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About Dock by ProtoEng

A CFR compliant Document Management system for holding auditable records with signatures (Such as for Medical Device manufacturing).

Our Mission

Dock by ProtoEng is built to streamline document creation, review, and approval processes while maintaining strict adherence to regulatory standards. Our system ensures your auditable records are always secure, traceable, and compliant.

We provide a centralized platform for managing documents, e-signatures, and quality records, reducing overhead and mitigating compliance risks for medical device manufacturers and other regulated industries.

What We Offer

Document Control

Robust versioning, draft management, and structured approval workflows (such as ECNs and ECRs) tailored to your organization's needs.

Electronic Signatures

Secure, legally binding 21 CFR Part 11 compliant e-signatures integrated directly into your review and approval processes.

Built for Compliance

Audit Trails

Comprehensive and immutable audit trails tracking every action, from draft creation to final approval and archival.

Secure Access Control

Role-based access controls and multi-factor authentication to ensure only authorized personnel can access or modify your critical records.

Regulatory Reporting

Generate necessary compliance reports easily and ensure readiness for internal and external quality system audits.

Get In Touch

Interested in learning more about Dock by ProtoEng or have questions about how we can help your organization maintain compliance? We'd love to hear from you.