Regulatory has one home.
It's where our AI-native software meets your human expertise.
Regulatory documents aren’t just paperwork—they’re the living record of a drug’s journey. They tell the story of a therapeutic candidate’s rise or fall. And behind every page, there’s a team of experts navigating tight deadlines, scientific complexity, and relentless organizational pressure.
Weave’s platform doesn’t just help you keep up—it puts you in control. It equips every person involved in the document preparation process with the tools to work at lightning speed, make smarter decisions, and proactively address submission risks before they arise.
Biotech
Accelerate your time to market and milestones
In the competitive world of start ups and small biotechs, efficiency isn’t just a luxury—it’s a survival strategy. Weave gives you the power to do more with less, automating the regulatory processes that would normally slow you down. With a centralized data room to ingest all your studies and files, intelligent gap analysis tools, and AI-driven content generation, review, and refinement, your team can focus on the science— while speeding up the journey to clinical trials.
- Resource Optimization: Collaborate seamlessly with external consultants to deliver top-tier submissions, all while running lean with smaller teams.
- Time-Saving Automation: Generate draft content at the push of a button—because your time is better spent on breakthroughs, not busywork.
- Clarity and Confidence: Move faster without sacrificing accuracy. Trace content back to its source files with ease, ensuring every detail in your content is flawless and precise.
Pharmaceutical
Automate your regulatory documentation process
Pharmaceutical companies face immense pressure to manage complex regulatory submissions, often juggling multiple projects across internal departments and external consultants. Weave’s platform centralizes communication, streamlines collaboration, and leverages AI-driven workflows to supercharge speed, efficiency, and accuracy across every project. With automated, intelligent data management, Weave enables your team to navigate the complexities of regulatory documentation—ensuring you submit with absolute confidence, on time, every time.
- Unmatched Scalability: Handle high-volumes of data with ease, from simple inputs to intricate scientific studies—even when versions evolve.
- Perfect Consistency: When AI is writing it is always the same voice, in your organization’s style, with unvarying structure and level of detail.
- Efficient Global Collaboration: Empower your teams across the globe to work together in real time, eliminating bottlenecks and accelerating your submission timelines.
CROs & Consultants
Optimize your services
For CROs and regulatory consultants, delivering precise, timely, and high-quality submissions is non-negotiable—especially while juggling diverse client demands. Weave transforms your workflow by offering a unified platform to streamline processes, boost collaboration, and guarantee compliance across all projects. With automated solutions that eliminate manual, repetitive tasks and real-time project management tools, you’ll enhance efficiency, expand capacity, and continue to build trust with customers.
- Flexible Client Management: Securely organize client data seamlessly, adapting to the unique requirements of each group, user, and project.
- Uncompromising Precision and Compliance: Harness AI-driven tools to analyze and summarize data, adhere to customer-specific requirements, detect inconsistencies, validate accuracy, and ensure seamless regulatory readiness.
- Scalable Efficiency: Handle multiple projects at once, leveraging your own templates or those required by customers, to efficiently support expanding client portfolios and deliver results faster than ever.