Customer testimonials: What life sciences teams say about Sanai
Regulatory, quality, clinical and medical writing leaders at top-20 pharma companies, biotechs, CROs and academic medical centers on how Sanai changed the way they find, draft and control documents.
To protect their privacy, we identify each speaker by role and type of organization rather than by name.
Used by teams at
- Top-20 pharmaceutical companies
- Fortune 500 pharmaceutical companies
- Leading biotech manufacturing organizations
- Medical device companies
- Contract development and manufacturing organizations (CDMOs)
- Contract research organizations (CROs)
- Academic medical centers with clinical research programs
- Multi-site pharmaceutical manufacturing networks
In their words
Validated by regulatory, quality and clinical leaders
In summary · 15 testimonials
Teams describe protocols drafted in minutes and finalized in days, source data found in seconds with its context, CSR writing time cut by 80%, fewer submission delays from automated compliance checks, and version control that tracks every change. The speakers lead quality, regulatory, clinical, medical affairs and medical writing work at top-20 pharma companies, biotechs, CROs, a medical device company and an academic medical center.
What quality and clinical development teams say
As a VP of Quality Assurance, audits are a critical part of my role. Sanai’s AI-powered document management query engine has been a game-changer.
VP of Quality AssuranceMedical device company A clinical trial document such as a protocol is a time-consuming and labor-intensive activity, taking many weeks and multiple team members to contribute. Sanai can draft in minutes and finalize in days.
Clinical Development LeaderTop-20 pharma company Having an easily searchable knowledge base where anyone in the company can find the information they need is a huge time saver for a QA professional. My coworkers can find the forms and processes they need to complete a task right the first time.
Senior Director, Clinical DevelopmentTop-20 pharma company
What teams say about Query Engine
Explore Query EngineFinding the right data used to take hours. Now I get precise results in seconds, with full context about where the information came from.
Senior Regulatory Affairs ManagerGlobal pharmaceutical company The AI understands our GxP language better than most junior staff. It's like having a GxP expert available 24/7.
Clinical Data ManagerCRO specializing in oncology Cross-study comparisons that used to require weeks of manual review now happen instantly with full confidence in the results.
Medical Affairs DirectorBiotech company
What teams say about Document Authoring
Explore Document AuthoringWhat teams say about Document Control
Explore Document ControlSanai Docs eliminated our document chaos. We now have complete visibility into our regulatory document landscape with full compliance confidence.
Director of Quality AssuranceMid-size pharmaceutical company Version control used to be our biggest headache. Now we track every change automatically with complete impact analysis.
Regulatory Operations ManagerGlobal biotechnology company The automated compliance checking has prevented multiple submission delays. It's like having a regulatory expert reviewing every document.
VP of Regulatory AffairsClinical research organization
What medical writers say
Sanai for Medical WritingFinally, a tool that understands medical writing isn't just about grammar—it's about compliance, accuracy, and clear communication.
Senior Medical WriterTop-10 CRO We've stretched our grant budget 40% further by reducing the time spent on document formatting and revisions.
Grant-funded research teamAcademic medical center The institutional review process used to be our bottleneck. Now we submit cleaner documents that sail through approval.
Medical Writing ManagerPhase III oncology program