302车间引入来那度胺胶囊5mg&10mg&25mg的变更（后续处理）

302 workshop introducing changes capsules lenalidomide (subsequent process) 5mg & 10mg & 25mg of: <br>1. Cancel lenalidomide product into capsules 4 F workshop production line 302, terminating registration application. <br>2.302 workshop to original documents lenalidomide capsules products related to the cancellation, copy recovered and destroyed. Reserved lenalidomide quality standards, and update files. <br>3. Destruction R & D stock lenalidomide capsules products. <br>4. Update "formulation qualified suppliers directory" cancel special raw materials lenalidomide capsules involved. <br>5. Cancel lenalidomide intermediate capsule products, special raw materials and finished products SAP material code system. "

302 workshop introduced to nala amine capsule 5mg s 10mg s 25mg changes (follow-up treatment):<br>1. Cancel the introduction of the Nadu amine capsule products into the 302 workshop 4th floor production line, terminate the registration declaration.<br>2. The original documents related to the 302 workshop to nala amine capsule products are cancelled, copies are recovered and destroyed. Keep that degree amine quality standard and update the file.<br>3. Destroy the finished product of the Nadoamine capsule in the research and development inventory.<br>4. Update the "Preparation Qualified Supplier Catalog" and cancel the special raw materials involved in the Nadu amine capsule.<br>5. Cancel the intermediate, finished product and special raw material material code of the naamine capsule product in the SAP system. "

Change of lenalidomide capsules 5mg-10mg-25mg introduced into workshop 302 (follow-up treatment):<br>1. Cancel the introduction of lenalidomine capsule products into the production line on the 4th floor of workshop 302, and terminate the registration application.<br>2. The original documents related to the products of lainaduandiamine capsule in workshop 302 are cancelled, and the copies are recovered and destroyed. Retain the quality standard of lenalidomine and update the document.<br>3. Destroy the finished lenalidomine capsules in the R & D inventory.<br>4. Update the list of qualified preparation suppliers, and cancel the special raw and auxiliary materials involved in lenalidomide capsule.<br>5. Cancel the codes of intermediates, finished products and special raw and auxiliary materials of lenalidomine capsules in SAP system. "