What Is IVDR (2017/746) Consulting?
Consulting on risk classification, technical documentation, performance evaluation and post-market surveillance for IVDR (2017/746) compliance.
READ MORE: What Is IVDR (2017/746) Consulting?News
We Successfully Completed the Audit at Disposed Healthcare Products
We successfully completed the audit process conducted by HTCERT at Disposed Healthcare Products.
READ MORE: We Successfully Completed the Audit at Disposed Healthcare Products
IVDR Transition Process
IVDR transitional provisions, the date of application and the proposed transition timelines for certain in vitro diagnostic medical devices.
READ MORE: IVDR Transition Process
Validity of ISO 13485 QMS Certificates After Brexit
The validity of ISO 13485 quality management system certificates under UKAS and RvA accreditation after Brexit.
READ MORE: Validity of ISO 13485 QMS Certificates After Brexit
What Is MDR Certification?
The MDR certification process, the safety, performance and quality requirements medical devices must meet, and the benefits it offers manufacturers.
READ MORE: What Is MDR Certification?ARE YOU LOOKING FOR AN
Experienced Consultant?
Contact us right now