pharmaceutical compounds to achieve therapeutic effects. Topics include the development of controlled-release formulations and reformulating injectable drugs for oral delivery.
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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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