COMPLIANCE CAN BE EASY TO ACHIEVE
FDA UDI, EU MDR, FDA PART 11, EU Clinical trials
regulations can be easily implemented with the right
Let us help you
IS YOUR ROLE REGULATORY OR COMPLIANCE?
Ensuring that your company is fully compliant with all required medical device or clinicla trials laws and regulations, is not only fundamental but also incredibly time-consuming. However, as important, is ensuring you remain fully up-to-speed on all aspects of legal change.
Our internal regulatory experts quote: “If you cannot prove it, it did not happen.”
We understand that you need to be supported by highly efficient Label Management Software and documentation for all aspects of compliance - from FDA 21 CFR Part 11, Audit logs, Approval Workflows, Language and Phrase Controls, Print Inspection, and Versions Control to Regulatory Rules and Security.
We support every element of validation - from initial installation to final performance testing, if support is required. Our software is supplied as a validatable package, including auditable security protocols and lifecycle documentation, based on the GAMP 5 model.
“Security and regulatory compliance is of paramount importance in medical device manufacturing. PRISYM ID’s labeling system is able to provide us with the correct level of service and security we require, whilst being user friendly.
The install of the system into our clean room went smoothly and we have been pleased with the results.”
CHOSEN BY THESE CUSTOMERS...
OFFERING THE PERFECT OPTION FOR YOU
Label and Artwork Management Solution for Medical Device, Clinical Trials and Pharmaceutical sectors.
We offer tiers of deployment to suit your needs and size of the business. But our offer is much more than just deployment.
We are the only software vendor in life science industry who supplies in- house validation documentation and implementation support.
REGULATORY AND COMPLIANCE LABELING RESOURCES
Discover how PRISYM ID helped Origen Biomedical, a growing medical device manufacturer, who was looking for a cost effective and easy to use label printing process.
Changing regulations, such as Annex VI clinical trial regulation, need to be incorporated into the label and artwork processes in time for when the regulation takes effect.