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February 16, 2023
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Newsletter Sponsor
  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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  Catalent Completes Expansion of Singapore Clinical Supply Facility for Increased Temperature-Controlled Capabilities
Catalent has completed an expansion project for its clinical supply facility in Singapore at a cost ... read more »
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  Astrea Bioseparations to Combine with Biotage AB
Global life sciences platform, Gamma Biosciences, which was created by KKR to serve the advanced ... read more »
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  Biodextris Invests in a New Biologics Contract Development and Manufacturing Centre (CDMO)
Biodextris Inc., a subsidiary of Clean Biologics SAS, announced the development of a new industrial-... read more »
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  Quotient Sciences Expands Formulation Development Capabilities to Further Accelerate Drug Development Timelines
Quotient Sciences announced that it has completed an expansion of its early-phase formulation ... read more »

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» Featured Articles
EVENT   Adapting Skills to the New Data-Centric Regulatory Environment
As a data-centric approach becomes the new regulatory reality, product information managers and ... read more »
EVENT   Realizing the Potential of RWE with the Right CRO
Over the past few years, the number of regulatory submissions that include real-world evidence (RWE)... read more »
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» Featured Partners
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  Catalent’s Case Management Service

Designed specifically to address the unique challenges associated with the safe and timely delivery of advanced therapies to patients, Catalent’s Case Management Service provides professional supply chain oversight from a program’s start to finish, for each dose and every patient. 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: Shaping the Future of Formulation Development with Melt-based 3D Printing Technologies
In this whitepaper, the use of 3D printing to overcome challenges during formulation development is explored, with a focus on enhancement of ... read more »
EVENT   Whitepaper Download: The Viscosity Reduction Platform: Viscosity-Reducing Excipients for Improvement of Filtration Processes
Protein viscosity is a major challenge in preparing highly concentrated protein formulations suitable for subcutaneous injection. Highly viscous ... read more »
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» More Services
Contract API Manufacturing Learn More
Contract Analytical Services Learn More
GCP Clinical Auditing Services Learn More
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» Service Directory
Pharmaceutical Clinical Study Design Services (CRO) Search More
Preclinical Pharmacology Services Search More
Pharmaceutical Testing Equipment Search More
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| Events
EVENT
  BIO International Convention
Boston, MA –  06/05/2023
BIO is the world’s largest advocacy association representing member companies, state biotechnology groups, academic and research institutions, and ...
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EVENT
  INTERPHEX 2023
New York, NY –  04/25/2023
INTERPHEX is the leading global event that fuses industry innovation with expert-led technical conference. It’s where the newest ideas are shared, ...
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