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September 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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  American Injectables Announces Validation of New Tampa Operation
American Injectables successfully commissioned and qualified its new facility in Tampa, Florida. read more »
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  Ashland Furthers Bioresorbable Polymers Manufacturing and R&D Capacity
Ashland announced a strategically significant expansion of its Viatel™ bioresorbable polymer ... read more »
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  QPS Adds Three to Executive Team to Enhance Its Global Medical, Regulatory and Biotech CRO Services
QPS continues to expand and align its full service preclinical, bioanalysis and clinical ... read more »
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  Worldwide Clinical Trials Builds 15,000sqft Lab in Austin, Texas
Worldwide Clinical Trials expanded its Early Phase large molecule capabilities and services with a ... read more »

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» Featured Articles
EVENT   The Pharmaceutical Industry's New Role in Redefining Healthcare
Traditional healthcare delivery has been on its way out for well over a decade now, as patient outcomes and measurable value have increased in importance. read more »
EVENT   Pharmaceutical Supply Chain Gradually Working Toward Data Interoperability for DSCSA
Progress toward the 2023 Drug Supply Chain Security Act (DSCSA) requirement for full product serialization is uneven, with some progress and obstacles appearing as healthcare supply chain partners ... read more »
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» Featured Partners
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  GMP ¹4 C-Labeled API Manufacturing

Moravek is a world-leading provider of GMP carbon-14 labeled APIs that are manufactured in compliance with FDA guidance and intended for use in early-phase clinical trials. 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: Current Strategies for Enhancing Bioavailability of Poorly Soluble Compounds: A Discussion on Commonly Used Technologies & Supporting Services
Targeted bioavailability enhancement strategies can help improve the success of early drug candidates by maximizing the API’s exposure in early in-... 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
Clinical Trial Manufacturing Learn More
Diabetes Modeling Learn More
Contract API Manufacturing Learn More
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» Service Directory
Pharmaceutical Manufacturing Search More
Clinical Research Data Management Search More
Cold Chain Management Solutions / Pharmaceutical Cold Chain Management Search More
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| Events
EVENT
  2nd Annual Aseptic Processing Conference
London, UK –  09/19/2022
The Aseptic processing industry has seen consistent growth in recent years, with advances in innovative therapeutics, the introduction of novel ... event details »
EVENT
  CPHI/ ICSE/ P-MEC/ bioLIVE/ Hi Korea 2022
COEX, Korea –  09/28/2022
From leading domestic and international companies to big pharma startups. A variety of companies with innovative technologies in the field of ... event details »
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