CERTIFICATE OF ANALYSIS (COA) GENERATION PROCESS Created by ChecklistGuro (https://checklistguro.com) [ ] Fetch Batch Production Data: Retrieve all raw material test results and production parameters from the Batch Data Model. [ ] Fetch Product Specifications: Retrieve the predefined acceptance criteria (min/max limits) for the specific product SKU. [ ] Calculate Average Purity: Calculate the average purity percentage from all sampled test entries in the batch. [ ] Check Specification Compliance: Compare the aggregated test results against the product specification limits to determine pass/fail status. [ ] Update Batch Quality Status: Update the 'Quality Status' field in the Batch Data Model to 'Review Pending' or 'Passed/Failed'. [ ] Quality Control Review Task: Create a task for the QC Manager to review the calculated results and verify laboratory findings. [ ] Create CoA Draft: Generate a new entry in the Certificate of Analysis Data Model populated with the processed data. [ ] Populate CoA Details: Write the specific test values, dates, and technician names into the newly created CoA entry. [ ] Final Approval Task: Create a task for the Quality Assurance Lead to digitally sign and approve the CoA. [ ] Generate PDF Certificate: Generate the formal, printable PDF document representing the Certificate of Analysis based on the CoA entry data. [ ] Finalize CoA Status: Update the CoA entry status to 'Released' or 'Archived'. [ ] Notify Production Team: Send an email to the Production Manager with the link to the completed CoA. [ ] Notify Client (If Failed): Send an automated email to the client contact if the specification compliance calculation resulted in a 'Fail'. --- END OF TEMPLATE --- Transform this text into a digital, automated, and trackable mobile app! Visit: https://checklistguro.com/workflow-templates/pharmaceutical/certificate-of-analysis-coa-generation-process (Click "Install Template" to launch your digital inspection tool immediately)