This bilingual CN-EN checklist helps equipment and production teams in medical device manufacturing audit critical areas: buffer and transfer rooms, pellet room, injection molding, printing and silicification, assembly, packaging, and needle assembly. It emphasizes validation and maintenance records, correct SOP usage, process parameter controls, equipment status identification, and proper documentation. The checklist also verifies PPE compliance, housekeeping, and organization at the point of use. Auxiliary systems such as HVAC, air blowers, ozone treatment, and purified water are included, with requirements for usage logs, acceptance records, annual maintenance plans, and verification reports.
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This community page makes available free workplace checklists and templates created by other users within the SafetyCulture community. SafetyCulture has re-published this content and where possible, has credited the original author. SafetyCulture has not verified the accuracy, reliability or suitability of any community content. You agree that your use of any of this content is in accordance with SafetyCulture’s Terms and Conditions.