The landscape of compliance is changing. Artificial intelligence is rapidly streamlining the traditional systems for document control and creation. We are dedicated to ensuring that experts in these fields have a seat at the table and maintain the final human touch.
Shape the emerging role of artificial intelligence in regulatory compliance.
SE.ai is looking for specialists including consultants, technical writers and other FDA domain experts interested in redefining the regulatory industry.
Join our Expert Program today to:
Increase your business
Gain access to hundreds of medtech projects ready for input from regulatory experts like you.
Increase your productivity
Utilize our platform to assist in rapid documentation drafting from scratch for your firm’s projects.
Pioneer a new industry
Define, optimize and maintain the role of regulatory experts in the age of artificial intelligence.
3 steps to grow your business and organize your workspace.
Step 1: apply for our EXPERT PARTNERSHIP program
Sign up for our Expert Program today to access our revolutionary tools for navigating FDA approval.
step 2: Sign up for a Package that works for your team
Define a package that delivers results for you, and help our R&D team prioritize features you need.
step 3: Increase your Throughput and bottom line
Utilize our custom AI toolbox to draft documents in 5X less time. Take more clients and grow your business.
Frequently asked questions.
How much does the program cost?
Our Expert Program is currently 100% free to for all qualified applicants for our reviewer modules. Experts who wish to utilize our builder toolbox are still eligible for discounts at this time.
What can I expect out of the program?
You can expect to gain access to our AI toolbox for drafting and editing documents for FDA 510(k) projects.
How do I request more information?
If you are interested in learning more about our program before applying, contact our team to schedule an introductory meeting or phone call.
SE.ai 