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EMPROVE® bio for use in biopharmaceutical production

Raw material qualification is a key factor in assuring the quality and safety of biopharmaceuticals. Even still, performing tests and compiling required documentation on your own is costly and time-consuming. That’s why we’ve developed EMPROVE® bio raw materials – your solution for getting products to market faster.

Reliable, ready-to-use documentation

Our EMPROVE® bio raw materials for use in biopharmaceutical production offer specifications adapted for use in upstream or downstream process steps. These dossiers contain comprehensive data on the manufacturing processes, testing procedures and purity. Select EMPROVE® bio products also comply with ACS standards.

With EMPROVE® bio, you benefit from Merck Millipore’s known expertise and reputation for uncompromising reliability and safety. As a result, you can considerably accelerate your qualification, helping you to reduce your workload and costs.

Features of the EMPROVE® bio portfolio:

Analytical Dossier
(Basic Dossier+Analytical Method)

  • CDA necessary
  • Charged
  • In line with CTD format

Basic Dossier

  • Available online
  • Free of charge

Specification adapted to biopharmeceutical production process

  • Endotoxins: tested (partly)
  • Microbiology: tested (partly)
  • Proteases: tested (partly)
  • ACS reagent standard: tested (partly)
  • In line with CTD format

Click here for a comprehensive list of EMPROVE® bio products.

For more information on all EMPROVE® dossiers, please click here.

© Merck KGaA, Darmstadt, Germany, 2014


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