Frequently Asked Questions

dosyap is an AI-powered Regulatory Affairs automation platform that helps pharmaceutical companies prepare, localize, and validate CTD and eCTD files faster and with higher accuracy.
Before processing, the platform automatically performs OCR (optical character recognition) and file size reduction to ensure all documents are readable, optimized, and compliant before upload.

dosyap helps Regulatory Affairs teams overcome:

• Delays in dossier preparation and localization,

• Manual inconsistencies between reference and local files,

• Limited visibility across multi-country submissions, and

• High resource dependency for repetitive formatting and QC steps.

Through AI automation and workflow tracking, Dosyap ensures faster, transparent, and controlled regulatory operations.

Our automation engine analyzes reference EU files, performs gap analysis, and generates local submissions up to 4× faster than traditional manual workflows — while ensuring regulatory consistency and data integrity.

dosyap supports both Word (.docx) and PDF formats for uploading and processing regulatory documents. More formats will be added as part of our continuous platform updates.

Before accessing the platform, all clients sign an NDA (Non-Disclosure Agreement).
Your uploaded files are processed in a secure, GxP-compliant environment and never shared externally.

Yes. You can book a demo through the “Get a Demo” button or contact our team to schedule a personalized walkthrough of the platform.

To begin, contact us through the Consultation Form on our website.
Once we receive your request, our team will share an NDA (Non-Disclosure Agreement) for signature and set up your secure workspace for onboarding.