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Aseptic Processing Validation
By Ross Acucena and Randy Wilkins
Published April 4, 2012
Best practices for sterile filtration validation of re-use and extended-use processes Read More »
Published February 27, 2012
A method of producing a sterile (devoid of living organisms) product in which sterile bulk drug or raw materials are compounded and assembled with sterile packaging components.… Read More »
Aseptic Processing Update
By Hal Baseman
Published April 5, 2011
What�s new in aseptic processing, validation, and contract manufacturing? Read More »
Newsmakers: Aseptic Processing
By Gil Y. Roth
Published March 3, 2010
Q&A with PDA President Richard M. Johnson Read More »
By Laurent Veuillet, Vice President
By Ron Zagorski, Account Manager
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 »
Microbiological Environmental Monitoring
By Daniela Jansen, Ph.D., Accelrys
Published March 7, 2014
Three hurdles you need to overcome. Read More »
Vetter Pharma International GmbH
By Oskar Gold, Vice President Key Account Management & Corporate Marketing
body {font-family:arial;} .heading {color:#BA5915;font:24px arial;} Vetter is a leading contract development and manufacturing organization (CDMO) that specializes in the aseptic filling of syringes, cartridges and… Read More »
Therapure Biopharma Inc.
By Rajan Puri, Director, Business Development
Therapure Biopharma is a Contract Development and Manufacturing Organization (CDMO) that specializes in the development, scale up and manufacture of complex biologics. Therapure operates a modern 130,000 ft2 cGMP facility in the Greater Toronto Area… Read More »

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