Document Management / Control for Life Sciences

Dot Compliance Document Management solution is built on the industry best practices ensuring compliance with regulations and standards such as ISO, CFRs & more through GMP/GDocP.

Try Dot Compliance's solution for Document Management free:

	Easily manage the lifecycle of documents & content
	Seamless integration with Office 365
	Most cost-effective & user-friendly DMS
	Adaptable workflows for review and approval
	Part 11 Compliant Electronic signature

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Cloud based, ready to use document management software to manage the entire lifecycle of documents and content - including version control, lifecycle management, annotations, revisions, electronic signatures, and sharing.

Automated eDMS simplifies and ensures compliance with all 21 CFR Part 11 and CFR 820 regulations. Proactively manage regulated content with effective document control and standardized templates for all document types to provide a single source of truth for all internal and external stakeholders.

Ready to use DMS system for life sciences
Access control. Improved compliance. Advanced collaboration.

Facilitate GxP Quality Compliance

Reduce compliance risk with document management SOPs, workflows. Adhere to CFR Part 11 compliant e-signatures to prevent electronic signatures from being modified, duplicated, transferred or removed. Securely manage, track and report on all GxP documents.

Integrated, Connected Processes

Connect all core quality processes with your eDMS solution. The closed loop system seamlessly interconnects your document management system with training management, change control, audits and other core QMS processes.

Ensure Audit Readiness

Ready to use document control solutions make audits simple with detailed audit trails, binder management, and electronic signatures. Easily be prepared for any inspection or audit.

Adhere to industry compliance regulations & standards

For Pharmaceutical
and Biotech Companies

FDA 21 CFR Part 11

EU GMP Annex 11

ISO 9001

21 CFR parts 210 & 211

For Medical Device Companies

ISO 13485

FDA 21 CFR Part 820

ISO 14971

Delivering QMS solutions to QA professionals since 2015

"It is great to be able to use a system that has complete quality management and electronic batch records , as well as forms. The system has an excellent chat function that allows quick communication throughout the company."

Jennifer. H
QA Manager

"The ease of use and linking between modules is great. I use the document module as an electronic validation database and also utilize it to complete validation documentation electronically which is a great benefit to the business."

Neil M.
QA Department Leader

"I really like the Search history section. I also like being able to pin all of the recently searched documents. I also like the communication of DOT Compliance with other software tools we are using in the organization."

Siachalam P.
QA Manager