Validation Protocol Packaging Including Report EnglishXXX Group CorpMedical Polymer products Co LTDPacking inspect projectName the arts and crafts inspection of packingDocuments serial No VP-002 dr

ion of single packing:4) Peel strength inspection of single packing:5) Seal strength inspection of single packing:6) Appearance inspection of single packing:The second part: the inspection of over-package. Based on the requirements from European Community—Medical Device instruction (MDD93/42/EEC), According to the requirements from EN868-1-Medical Device sterilized packing material and system---the first parts: the general requirements and inspect methods, with regard to our over-package, we carry out the inspections as following:1) Dimension inspection of over-package:2) Visual inspection of over-package:3) Seal inspection of over-package:4) Appearance inspection of over-package:3. Results analysis and appraiseThe inspection results of all the items meet the requirements of EN868-1-Medical Device sterilized packing material and system---the first parts: the general requirements and inspect methods, and also meet the requirements of Medical Device instruction (MDD93/42/EEC).4. Final approvalThe inspection report has been approved and confirmed by all relevant departments.5. Organization of inspectionThe inspection is organized by the Quality Assurance Department.6. Duty and divide the workThe Quality Assurance Department is responsible for drafting the inspection plan, organizing and supervising the inspection, and compiling the inspection report. The Production Department is responsible for providing the samples for inspection, and cooperating with the inspection team during the inspection process. The Engineering Department is responsible for providing technical support during the inspection process. The Sales Department is responsible for communicating with customers about inspection results and handling related issues