Weave

Weave

From preclinical to postmarket, Weave guides therapeutic development through the regulatory journey.

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Industry
IT System Custom Software Development
Company size
60 people
Headquarters
San Francisco, CA +7 more
Founded
2023
Type
Privately Held
Total funding
$43.0M

At Weave Bio, we’re building the backbone for modern drug development. Drug development teams deserve tools that match the pace and complexity of their science. Our AI-native platform supports biotech and pharma organizations at every step, with a focus on regulatory workflows that bring clarity, connection, and efficiency to documentation so therapies can move forward without unnecessary delays. We partner with scientists, clinicians, and regulatory professionals who are advancing the next generation of medicines. By improving the processes behind regulatory documentation, Weave helps reduce bottlenecks and frees teams to focus on what matters most — discovery, innovation, and patient impact. Our approach is human-driven and technology-powered. We believe that combining scientific expertise with AI innovation can transform how life sciences organizations operate, making the development of therapies more efficient, compliant, and collaborative. Weave is a small but mighty team of scientists, engineers, and industry experts united by a shared mission: helping life-changing medicines reach patients faster. Our collective experience across biotechnology, software, and regulation gives us deep insight into the challenges of drug development — and the passion to build solutions that make a lasting impact. We’re proud to work side by side with our partners to move science forward and build the foundation that drug development teams need today and tomorrow.

Regulatory document automation Regulatory document preparation Preclinical Document Authoring Clinical Protocol Development IND Authoring Investigator’s Brochure (IB) Preparation Clinical Study Report (CSR) Automation Regulatory Strategy Alignment AI-Assisted Medical Writing eCTD-Ready Document Formatting Clinical & Regulatory Lifecycle Global Submission Readiness

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