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Cloud compliance solutions for every stage of your journey.

Where is your company in its journey?

Getting Started

pre IND

You have to know where you are to know where you are going. We can help identify gaps, minimize risk, and fast-track getting where you want to be.

Getting Better

phase 1

We can help you maximize the return on your technology investments, increase your cloud compliance maturity, and speed up GxP projects.

Getting Ahead

phase 2 and 3

You have to know where you are to know where you are going. We can help identify gaps, minimize risk, and fast-track getting where you want to be.

How we can help:

  • Provide regulatory training and guidance to improve internal know-how

  • Establish quality and compliance best practices to minimize risk

  • Ensure compliance and audit readiness to pass regulatory audits and speed time to market

  • Define a compliant, IT roadmap based on regulatory milestones to maximize ROI

How we can help:

  • Provide a free assessment to identify compliance and technology improvements

  • Optimize technology to harmonize GxP and non-GxP functionality to save money and minimize system duplication

  • Maintain continuous compliance of your GxP tech stack to decrease internal validation workload and increase team capacity

How we can help:

  • Digitize and automate compliant processes and workflows to work faster and minimize human errors

  • Extract more value from your data to activate new business models

  • Empower data-driven decisions with AI and ML to innovate faster

  • Scale new, agile business capabilities
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Case Study

USDM helped a pre-commercial biotech establish a risk-based, phase-appropriate, CSV program and validated various application in less than 6 weeks to meet their FDA submission deadline.

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Case Study

USDM helped a pre-commercial biotech establish a risk-based, phase-appropriate, CSV program and validated various application in less than 6 weeks to meet their FDA submission deadline.

People-in-a-Office-V2

Case Study

USDM helped a pre-commercial biotech establish a risk-based, phase-appropriate, CSV program and validated various application in less than 6 weeks to meet their FDA submission deadline.

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Talk to the Experts and start your Compliance Journey.

This on-demand webinar addresses critical functional areas and drivers that impact your IT roadmap.

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