Contrary to an industry trend ... we have stepped on the accelerator. ...we are committed to our vision of One World, One Quality generic APIs
Woodbridge, CT (PRWEB) January 08, 2016
ChemWerth, Inc., is pleased to announce that since the inception of Generic Drug User Fee Amendments (GDUFA) in 2012, the company has filed its 50th Drug Master File that the FDA has deemed as Available for Reference. The company continues to rank #1 in DMFs Available for Reference among all other peer active pharmaceutical ingredient companies.
“Contrary to an industry trend which has seen many competitors decrease their API development, we have stepped on the accelerator. We will continue to invest in specialty generic API products to support our customers around the globe, and we are committed to our vision of One World, One Quality generic APIs,” said Peter J. Werth, President and CEO, ChemWerth, Inc.
In addition to filing its 50th DMF available for reference, the company has 45 first to file APIs. Werth added, “Our customers have come to rely on ChemWerth to provide them with first to market advantage. This provides our customers with a big competitive edge and that continues to be a big reason for our success.”
About ChemWerth, Inc.
ChemWerth is a world leader in developing and supplying specialty Generic Active Pharmaceutical Ingredients for the human and animal health markets. ChemWerth is the regulatory agent for numerous FDA approved facilities in China, the United States, Europe and India. The company sells to the top generic pharmaceutical companies in the industry and sells products in 38 countries around the globe. For more information about the company please visit http://www.chemwerth.com.