The simple and effective way of managing quality processes and safeguarding compliance
Electronic quality management systems should be usable, reflect current regulatory processes and be on a stable technology. X-docs has been built and maintained to those requirements. X-docs delivers efficiency that can be measured in working time saved and the intangible benefits of allowing the Quality Professional to focus on business improvements rather than administrative tasks.
Ready to Go
Out of the Box EQMS functionality including SOP documents, CAPA processes and Training records with quick and easy implementation.
Pre-Configured software designed for use in Life Science so validation is minimal and supported by Formpipe templates.
Allowing your system not only be a compliance tool but also drive Quality led business decisions. Reporting is adapted to meet your needs.
Let X-docs help you help yourself
If you take a look at our brief product presentation video, we will literally change your life (at least the part where you’re fed up with quality systems that don't meet Life Science needs, the rest is still up to you).
Some key features
Ready to go: Pre-configured workflows and structures.
Easy to configure: Sharepoint tools for simple administration.
Fully compliant: Meets FDA, EU & MHRA regulation.
Powerful reporting: Supports data-driven decisions based on Quality metrics.
Return on investment: Delivers efficiency that outweighs the system investment.
Pre-configured, Life Science compliant and efficient EQMS available out of the box
Designed, maintained and implemented by Life Scientists – X-docs is an easy to use EQMS solution that reflects current regulatory procedures for the FDA, MHRA and EU markets. Delivered on a stable Sharepoint platform it offers pre-built modules and workflows that can be adopted Out of the Box or configured to meet individual needs the result being the easiest and quickest EQMS to deploy within a regulated environment.
The solution is scalable for up to 500 daily users and has a full and filterable audit trail, cross modular functionality and a proven migration path. X-docs also has FDA CFR 21 Part 11 compliant electronic signature.