策划和实施审核以及报告结果和保持记录(见4.2.4)的职责和要求应在形成文件的程序中作出规定。
The responsibilities and requirements for planning and conducting audits, and for reporting results and maintaining records (see 4.2.4) shall be defined in a documented procedure.
生产结束后审核批生产记录，确保生产过程符合工艺规程要求和GMP要求。
Review batch production record after production finished, assure production process conform to process procedure GMP requirements.
根据生产规程以及GMP要求对批次记录以及制程控制报告进行审核。
Review batch record and In-process control report according to process procedure and GMP requirement.
备注：审核员根据现场审核时的实际状况，可能要求抽看其他相关的文件记录。敬请配合支持。
Remarks: Some other documents and records will be required for review as per situation during the onsite assessment. Your cooperation and support will be appreciated.
苹果已经审核了您的购买证明和您的要求来更新我们的记录购买日期。
Apple has reviewed your proof of purchase and your request to update the purchase date in our records.
在产品放行前，质量受权人必须按照上述第2项的要求出具产品放行审核记录，并纳入批记录。
Prior to the release of each batch, the Qualified Person must issue a review record for product release according to the requirements in the above paragraph 2, and archive it to the batch record.
策划和实施审核以及报告结果和保持记录的职责和要求，应在形成文件的程序中作出规定。
The responsibilities and requirements for planning and conducting audits, and for reporting results and maintaining records shall be defined in a documented procedure.
审核小组可能会在现场审核过程中要求查看其它相关的文件和记录。
The audit team may request other related documents and records for review during the onsite audit.
审核小组可能会在现场审核过程中要求查看其它相关的文件和记录。
The audit team may request other related documents and records for review during the onsite audit.
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