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MODA® – GMP Manufacturing & Quality Software

The MODA® Platform combines manufacturing and laboratory data into a single comprehensive source to expedite pharmaceutical product release. Leveraging Moda’s expertise in manufacturing and quality the solution enables organizations to achieve paperless execution and remove manual, error prone workflows.

The platform is user centric, modular, and scalable.

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The MODA® Platform: Digitalize quality and manufacturing

The MODA® Platform is comprised of 3 modules. Choose the module that’s right for you and easily scale to suit your requirements by adding additional modules when necessary.

  • MODA-EM® Quality Control – Automating the full spectrum of QC activities
  • MODA-ES® Manufacturing – Intuitive, flexible and proof with efficient electronic batch records
  • MODA® eLogs Electronic Logs – User-friendly, compliance-enforcing electronic logs

Why choose the MODA® Platform?

The MODA® Platform is designed specifically for the pharmaceutical industry to enable organizations to digitalize their operations.

A track record of success

We have extensive experience in pharmaceutical manufacturing and informatics, having worked with customers around the world, across all therapeutic modalities. Partnering with us gives you the expertise needed for timely implementation and long-term digitalization success.

Our industry experience

The MODA® Platform addresses the issue of paper records associated with batch records, QC forms and logbooks, long cycle times for review/approval activities, deviations for missing entries, incorrect entries, calculation errors.

Moda looked externally for a solution, but found the marketplace was too expensive and not flexible enough to meet our needs for clinical phase CMO customers that had changes more frequently than commercial applications.

The Moda Informatics Team stepped in to help solve that issue. The combination of the subject matter expertise from multiple Moda Manufacturing Groups and Moda Informatics understanding of paperless solutions, is a regulated object allowed for a product that serves the needs of the mid-sized CMO/Pharma plant. Moda Informatics know how and Moda manufacturing’s experience allowed for a more flexible, cost-effective solution to replace paper records than other solutions in the market.

What our customers say

Rather than also installing a LIMS, we made the decision to install the MODA-EM® Module only. Not only did it mean not having to invest in a second system, we also didn’t have the duplication of tasks and effort that might otherwise have been required.

– Nikon CoE, Innovation Co.

It’s a tremendous value… it actually gives you a significant competitive advantage, there is no question about it. For us, we value speed, and this is a must. We would spend sometimes [on the paper] weeks trying to reconcile the batch records and release it, and a lot of it was wasted time. So, there was no question, it has to be done.

– Dr. Phanesh Koneru, CEO of Exela Pharma Sciences

Related resources

White paper
Globally deploying digital pharmaceutical manufacturing and quality tools
Key takeaways shared during the 2024 Annual MODA User Group Meeting that are actionable, vetted by industry leaders who have deployed software globally, and can help you smoothen out the path to a successful global deployment.

Learn more

How-to guide
Key steps for planning the integration of a fit-for-purpose MES
Learn about the key role of manufacturing execution systems (MES) and digital environmental monitoring tools, and how to select the most appropriate options for your needs.

Get the guide

Webinar
Building processes for modularity and scalability in a GMP environment
Watch this webinar with Nick Penwell, Principal MES Implementation Engineer at KB Biopharmacy and learn how traditional, siloed processes can be strategically streamlined to create re-usable, digital processes that enable efficient scalability across multiple processes.

View webinar