Need help with Life Sciences Software Development?
Whether you're developing a new digital health product or extending an existing solution with Life Sciences Software Development, 6B brings the technical expertise, healthcare insight, and experience needed to accelerate delivery.
From lab automation and clinical trial management to bioinformatics, data platforms, and regulatory systems, we deliver software built to handle complex data, streamline workflows, and ensure compliance with global standards. Whether you’re in early-stage research or scaling to market, 6B provides the technical expertise and domain understanding needed to support every step of your digital journey.
Understanding Life Sciences Software
Software plays a critical role in the development and delivery of life sciences innovations. Whether supporting molecular research, drug discovery, clinical trials, or regulatory processes, these systems must be precise, traceable, secure, and aligned with scientific and regulatory expectations.
Common use cases include:
- Laboratory Information Management Systems (LIMS)
- Electronic Lab Notebooks (ELN)
- Clinical Trial Management Systems (CTMS)
- Regulatory submission and documentation tools
- Data analytics and bioinformatics platforms
- Workflow automation and sample tracking
- Integration with instruments, EDC, and compliance frameworks
Life sciences software must meet high standards for data accuracy, auditability, and compliance — including GxP, FDA 21 CFR Part 11, ISO 13485, and GDPR. At 6B, we design platforms that align with these standards from the outset, enabling safer, smarter innovation.
Our Life Sciences Software Development Process
As an experienced Life Sciences Software Development company, we provide end-to-end services that span research, development, and regulatory delivery.
We begin by understanding your scientific goals, operational models, and compliance requirements. Through discovery workshops and stakeholder engagement, we define your functional requirements, data models, and system architecture — whether you’re digitising lab processes, managing trial data, or automating submissions.
Our development process is agile, collaborative, and quality-driven. We build secure, scalable systems using modern cloud-native technologies and open standards. Validation, traceability, and documentation are embedded throughout, ensuring full alignment with GxP, FDA, EMA, and MHRA expectations.
We support system validation, integration with lab instruments, and post-deployment enhancements — ensuring your platform delivers long-term scientific and commercial value.
Benefits of Custom Life Sciences Software
Investing in tailored life sciences software delivers critical advantages across research, development, and compliance.
Scientific teams benefit from automation, structured data capture, and collaboration tools that reduce time to insight and improve reproducibility. Project teams gain real-time visibility into progress, performance, and risk — whether in early R&D or multi-phase clinical trials.
Organisations see improved regulatory readiness, with audit trails, digital signatures, and validated systems that meet global submission standards. Custom platforms also offer long-term adaptability — allowing you to evolve workflows, add integrations, and stay ahead of changing standards.
At every stage, 6B delivers software that drives speed, compliance, and innovation.
