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May 18, 2023

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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.

	Industry News

Worldwide Clinical Trials Expands Site Alliance Collaboration to Support Oncology Trials
Worldwide Clinical Trials has expanded its Site Alliance Collaboration with new partners across the ... read more »

IntelGenx Receives Health Canada’s Amended DEL License to Conduct Third-Party Testing
IntelGenx Corp. announced that it has received an amended Drug Establishment License (“DEL”) from ... read more »

GenNext Technologies Partners with Emery Pharma on Full-Solution Biopharmaceutical Protein Footprinting Services
GenNext Technologies, Inc., is collaborating with Emery Pharma, a full-service CRO offering end-to-... read more »

Alcami Appoints General Manager of Biostorage and Pharmaceutical Support Services
Alcami Corporation announced the appointment of Laurent Boer to the newly created position of ... read more »

	Featured Articles

		Regulatory Operations – Enhanced Business Processes Will Fuel a Data-Driven Future There is general agreement now that the shift away from inconsistent manual, document oriented ... read more »

		Digital Knowledge Management Drives the Connected Pharma Enterprise The rapid development, manufacture and distribution of vaccines that began in early 2020 to combat ... read more »

	Featured Video

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 »

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 »

	Featured White Papers

		Whitepaper: Shaping the Future of Formulation Development with Melt-based 3D Printing Technologies In this white paper, the use of 3D printing to overcome challenges during formulation development is explored, with a focus on enhancement of ... read more »

		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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	Service Directory

Analytical Method Development Services Search More

Pharmaceutical Particle Size Analysis Services Search More

Preclinical Services and Development Search More

	Events

CRS 2023 Annual Meeting
Las Vegas, Nevada, USA – 07/24/2023
The 2023 Annual Meeting & Expo reflects our focus on cutting-edge research and innovation across our strong discipline that will keep you up-to-date ... event details »

AAPS 2023 PharmSci 360
Orlando, FL – 10/22/2023
AAPS brings together pharmaceutical scientists from around the world to share research and exchange ideas in order to improve global health. event details »

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