Compounding for a new generation of care

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What we do
We deliver personalized medicine at enterprise
scale. That means we're the partner of choice for fast moving telehealth.
our operating system
Sterile and non-sterile compounding done right
From intake to fulfillment, we run a modern compounding operation engineered for consistent outcomes — clean handoffs, clear documentation, and a production model that scales as your patient volume grows. Whether you need sterile preparations, non‑sterile formulations, or both, you get one partner with a process designed to reduce friction and protect quality.
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503A
Our 503A operations support personalized therapy without sacrificing operational discipline — ensuring prescriptions are compounded accurately, efficiently, and responsibly.
503B Outsourcing
Our 503B operations help partners expand access to compounded medications while maintaining trust, transparency, and operational control.
Our Advantage

Built to scale. Built to trust.

We’ve built our operation for consistency, transparency, and partnership — so providers and telehealth teams can move fast without compromising confidence.
10,000,00+
Doses of personalized capacity anually
87%
→
Reduction in operational risks
100%
→
Transparency in project reporting
superior capability

Full white labeling to elevate your practice

We enable practices and care organizations to offer compounded medications under their own brand, without operational burden. Our white-label approach prioritizes consistency, discretion, and clear coordination across both 503A and 503B workflows.
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Client Story
Modulabs helped us from construction blueprints to digital templates
Jessica Mercedes
Marketing
FAQ
Questions, answered with clarity
Do you offer both 503A and 503B compounding?

Yes. We support both 503A patient-specific compounding and 503B outsourcing services, allowing partners to choose the model that best fits their clinical and operational needs.

How do you approach quality and compliance?

Both our 503A and 503B operations are abide by full cGMP requirements and are built around defined controls, documented processes, and disciplined execution. We emphasize consistency, traceability, and accountability across all compounding activities.

How do new partners get started?

Getting started begins with a conversation to understand your needs, workflows, and regulatory requirements. From there, we align on the appropriate compounding model and next steps.

Can you support growing or evolving programs?

Yes. We work with partners at different stages, from early program development to more established care models, and adapt our support as requirements change.

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