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Val@M™ Application for Validation Activities in Pharma QC Labs

The Val@M™ Application provides technology to help fulfill the requirement to keep electronic records of your validation activities around our QC platforms for microbial contamination testing. Watch the videos to learn more about our ready-to-use electronic validation protocols and what the experience of using the Val@M™ Application could look like for you.

Discover our Val@MTM application for Validation Activites

Experience the journey of using our Val@MTM application


From initial qualification of hardware and related consumables to periodic requalification and reliable method validation, we provide you with digital protocols and associated on-site services. Our validation experts have created comprehensive e-protocols to both fulfill your regulatory requirements and streamline your validation processes. They come on-site to execute the validation workflow for you through online editing and processing features directly on our e-documentation platform called the Val@M™ Application. Benefit from:

  • 21 CFR part 11 compliance
  • Real-time protocol revisions anytime, anywhere
  • Faster approval processes before and after actual usage
  • Improved data integrity and auditability
  • Several users at the same time for a protocol

To learn more about our qualification and method development validation services please visit our dedicated webpage.


Flyer: Key benefits of our Val@M™ Application
Flyer: Key benefits of our Val@M™ Application

Get an overview of key benefits of our on-line validation platform.

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Brochure: A deeper understanding of our Val@M™ Application
Brochure: A deeper understanding of our Val@M™ Application

Get more detailed information on our Val@M™ platform and learn how a fully digital validation workflow is performed.

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What is the Val@M™ Application?

The Val@M™ Application is a digital validation platform compliant with 21 CFR part 11 regulation. This cloud-based technology supports all requirements for electronic records. It is dedicated to validation activities such as Installation Qualification, Operational Qualification, Performance Qualification, and Periodic Requalification of Merck microbiology testing equipment, associated media and consumables.

How has it been validated? The Val@M™ Application is hosted on a qualified cloud-based infrastructure following Merck processes. The intended use of this technology is to execute at customer site an electronic validation protocol by a fully trained and qualified Merck validation engineer. A White Paper is available on demand for further details.

You must place a purchase order for one or more of the services offered by Merck using the Val@M™ Application. You will be guided by a Merck validation engineer to fill out an information form with relevant information on the site, user(s), and piece(s) of equipment. Merck will set them up in the Val@M™ Application. Each created user will receive an e-mail notification to activate the account and set-up your own password.

To receive a quotation for a digital protocol and associated on-site IQ & OQ service please contact your local sales representative.


We are more than happy to assist you and provide you with further information about our digital solution for validation protocol in your QC microbiology labs. Simply fill out and submit the form below .

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