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February 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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» Featured Articles
The Power of Collaboration: Using the Pandemic’s United Effort to Serve as a Model for Future Drug Development
The COVID-19 pandemic has marked a pivotal moment in the healthcare system, pushing players across the full spectrum of healthcare to work together and act quickly to address a novel virus. read more »
Global Ambitions: Biotech in China
Pharmaceutical companies based in China are increasingly eyeing the international market, especially for new drug developments in the biological field. China has changed its domestic market policy and... read more »
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» Featured Partners
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  Connecting and Leveraging Quality-Driven Data Throughout the Pharmaceutical Product Life Cycle

Your ability to connect data across the product life cycle is what sets you apart in the pharma industry. Download MasterControl’s e-book to learn how advanced digital tools can help you improve product quality and stay at the front of the pack. read more »
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  A Technology Driven CDMO Delivering Integrated End-To-End Services

Adare Pharma Solutions provides CDMO services from product development through commercial manufacturing and packaging, with expertise focusing on oral dosage forms. With a proven history in drug delivery, Adare has developed and manufactures more than 45 products sold by customers worldwide. read more »
» Featured Video
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  On-Demand Webinar: Integrated Drug Product Development – Considerations from Pre-Clinical to Commercialization
In this webinar you’ll learn about capability and planning requirements for effective integrated drug product development; phase- appropriate considerations for development programs from simple to ... read more »
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  On-Demand Webinar: Optimizing Outcomes Across the Pharma Value Chain Network
The ability of bio-pharmaceutical manufacturers to deliver quality drug products during challenging market conditions is critical for ensuring sustainability over the long run. The COVID-19 pandemic ... read more »

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» Featured Whitepaper
Poster: Evaluation of Viscosity Effects on Drug Dissolution and Permeation across Caco-2 Monolayers Using In Vitro Dissolution and Absorption Systems (IDAS)
Download this poster to learn more about the determining the effect of medium viscosity on diffusion and permeation of API across Caco-2 cell ... read more »
Poster: Applications of the In Vitro Dissolution and Absorption System 2 (IDAS2) as a Bioequivalence Biowaiver Tool
In vitro comparative dissolution profiles (CDP) are widely accepted to ensure product quality and consistency and to assess bioequivalence (BE) in ... read more »
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| Events
EVENT
  SMi’s 5th Annual 3D Cell Culture Conference
Virtual –  02/09/2022
Sponsored by: CELLINK, CelVivo, Promega and Newcells Biotech   Developing Complex, Translatable and Physiologically-Relevant Cellular Models in ...
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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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