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Pharmaceutical Sciences, Manufacturing & Marketplace Report March 27, 2013


  From Cynthia Challener, PhD, Editor, Pharmaceutical Sciences, Manufacturing & Marketplace Report
Welcome to the third edition of the Pharmaceutical Sciences, Manufacturing & Marketplace Report, a new biweekly newsletter of Pharmaceutical Technology and BioPharm International, and an exclusive feature of the new Pharmaceutical Technology/BioPharm International Marketplace, an online community focused on products and services for drug development and manufacturing, which will launch in April 2013. The Pharmaceutical Sciences, Manufacturing & Marketplace Report provides insight in five main communities: solid dosage, semisolid, and specialty dosage forms; parenterals; chemical API manufacturing; biologic API manufacturing; and pharmaceutical analysis.

In this issue, we are looking forward to Interphex next month with our lead story on advances in continuous tableting equipment. You can also read about perspectives on chemocatalysis for asymmetric synthesis from catalyst manufacturers and end users, learn about the latest issues regarding the filtration of parenterals, find out why SAFC introduced its new PharmaGrade raw materials for biopharmaceutical applications, and see how rapid, automated microbiological analysis can have a positive impact on production operations.
 		 
 

       
       
Solid, Semisolid, and Specialty Dosage Forms
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Ion-Bogdan Dumitrescu/Getty Images
Making Strides in Continuous Tableting

Equipment suppliers are helping the pharmaceutical industry move towards adoption of continuous tablet production. Click Here to Read More
Join our Solid, Semisolid, and Specialty Dosage Forms Linked-In Community
 
Chemical API Manufacturing
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Alfred Pasieka/Getty Images

Asymmetric Chemocatalysis: Going for the Lowest Loadings

Although the use of biocatalysis for asymmetric transformations is growing, chemocatalysis remains a highly competitive technology.Click Here to Read More
Join our Chemical API Manufacturing Linked-In Community
 
Parenterals
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Maciej Frolow/Getty Images

Filtration Critical Issue for Parenterals

Russell Madsen, group leader of the Parenteral Drug Association (PDA) Filtration Interest Group, discusses technical and regulatory considerations in filtration for parenteral drug manufacturing. Click Here to Read More

Join our Parentals Linked–In Community
 
Biological API Manufacturing
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Adam Gault/Getty Images

Strategies for Achieving Biopharmaceutical Supply-Chain Security

Ensuring the quality of raw materials is a crucial component of achieving product quality of APIs and finished drug products. Click Here to Read More

Join our Biological API Manufacturing Linked-In Community
 
Pharmaceutical Analysis
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Maria Toutoudaki/Getty Images

Advances in Rapid Microbiological Testing

It can take up to two weeks or more to obtain results from traditional microbiological testing methods. Rapid, automated testing can reduce that time in half. Click Here to Read More
Join our Pharmaceutical Analysis Linked-In Community
 
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Perspectives from Cynthia Challener, PhD, editor of the Pharmaceutical Sciences, Manufacturing & Marketplace Report and industry members

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