Regulatory Reimagined
Regulatory documents are critical to your therapeutic candidate's journey, demanding scientific precision, strategic insight, and meticulous planning. With Weave's AI-native regulatory platform, preparing regulatory content is now faster and more efficient than ever.
A living record of your therapeutic candidate.
With the power of AI, regulatory submissions can be generated and constructed, rather than being written. What does that mean? It means you push a button to get a draft. Key details missing? Want a different narrative structure? Need to dial down the level of detail? Simply ask the AI. When you’re ready to review every sentence’s source, it is one click away. Want a table to summarize these studies? Simply ask for it.
From six months, to six clicks with Weave's regulatory automation management platform
Plan and organize files effortlessly
upload
Import source files and summarize instantly
draft
Plan and organize files effortlessly
Draft content in minutes, refine in seconds
REFINE
Optimize content instantly by with AI prompting
Review
Enhance your review team with AI to eliminate tedious tasks
Validate data instantly to reinforce confidence
verify
Confirm accuracy instantly with one click
publish
Publish from a single platform as soon as you’re finished
Try Weave Today
Weave together millions of source threads at the speed of AI and cut your IND application time.
The new standard in regulatory automation and lifecycle management
In today’s fast-paced environment, staying ahead requires speed, precision, and adaptability throughout the regulatory lifecycle. Weave sets a new standard with a software platform that has AI-infused throughout the workflow to simplify complex processes from data organization to submission and beyond.
Our platform provides a single source of truth for the life of your therapeutic candidate, enabling teams to seamlessly collaborate, accelerate project timelines, and deliver high quality, submission-ready content for each required document or report.
Don’t just assemble data, tell the story of your drug.
Accelerate Your Document Drafting
- Auto generate drafts within minutes
- Ensure adherence to regulatory guidelines
- Refine content with AI augmentation
- Maintain complete editing control
- Focus on more meaningful creative and strategic questions
Efficiently Navigate Your Data & Source Files
- Organize content effortlessly
- Tag and search document categories
- Automatically generate summaries
- Trace content to source documents rapidly
- Feel more confident and in control of the process
Streamline Your QC & Review Process
- Auto update quickly with new reports
- Easily resolve IND data conflicts
- Generate reports on affected sections post-update
- Collaborate effectively with multiple reviewers
- Worry less about errors and inconsistencies
