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July 18, 2019
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  Solid Form Selection in Drug Development

Drug formulators should consider the physical properties of their products during pharmaceutical drug development. The physical properties of a solid drug substance are highly dependent on the solid form. It is critical to understand the solid form landscape and select the optimum solid form for drug performance, stability and manufacturability as early in the development process as possible. Join this free webinar to learn about different solid forms and different technologies to achieve these forms.

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» Industry News
 
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» Featured Articles
Oral Solid Dosage Manufacturing Roundtable
Many issues that the pharmaceutical drug development industry face not only affect oral solid dose manufacturing and one of the constant challenges is the scalability of new molecules emerging from ... read more »
HORIZON LINES: A Quarterly Review of New Drug Applications – January-March 2019
This quarterly review on New Drug Applications contain data for applications approved for the first time during the first quarter of 2019, which includes New Molecular Entities (NMEs) and new ... read more »
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» Featured Partners
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  We help our partners succeed. Reduce Risk. Improve outcomes. Free them to grow.

Whether it’s getting rid of a headache or saving a life, we help develop and test the products that improve the health of everyone in our communities and around the world. For this reason, we are committed to getting it right every time. read more »
» Featured Video
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  Watch Video: Pfanstiehl - Global Leader in Bioprocessing Solutions
Pfanstiehl specializes in isolation, purification, custom synthesis and scale-up development of regulated, high purity and low endotoxin Injectable Formulation Ingredients, Pharmaceutical ... read more »
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  The Power to Make: A Virtual Tour of Althea
Althea is a contract pharmaceutical development and manufacturing organization that supports the drug development process all the way from early-stage clinical trials through commercial manufacturing.... 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 »
Support of Scale-Up and Technical Transfer Through Understanding Equipment for Lyophilization
Formulation and process development for injectable products are typically conducted at laboratory-scale. There are few challenges when increasing the ... read more »
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| Events
EVENT
  10th Clinical Quality Oversight Forum
Philadelphia, PA –  10/16/2019
ExL’s 10th Clinical Quality Oversight Forum focuses on ensuring trial integrity by effectively assessing, optimizing and managing the quality of ...
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EVENT
  2019 BIO Investor Forum
San Francisco, CA –  10/22/2019
Join your peers from public and venture-stage growth companies, and top public and private equity investors, to explore collaborations and attract the...
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