Life Sciences at Nymbl
Scalable Software for Life Sciences—Built for What’s Next
We specialize in building secure, scalable software solutions for the highly regulated and rapidly advancing world of life sciences. Whether you're streamlining clinical trial workflows, digitizing lab operations, or building an AI-powered analytics platform, our technology-agnostic approach meets you where you are—and delivers the results that matter.
Nymbl delivers life sciences software that accelerates research, enhances compliance, and empowers breatkthroughs.
Life science organizations come to Nymbl when they’re facing...
Siloed systems across R&D, clinical, and regulatory teams
Manual processes slowing down drug discovery or trial operations
Difficulty meeting complex compliance standards like FDA 21 CFR Part 11
Inefficient lab workflows and fragmented data tracking
Inconsistent patient or site onboarding experiences
Limited real-time insights into study progress or research data
Rising costs of maintaining outdated LIMS, CTMS, or QMS platforms
Rising costs of maintaining outdated LIMS, CTMS, or QMS platforms
Science moves fast—we make sure your systems can keep up. We custom build it for you.
At Nymbl we collaborate with
Our mission is to build life sciences platforms that accelerate time to discovery, improve collaboration, and ensure compliance—without compromising scientific integrity.
Yesterday’s Systems Can’t Power Tomorrow’s Breakthroughs
Today’s life sciences platforms must deliver compliance, agility, and transparency across every research stage and business function.
But many organizations are still held back by:
- Legacy LIMS or CTMS systems that limit collaboration and scale
- Manual data capture in labs, clinics, or studies
- Paper-based SOPs and documentation slowing compliance reviews
- Disconnected patient or investigator portals
- Inflexible platforms that don’t support evolving study designs
- Gaps in audit trails and validation documentation
- Clunky, outdated UIs frustrating teams and slowing workflows
- Isolated datasets across departments and vendors
You know change is needed. You’re deciding how. Whether you're...
Digitizing paper-based lab or clinical processes
Automating compliance documentation or regulatory workflows
Building a modern CTMS or LIMS to support new study models
Launching a patient engagement or investigator portal
Unifying data systems across R&D, regulatory, and quality teams
Integrating with EDC, ePRO, or third-party lab systems
Creating dashboards for real-time study progress and site metrics
Migrating from legacy infrastructure to a modern cloud platform
Developing a digital health or SaMD product
Exploring AI for trial matching, molecule modeling, or data monitoring
We Roadmap and Custom Build for You.
Our development team specializes in...
FDA 21 CFR Part 11 and HIPAA-compliant digital transformation
Custom CTMS, LIMS, QMS, and eTMF platform development
Clinical trial automation and patient/site workflow tools
Laboratory information and sample tracking systems
Real-time dashboards for study metrics and operational insights
Regulatory submission management and audit trail tools
Patient portals and remote monitoring solutions
AI-powered analytics for study optimization and research insights
Coordinating care across multiple providers and facilities
“Nymbl helped us build a compliant, scalable CTMS that cut study setup time by over 40%—and gave us better visibility into trial performance.”
– VP, Clinical Operations
We Make Change Real
—And Achievable.
Digital transformation in life sciences demands more than feature-rich software. It requires:
End-to-end data integrity and validation
Deep compliance expertise across regulatory frameworks
A development partner who understands scientific complexity
Our agile approach balances rapid delivery with rigorous compliance alignment. We focus on...
MVPs that deliver fasttime-to-impact
Compliance with HIPAA, GxP, 21 CFR Part 11, and EU Annex 11
Seamless integration with your systems, labs, and third-party tools
Collaboration with your science, regulatory, and operations teams
Why Nymbl for Life Sciences
Software Development?
Proven experience
75+ digital solutions delivered across biotech, medtech, and clinical research—supporting everything from early-stage R&D to post-market surveillance.
Deep expertise
Integrated with over 35+ regulated systems, including ELNs, LIMS, CTMS, and QMS platforms—ensuring data integrity and compliance.
Legacy tools to scalable platforms
Modernized legacy tools into scalable, audit-ready platforms—helping clients reduce validation time by up to 40%.
Agile model
Agile development with MVPs deployed in as little as 12–16 weeks and ongoing iteration aligned to clinical and scientific workflows.
Trusted Partner
A long-term partner with a 95%+ client satisfaction rate—trusted to build high-quality, GxP-compliant software for global life sciences teams.
Our Services
Let’s Build What Life Science Needs Next
No more fragmented systems. No more compliance gaps. Just secure, intelligent life sciences software built to support discovery, development, and delivery.