Regulatory has one home.
It's where our AI-native software meets your human expertise.
Regulatory documents aren’t just paperwork—they’re a vital component of a drug’s development journey. They narrate the story of a therapeutic candidate’s rise or fall in the competitive landscape of pharmaceuticals. Behind every page is a dedicated team of experts navigating tight deadlines, scientific complexities, and relentless organizational pressures.
Weave’s regulatory automation management platform empowers you to take control of this process. It equips every stakeholder involved in document preparation with the tools needed to work at lightning speed, make informed decisions, and proactively address submission risks before they arise.
Biotech
Accelerate your time to market and milestones
In the competitive world of startups and small biotechs, operational efficiency isn’t just a luxury—it’s a survival strategy. Weave empowers your team to streamline regulatory workflows, allowing you to do more with less by automating the regulatory processes that typically 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 accelerating the journey to clinical trials and enhancing regulatory compliance.
- Intelligent Document Management: Organize and access all regulatory documents effortlessly, reducing time spent on administrative tasks.
- Time-Saving Automation: Generate initial drafts at the push of a button, significantly reducing preparation time and enabling your team to focus on advancing critical therapies.
- Automated Quality Assurance: Utilize advanced validation tools to verify content accuracy and ensure alignment with regulatory standards, giving you confidence in your submissions.
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 and streamlines collaboration, leveraging AI-driven workflows to enhance speed, efficiency, and accuracy across every regulatory project. With automated, intelligent data management, Weave empowers your team to navigate the complexities of regulatory documentation—ensuring you submit with 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 regulatory submissions is non-negotiable—especially while managing diverse client demands. Weave transforms your workflow by providing a unified platform that streamlines processes, enhances collaboration, and ensures compliance across all projects. With automated solutions that eliminate manual, repetitive tasks and real-time project management tools, you’ll improve efficiency, increase capacity, and continue to build trust with your clients.
- 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.