STANDARDS
The LPE Medical team can contribute and support your projects from concept through to design and manufacture. With concurrent engineering and bespoke quality planning we can fully integrate our sub-contract processes into your supply chain. Our unique flexibility ensures that whether you choose to take advantage of our ability to supply finished packaged product or utilise any of our individual areas of expertise, LPE Medical will complement and strengthen your existing design, manufacturing and production resources
Quality Assurance and Good Manufacturing Practice are integral to LPE Medical operations. Our quality system is certified to the relevant ISO series standards and is subject to regular internal and external audit.
Material process traceability is guaranteed and all our process inspection data is retained and stored as required by international standards. Our quality reporting dossiers and manufacturing batch records can be tailored to meet your specific requirements.
WE CAN INCLUDE ANY OF THE FOLLOWING
- Risk Analysis
- Statistical Process Control
- Process Validation Protocols &
Reports
- First Article Inspection
- Process Capability Studies
- Gauge R & R
- Quality Plans

