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Emprove® Program > Emprove® Chromatography

Emprove® Chromatography

High performing resins meet regulatory excellence


Emprove® Dossiers for Purification in Biomanufacturing Process

Emprove® Dossiers for Purification
in Biomanufacturing Process

Any component and raw material used at a later stage of the biomanufacturing process is considered a risk, as it could add a bioburden to the final drug product.

While being essential, chromatography steps are often a challenge as they are highly process specific and might be present from early to late downstream. Therefore, information is crucial for manufacturers when selecting chromatography methods and products.

Our new category Emprove® Chromatography addresses the specific needs when selecting and qualifying our chromatography resins.

Emprove® Dossiers Content

Emprove - Material Qualification Dossier

Material Qualification Dossier

Speeds up resin qualification and supports regulatory filing preparation. It includes content on manufacturing processes, product characterization, regulatory certificates, storage and shelf life information, and more.

  • General information
  • Manufacture
  • Quality information
  • Specification, release criteria
  • Packaging material
  • Regulatory statements (BSE/TSE, Allergens…)
  • Storage and shelf life
  • Environmental statement

Free of charge*

* The Material Qualification Dossier is free of charge and available on the specific product detail pages of our website after log-in. It can also be downloaded through the Emprove® Suite.

Emprove - Quality Management Dossier

Quality Management Dossier

Supports quality risk assessment by offering extended information on quality management system, supply chain, supplier and process evaluation statement, as well as stability data.

Demo Dossier

  • Supply chain information
  • Product quality self assessment
  • Supplier and process evaluation statement

Free of charge*

Emprove - Operational Excellence Dossier

Operational Excellence Dossier

Supports process optimization efforts as well as extended and safety risk assessment. It contains extractables profiles aligned with current draft** of USP<665>. It also includes information on elemental impurities, residual solvents, product quality reports and analytical procedures.

Demo Dossier

  • Manufacturing process (detailed information)
  • Elemental impurity information
  • Residual solvents statement
  • Extractables profile
  • Reference spectrum
  • Product quality report
  • Analytical procedure
  • Stability data


** Status May 2020

Emprove® Suite Subscription

Unlock Full Access to all dossiers today with the Emprove® Suite Subscription.


Products in scope

ProductCatalog NumberMaterial Qualification DossierQuality Management DossierOperational Excellence Dossier
Eshmuno® A 120089
Eshmuno® CMX 120650
Eshmuno® CPX 120083
Eshmuno® CP-FT 120093 TBD
Eshmuno® HCX 120087
Eshmuno® Q 120079
Eshmuno® S 120078
Fractogel® EMD COO (M) 116886
Fractogel® EMD DEAE (M) 116883
Fractogel® EMD DMAE (M) 116884
Fractogel® EMD SE Hicap (M) 114894
Fractogel® EMD SO3 (M) 116882
Fractogel® EMD SO3 (S) 116890
Fractogel® EMD TMAE (M) 116881
Fractogel® EMD TMAE (S) 116887
Fractogel® EMD TMAE Hicap (M) 110316
Fractogel® EMD TMAE Medcap (M) 116885
Fractogel® EMD BioSEC (S) 110317 TBD
Fractogel® EMD Chelate (M) 110338 TBD