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CMC Biologics Highlights Technical Acumen at Upcoming Conferences
Date:4/16/2012

5 a.m.
Title:  What is the Progress towards Harmonization of Standards and Best Practice for E&L? How Should/Does the Industry Qualify, Test, Validate, Engineer and Set Standards for Single-Use Applications?
Presenter:  Morten Munk, Vice President Business Development, Technology Specialist

Presentation Date and Time:  Tuesday, June 5, 2012 at 3:00 p.m.
Case Study:  Scale-Up Into and Implementation of a 2000 Liter Single-Use Bioreactor in an Existing cGMP Facility – Lessons Learned
Presenter:  Andy Walker, Vice President Process Development 

2012 Biotechnology Industry Organization (BIO) International Annual Convention, Boston, MA

Exhibition Dates:  June 18 – 21, 2012
CMC Biologics will be exhibiting at Booth 664 in the Bioprocessing Zone.  Stop by to learn about us and enjoy special Seattle and Copenhagen coffee, food and wines throughout the exhibit.

For questions or additional details, please contact Stacie Byars, Senior Manager Global Marketing, at sbyars@cmcbio.com.

About CMC Biologics

CMC Biologics is a leading contract development and manufacturing organization that provides fully integrated biopharmaceutical development and manufacturing solutions to clients around the world, from its facilities in Europe and the USA.  The company has proven expertise in delivering custom solutions for the scale-up and cGMP manufacture of protein-based therapeutics for pre-clinical, clinical trials and in-market production.  The company's wide range of integrated services includes cell line development, bioprocess development, formulation and comprehensive analytical testing.  Clients can also benefit from CMC Biologics' proprietary CHEF1® expression system for mammalian production.  CMC Biologi
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