TouchMark is ISO 9001 Certified and FDA QSR Compliant
TouchMark is committed to meet or exceed customer quality standards and maintains a documented Quality Assurance System that ensures adherence to the processes and procedures outlined in ISO 9001:2008 Standards.
TouchMark works closely with Medical Device Manufacturers to establish and follow quality systems to help ensure that their products consistently meet applicable FDA requirements and specifications.
As part of its Quality Assurance Program, TouchMark Delivers:
- Product Traceability to Batch Level
- Incoming Material Inspection
- Maintained Lot Integrity
- Ink Adhesion Tests – Standard and Customer Specified
- Optimum Ink Selection and Surface Preparation
- Final Inspection Reports
Cleanroom Manufacturing Environment
TouchMark manufactures in a controlled cleanroom environment on state-of-the-art equipment to ensure process control, repeatability, production efficiency and reliability.