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Emprove
Your fast track through regulatory challenges

The New Emprove® Program
 
Products and dossiers to support your processes
Read more about the Program

  • Emprove Program | Merck

    Your fast track through regulatory challenges With the industry facing ever increasing regulations for risk assessment, we've broadened the scope of our Emprove® portfolio and dossier structure to help you meet the latest regulatory requirements and speed your way through the regulatory maze.

  • Emprove Program | Merck

    Your fast track through regulatory challenges With the industry facing ever increasing regulations for risk assessment, we've broadened the scope of our Emprove® portfolio and dossier structure to help you meet the latest regulatory requirements and speed your way through the regulatory maze.

  • Emprove® Suite Subscription | Merck

    Getting the relevant information is now more convenient than ever: besides buying single dossiers, you can use the new Emprove® Suite online to find all our Emprove® Dossiers.

  • Emprove® Evolve For Raw Materials | Merck

    Emprove® Evolve For Raw Materials: Used in Early Stages of Biopharmaceutical Manufacturing. The new Emprove® Evolve product line provides fit-for-purpose high-quality raw materials addressing applications in early stages of pharmaceutical and biopharmaceutical manufacturing such as: upstream processing, early downstream processing, clean-in-place, early synthetic steps in small molecule drug manufacture.

  • Emprove® Extractables Data for Filters and Single-use Systems | Merck

    Enabling a More Robust Extractables and Leachables Risk Assessment extractables and potential leachables. All polymeric components such as the filters and single-use systems used in biopharmaceutical manufacturing must be assessed for safety through an evaluation of extractables and potential leachables. Extractables are compounds that can be extracted from these materials while leachables are compounds that leach from the materials into the process stream.

  • Emprove® Chromatography | Merck

    Emprove® Dossiers for Purification in Biomanufacturing Process High performing resins meet regulatory excellence 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.