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September 29, 2022
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  Choose the Optimal Oral Dosage Form for Your Drug Product

The selection of the dosage form is a key step in your drug development process. It will impact patient compliance, stability of your drug product and thus the success of your clinical study.

Eurofins CDMO supports the development, manufacturing and packaging of an optimal non-sterile oral dosage form for your drug product: Tablets, bilayer tablets, minitablets, coated tablets, Capsules, Powders, beads, granules, Gels, Solutions & suspensions.


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» Industry News
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  AbCellera Launches Second Phase of Global HQ Expansion to Advance New Medicines
AbCellera launched the second phase of its global headquarters expansion by breaking ground on its ... read more »
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  Peli BioThermal Opens New Service Center in Japan
Peli BioThermal extends service centers in Japan with a new facility, situated near Tokyo’s ... read more »
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  Kaléo Receives First DoD Contract for Ultra-Potent Weaponized Opioid Rapid Countermeasure Antidote
Kaléo announced the execution of the first contract with the U.S. Department of Defense (DoD) for ... read more »
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  Catalent Acquires Metrics Contract Services for $475 Million
Catalent, a leader in enabling biopharma, cell, gene, and consumer health partners to optimize the ... 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 the long-term preservation of biospecimens such as tissue, blood, plasma, or urine. These ... read more »
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 »
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» Featured Partners
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  Explore M Lab™ Collaboration Centers

Connect with our experts to troubleshoot existing processes and guidance for process development. read more »
» 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: 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: 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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» Service Directory
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| Events
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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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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