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November 01, 2022
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  Enhance dissolution rate and lubrication with a single high performance excipient

Parteck® PLX 188 is a dissolution rate enhancing excipient that also acts as a robust water-soluble lubricant. It is a multi-functional excipient designed with the needs of modern manufacturing in mind – such as direct compression and continuous manufacturing – and ideally caters to the needs of solid dosage formulation.

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» Industry News
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  Lonza and Singzyme Announce Collaboration Agreement to Accelerate the Development of Bioconjugates
Lonza announced that it is enhancing its bioconjugation offering through an agreement with Singzyme,... read more »
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  Thermo Fisher Scientific to Acquire The Binding Site Group
Thermo Fisher Scientific Inc. announced that it has entered into a definitive agreement to acquire ... read more »
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  EpiVax Joins Intravacc, CEPI on Project to Develop Universal Betacoronavirus Vaccine
EpiVax, Inc. announces participation in a new project with Intravacc, funded by CEPI (Coalition for ... read more »
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  Terumo Pharmaceutical Solutions Expands CDMO Services Outside Japan for Global Market
Terumo Pharmaceutical Solutions (TPS), a division of Terumo Corporation (TSE: 4543) and a leading ... read more »

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» Featured Articles
EVENT   Why Registries and Natural History Studies Are Indispensable in Rare Disease Drug Development
Increasing emphasis on rare diseases has led to a greater need to accurately define the profile, ... read more »
EVENT   Diversity In Clinical Trials Drives Better Patient Outcomes - CROs Play Important Role in Operationalizing Sponsor Plans
Ensuring diversity in clinical trials is not only supported by regulatory guidance, but is critical ... read more »
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» Featured Partners
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  Integrated CDMO Services From Beginning To End

Adare Pharma Solutions is a global technology-driven CDMO providing a full spectrum of end-to-end integrated services, from product development through commercial manufacturing and packaging. read more »
» Featured Video
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  On-Demand Webinar: Navigating Impurities in Pharmaceutical Drugs
In this webinar you’ll learn: Some technical ideas and approaches to identify and determine with a high level of confidence all potential impurities and degradants. read more »
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  On-Demand Webinar: The Configurability Imperative: Untapped Potential in MES
Today’s manufacturers need a modern MES and a paperless batch record that can adapt to keep pace with evolving operational requirements. Traditional manufacturing execution systems (MES) are typically... read more »

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» Featured White Papers
EVENT   Whitepaper: Safe and Efficient Handling of High Potent Drug Products.
High potent drug products for e.g. oncology or hormone therapy will play an important role in innovative drug therapy in the future. The development ... read more »
EVENT   Whitepaper: The Developability Classification System (DCS): Enabling an Optimized Approach for Formulation of Poorly Soluble Molecules
This whitepaper explores the developability classification system (DCS), a recent advancement based on the BCS system but, instead of focusing on ... read more »
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» More Services
Commercial Manufacturing Learn More
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Pharmaceutical Vial Filling Services Learn More
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» Service Directory
Cell Panel Development for in vitro Screening Search More
Bioprocess Technology and Services Search More
Pharmaceutical Particle Size Analysis Services Search More
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| Events
EVENT
  IFPAC 2023
North Bethesda, Maryland –  06/04/2023
Process Analytical Technology is one of the most exciting and important advanced technology areas meeting both the current challenges, as well as the ...
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