Under the terms of the agreement, Sartorius Stedim Biotech will manufacture membrane adsorber technologies for GE, which will be marketed as part of GE's ReadyToProcess product offerings. / read more /
Growth is said to be driven by the deeper penetration of biosimilars in developed and emerging markets as a result of clearer regulatory pathways. / read more /
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The Pre-Connect Congress will explore pharma industry trends, such as mergers and acquisitions, the biologics market outlook, and innovation in drug delivery among others. / read more /
Label Vision Systems (LVS) will be fully integrated into Microscan and the LVS name will become a brand within Microscan's barcode label verification portfolio. / read more /
Novo Nordisk plans to invest approximately $2 billion over the next five years in new production facilities in Clayton, North Carolina, US and Måløv, Denmark. The facilities are expected to be operational during 2020. / read more /
In a new draft guidance, FDA proposes the use of a nonproprietary name plus a four-letter suffix to identify all biologic products, both new and old. / read more /
Contract development and manufacturing organizations join forces to address legislative, regulatory, and business concerns in the Pharma & Biopharma Outsourcing Association. / read more /
Currently, pharma has only scratched the surface of the potential value of repurposing drugs, says consultant Hermann Mucke. Contract service partners are playing a more prominent role, but could play an even larger one in these efforts. / read more /
CAPMUL® — Where Formulation Begins™
ABITEC's CAPMUL bioavailability enhancers are medium-chain mono- and di-glycerides and propylene glycol esters. These functional lipid excipients act as solubilizers and emulsifiers in oral, topical, transdermal, and parenteral drug delivery systems.
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The Risk and Compliance Paradigm: Risk Management's Impact on QMS
Risk Management is everywhere, and is not some lofty strategic element that is limited to top floor suits making enterprise-wide decisions. Risk Management is becoming an integral part of the compliance process. There are many ways to look at Risk, and each industry has developed different risk based tools to suit their specific business needs. / Read More /
BioTrak™ Real-Time Viable Particle Counter for immediate notification of microbial excursions
Detecting changes in levels of airborne microbiological contamination in real time in all areas of a life science manufacturing facility is now a reality. Instruments such as TSI's BioTrak™ Real-Time Viable Particle Counter facilitate proactive Quality Assurance based approaches. / Read More /
Winning Solutions for the Entire Pharmaceutical Lifecycle Pharma EXPO brings together solutions designed to give pharmaceutical, biopharmaceutical, medical device and nutraceutical companies like yours a competitive edge. Plus, the co-location with PACK EXPO Las Vegas provides the opportunity to explore processing and packaging ideas from all other industries. / Register now at pharmaexpo.com /
As challenging new formulations are developed, how prepared is your team to optimize the formulation performance in encapsulation? This webinar will provide insight into improving productivity in the use of capsules for pharmaceutical products for both the formulator and supply chain. Capsule filling technologies, dosing options, excipients, capsule selection, and other factors will be discussed. An example from the field will illustrate encapsulation practices. Sponsored by Capsugel
On Demand Learn about adaptive clinical trials, patient recruitment strategies, and advanced biomarker analysis tools designed that can accelerate drug development and clinical testing processes. Sponsored by SGS
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, be more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects. / Click here /
