The Emprove® Program

Your fast track through regulatory challenges

With the industry facing ever increasing regulations, our Emprove® Program helps you meet the latest regulatory requirements for risk assessment and speed your way through the regulatory maze.The Emprove® program simplifies your processes by:

Expediting approval preparation
and extending compliance Emprove® dossiers accelerate your preparation of the drug approval process with professionally prepared documentation that goes beyond regulatory requirements. In addition to our customer support and 24/7 online document access, the dossiers provide the information you need, speeding up internal qualification procedures.
Facilitating qualification processes
In order to facilitate your qualification process, we offer information on fundamental properties of our products, such as manufacturing procedure and stability.
Supporting risk assessment,
management and mitigation We support our partners in their risk assessment efforts by providing detailed information about the applied Quality Management system, the supply chain, and data on the stability of a product.
Increasing supply chain
transparency Our Quality Management Dossier provides detailed supply chain information summarizing the chain of custody during manufacturing, filling, labeling, testing, and release of material.
Saving you time and money
Our Emprove® Program allows you to reduce the time, effort, and resources needed for document preparation. You don’t have to develop test methods in-house, search quality-related documents, or evaluate scientific data yourself. Instead, focus on what’s most important: innovating new drugs.
Merck
Discover the benefits of the Emprove® Program
Merck
How Emprove® Dossiers for Chemicals can support you
Merck
How Emprove® Dossiers for Filters and Single-use Components can support you

What is the Emprove® Program?

The Emprove® Program supports your risk assessment and offers assistance in developing more robust processes. It also provides comprehensive and thorough documentation of our filters and single-use components as well as pharma raw and starting materials. It not only covers the latest regulatory requirements, but also anticipates industry expectations not yet covered by regulation.

More about the Emprove® Dossier Library

Emprove® Portfolio

To help you optimize your process, our Emprove® portfolio spans approximately 400 raw and starting materials as well as a selection of filters, single-use devices and components.

Emprove® Chemicals Emprove® Filters and Single-use Components

Emprove® Dossiers

The Emprove® Program is organized in three different types of dossiers. Every dossier supports you throughout different stages of your operations: qualification, risk assessment, and optimization.

Emprove® Dossier Library for Raw and Starting Materials Emprove® Dossier Library for Filtration and Single-use Components Emprove® Suite for 24/7 Access to All Emprove® Dossiers Online

Stay Connected

We are committed to keeping you informed on updates to our Emprove® Program, new guidelines, and related regulatory topics.

Knowledgebase & Tools

Regulatory Sources

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Start Your Emprove® Suite Subscription Today

Getting the relevant information is now more convenient than ever: in addition to buying single dossiers, you can use the new Emprove® Suite online to find all our Emprove® dossiers. The Suite is constantly updated and is optimized for targeted search. All our subscribers to the Emprove® Suite get online access to all dossiers of the entire Emprove® portfolio for two years.

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