SOC 2Type II Certified
SOC 3Certified
GDPRCompliantKeep legal running at the speed of your product pipeline.
Supplier agreements, distribution deals, co-development terms. GC AI reviews them against your standards so your team can focus on R&D strategy and regulatory risk.
What to expect:
- A detailed walkthrough of GC AI tailored to your medical device and research agreement review, regulatory compliance, IP management, and supplier relationship use cases.
- Answers on security, integrations, and onboarding for your team.
- A 14-day free trial.
Trusted by legal teams at world-class companies
“The policy development process has sped things up so much... what would have taken forever to do manually is now much faster.”
Misty Premo“Thank you, GC AI, for saving my sanity this morning. You helped me quickly draft an amendment to a contract that would have taken me an hour to do by hand. It saved my sanity because I can now get to the beach to take a surf lesson with my son”
VP Legal“GC AI aka CARL is my new best friend. If it was a human, I would hug it and tell it every day how happy I am to have it in my life. Thank you for everything you are doing behind the scenes to keep making it better.”
“I am a big skeptic of legal AI tools having evaluated many (Harvey, Jurist, Spellbook AI, etc.), but GC AI is definitely the market leader and a great tool that I use daily now. The UX/UI is very clean, the legal analysis it provides is very good when paired with the expectations I have for it, and the training your team provides is very helpful. Happy to be a customer and looking forward to using GC AI further.”
Everything your legal team needs, in one place.
From better prompts and real citations to reusable skills and in-Word editing. Everything just works together, so your team can focus on the legal work that matters.
Primary use cases for medical devices and research legal teams
Supplier terms, co-development deals, IP licenses, clinical agreements. GC AI checks them against your standards and surfaces the regulatory and IP issues worth your time.
- Supplier Agreements
- Review supplier and component sourcing agreements for commercial terms, obligations, and supply chain risks.
- Clinical Agreements
- Analyze clinical evaluation and study agreements to identify responsibilities, timelines, and compliance requirements.
- Distribution Agreements
- Review distribution and commercialization agreements for key terms, obligations, and market rights.
- Quality Compliance
- Review quality and regulatory compliance agreements to ensure obligations align with industry requirements.
- R&D Collaboration
- Analyze co-development and research collaboration agreements for ownership, responsibilities, and project terms.
- Regulatory Documents
- Review FDA and CE mark-related documentation for accuracy, completeness, and regulatory compliance.
- IP Assignment
- Review IP licensing and patent assignment agreements to clarify ownership, rights, and licensing terms.
- Consulting Agreements
- Review independent contractor and consultant agreements for responsibilities, liabilities, and engagement terms.
Common questions
Is GC AI built for medical device and research legal teams?
Yes. GC AI is built for in-house legal teams at medical device companies, CROs, and research organizations. The platform handles high-volume work across supplier agreement review, IP licensing, regulatory documentation, and co-development arrangements, so your team can focus on R&D strategy and regulatory risk. GC AI's Research deploys multiple agents across authoritative legal and regulatory sources, so your team can track FDA guidance and patent obligations with cited answers.
Can GC AI review our vendor, supplier, and MSA agreements?
Yes. GC AI reviews commercial agreements end-to-end, flagging issues, drafting missing clauses, and summarizing terms in seconds. Build GC AI Playbooks from your standards so every agreement is reviewed the same way.
How does GC AI keep our data secure?
GC AI is SOC 2 Type II and SOC 3 certified, GDPR compliant, with zero data retention agreements with OpenAI and Anthropic, and AES-256 encryption. We provide documentation on request for procurement. Read our Security and Privacy FAQs and visit the GC AI Trust Center as well.
How long until our team sees value?
80% of GC AI users see value within the first day, and 97.5% before month one. Read more about our study, Legal AI's Time-to-Value for In-House Counsel.
What is the difference between GC AI and Harvey?
GC AI is built exclusively for in-house legal teams, with workflows, output style, and pricing designed for corporate counsel. Harvey initially launched with law firms and has since expanded to in-house. GC AI's founder is a three-time General Counsel; Harvey's co-founder comes from Big Law. GC AI's outputs are concise and business-focused, shaped by a 20,000-line system prompt. See the comparison.
Can GC AI help manage IP and patent-related agreement language?
Yes. GC AI reviews IP assignment clauses, licensing agreements, and joint development arrangements, so your team can protect core patents and innovations as you bring new devices to market. The Skill Library includes pre-built workflows for IP assignment and license agreement review, so your team can run consistent reviews from day one.
Can GC AI help with supplier and distribution agreement review?
Yes. GC AI reviews supplier agreements, distribution arrangements, and co-development deals, flags non-standard quality, liability, and regulatory compliance provisions critical in the medical device supply chain, and catches issues before they affect product timelines. Use the GC AI for Word Add-in to redline supplier terms directly inside your document.
SOC 2Type II CertifiedSOC 3CertifiedGDPRCompliantKeep legal running at the speed of your product pipeline.
Supplier agreements, distribution deals, co-development terms. GC AI reviews them against your standards so your team can focus on R&D strategy and regulatory risk.
What to expect:
- A detailed walkthrough of GC AI tailored to your medical device and research agreement review, regulatory compliance, IP management, and supplier relationship use cases.
- Answers on security, integrations, and onboarding for your team.
- A 14-day free trial.