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March 05, 2020
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  Whitepaper: Advancing API Development

As drug products become more sophisticated, so does the process of active pharmaceutical ingredient (API) sterilization. The sources of contamination are multiple – all posing the risk of microbial and particle intrusion, which can have negative consequences for the health of both patients and your business. Success relies on industry-leading expertise, careful planning, flawless processes and state-of-the-art equipment and facilities. Access our free white paper to learn more!

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» Industry News
 
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» Featured Articles
HORIZON LINES: A Quarterly Review of NDAs –July-September 2019
This quarterly review of new drug applications contain data for applications approved for the first time during the third quarter of 2019 which includes New Molecular Entities (NMEs) and new biologics... read more »
Screening and Formulating Drugs as Salts to Improve API Performance
There are many reasons why it might be desirable to create a drug formulation using the salt form of an active pharmaceutical ingredient (API). Most commonly, it is because the solid-state properties ... read more »
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» Featured Partners
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  The CDMO Market: A Strategic View
In this article, Frédéric Gaussens, Vice President Business Development & Strategy, Eurofins CDMO Europe (Amatsigroup SAS), details why CDMOs are a good investment value. The aim of this article is to help clients and investors to better understand what makes a difference so as to better filter their future partner selection. read more »
» Featured Video
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  On-Demand Webinar: Formulating to Enable High Concentration mAb Stability
Live Webinar: Formulating to Enable High Concentration mAb Stability read more »
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  On-Demand Webinar: Data Integrity Practices in the Contract Laboratory Environment
Watch Live Webinar: Data Integrity Practices in the Contract Laboratory Environment read more »

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» Featured Whitepaper
eBook: Pharmaceutical Synthesis & Specialty Ingredients
This eBook takes a detailed look at the issues that affect the pharmaceutical manufacturing industry. read more »
Process Development for Lyophilized Products
Identifying the failure points for a product is a necessary part of product development, and enables the development scientist to design a ... read more »
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| Events
EVENT
  DCAT Week ‘20
New York City, NY –  03/23/2020
DCAT Week is the premier business development event for companies engaged in pharmaceutical development and manufacturing and related industries. It ...
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EVENT
  INTERPHEX 2020
New York, NY –  07/15/2020
For 41 years, INTERPHEX has proven to be the place to find all of the State-of-the-Art Solutions you need to Cost Effectively Develop and Manufacture ...
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