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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 Ron Zagorski, Account Manager
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 »
By Eugen Goidenko, Director of Sales
Alkermes
By Fidelma Callanan, Sr. Director Marketing and Commercial Development
Four decades delivering contract pharma solutions for our Partners Alkermes Contract Pharma Services provid… 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 »
Published February 27, 2012
A method of producing a dry powder from a liquid or slurry by rapidly drying with a hot gas. Spray drying can be used as an encapsulation technique.… Read More »
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