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October 04, 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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  Almac Group Announces New COO and Appoints New Almac Pharma Services MD
The Almac Group announced the appointment of Graeme McBurney to the Board of Directors in the role ... read more »
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  Samsung Biologics introduces New Development Platforms S-DUAL and DEVELOPICK at BPI Boston 2022
Samsung Biologics, a world-leading contract development and manufacturing organization (CDMO), is ... read more »
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  Quotient Sciences Expands Capabilities at Two UK Sites
Quotient Sciences, a drug development and manufacturing accelerator, completed major investments and... read more »
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  Lykan Bioscience Appoints Ressler as VP Manufacturing Process Sciences
Lykan Bioscience named Barbara Ressler, Ph.D. VP of Manufacturing Process Sciences. development, ... read more »

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» Featured Articles
EVENT   Three Ways Pharmaceutical Manufacturers Can Benefit from NIR Technology
For pharmaceutical manufacturers, measuring and controlling moisture content is critical to ensure product safety, quality and efficient production since the amount of moisture in deliverables can ... read more »
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 the long-term preservation of biospecimens such as tissue, blood, plasma, or urine. These ... read more »
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» 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 Pitfalls and Strategies for Pediatric Formulation Development
In this webinar you’ll learn common issues and strategies for pediatric formulations development as well as some of the various resources and regulatory bodies; Impact of age group, daily dose, and ... 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: 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 »
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» More Services
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| Events
EVENT
  SAE Media Group’s 2nd Annual Biosensors for Medical Wearables
Boston, MA –  10/24/2022
Advances in development and therapeutic applications of on-body sensors SAE Media Group is proud to present the Biosensors for Medical Wearables ...
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EVENT
  PDA Pharmaceutical Microbiology Conference
Washington, DC –  10/10/2022
The 2022 PDA Pharmaceutical Microbiology Conference continues the ongoing tradition of addressing the most relevant opportunities and challenges to ...
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