The AI based Smart Pharma Lab Solution.
ELN Templates
Jumpstart your documentation with submission-ready templates.
ICH Q2(R1) Validation Report
Validation
Template for analytical procedure validation as per ICH guidelines.
FDA 21 CFR Part 11 Compliance
Compliance
Checklist and report template for electronic records and signatures.
Method Development Report
Development
Standardized format for documenting the development of new analytical methods.
Stability Study Protocol
Stability
A comprehensive protocol for initiating and managing stability studies.
Annual Product Review (APR)
Quality Assurance
Template for conducting and documenting Annual Product Reviews.
