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Published March 1, 2011
Contract Pharma Editorial Staff Editor Tim Wright Editorial Director Tom Branna Associate Editor Kristin Brooks Editor at Large Tom Spurge… Read More »
Published February 28, 2011
Contract Pharma and ContractPharma.com are leaders in coverage of the Pharma outsourcing industry. ContractPharma.com is quickly becoming one of the most visited sites on the Internet for pharma and biopharma decision-makers looking for th… Read More »
News
Published February 28, 2011
Find the latest news and trends related to outsourcing and contract services for pharma and biopharma by clicking on specific news categories below. Read More »
Contract Pharma Team
Published February 28, 2011
Contract Pharma Team President, Rodman J. Zilenziger, Jr. Rodman J. Zilenziger Jr. — President of Rodman Media since 1993. Zilenziger, son of the Company’s founder, joined Rodman Media as an Advertising Representa… Read More »
By Brigitte de Lima, Results Healthcare
Published November 13, 2014
Pharma suppliers need to adapt to support innovation. Read More »
LSNE Contract Manufacturing
By Christine Palus, VP of Sales and Marketing
LSNE Contract Manufacturing is a privately held company with facilities located in Bedford and Manchester, NH. LSNE has been providing lyophilization services to the pharmaceutical, biotechnology and medical device industries since 1997- specializing… Read More »
By Kristin Brooks, Associate Editor
Published March 10, 2014
Agnes Shanley brings 24 years of editorial and publishing expertise Read More »
Chartwell Pharmaceuticals, LLC
By Jack Monoker, VP Business Development
Chartwell Pharmaceuticals is a full-service contract manufacturing and packaging organization located in the heart of suburban New York. For over twenty years, quality pharmaceutical products have been produced in our 40,000-sq.-ft., state-of-the-art… Read More »
Published February 27, 2012
Issued by the U.S. FDA when communicating a decision to a drug company that an NDA or ANDA to market a new or generic drug will not be approved in its present form. Before August 2008, the FDA used Approvable and Not Approvable letters in these cases… Read More »
Published February 27, 2012
An FDA-approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the RLD in its ANDA. By designating a single RLD as the standard… Read More »


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