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November 10, 2022
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  GMP Carbon-14 Labeled API Manufacturing

Moravek is recognized internationally as a leading provider of GMP carbon-14 labeled APIs for use in early-phase clinical trials. Over 100 GMP APIs have been produced in compliance with FDA guidance, and all have successfully met client, CRO, and regulatory requirements.

Moravek offers outstanding CDMO capabilities and has substantial experience seamlessly coordinating concurrent progress of both CDMO and CRO activities.


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» Industry News
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  GHO Capital and The Vistria Group to Acquire Alcami
Global Healthcare Opportunities, or GHO Capital Partners LLP and The Vistria Group announced that ... read more »
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  Quanticate Announces Plans to Accelerate Growth in North America
Quanticate, a global data-focused clinical research organization (CRO), has announced plans for ... read more »
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  Insilico Medicine Signs Research Collaboration with Sanofi Worth Up to $1.2B
Insilico Medicine, a clinical stage artificial intelligence driven drug discovery company, announced... read more »
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  Charles River Announces Cell Therapy Manufacturing Capacity Expansion
Charles River Laboratories International, Inc. announced the expansion of its cell therapy contract ... read more »

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» Featured Articles
EVENT   Upright Liquid Nitrogen Biorepositories: Safer, More Reliable and Controllable with Faster Freeze Times
In the pharmaceutical and medical industries, cryogenic freezers are utilized as biorepositories for... read more »
EVENT   A Quarterly Review of New Drug Applications April - June 2022
This quarterly review on New Drug Applications (NDAs) contains data on applications approved for the... read more »
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» Featured Partners
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  UpTempo Virtuoso™ AAV Platform

Catalent’s UpTempo Virtuoso™ adeno-associated virus (AAV) platform process accelerates gene therapy development, delivering clinical material in 9 months. With a simplified supply chain, manufacturing efficiency, and standardized documentation, the scalable platform can significantly reduce the time from gene to clinic. read more »
» Featured Video
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  Documentary: Cell & Gene Therapy: Advancing the Next Generation of Pharmaceuticals
In this documentary, American Pharmaceutical Review and Pharmaceutical Outsourcing magazine spoke with industry experts to learn how cell and gene therapies are changing the healthcare landscape and ... read more »
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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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» Featured White Papers
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 »
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 »
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» More Services
Drug Formulation Learn More
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» Service Directory
Pharmaceutical Manufacturing Search More
Clinical Trial Project Management CRO Search More
Recombinant Protein Bioprocess Services Search More
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| Events
EVENT
  2023 PDA Annual Meeting
New Orleans, LA –  04/03/2023
The PDA Annual Meeting is the premier meeting on pharmaceutical/biopharmaceutical manufacturing science and technology.
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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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