不知道我们的GMP为什么一定要“实样”,这个在实际的操作中也不可行,比如预印的瓶子和罐子,那么是否必须要将瓶子和罐子也附入到批记录中????
其实在USA CGMP中有提到:
§211.186 Master production and control records.(b) Master production and control records shall include: (8) A description of the drug product containers, closures, and packaging materials, including a specimen or copy of each label and all other labeling signed and dated by the person or persons responsible for approval of such labeling; §211.188 Batch production and control records.(b) Documentation that each significant step in the manufacture, processing, packing, or holding of the batch was accomplished, including: (8) Complete labeling control records, including specimens or copies of all labeling used; 457. Several comments regarding 211.186(b)(8) and 211.188(b)(8) said lithographed bottles, cans, and ampules cannot be kept on file. The Commissioner notes that the final regulations provide that a "specimen or copy" be included in the master and batch production or control record. A photograph, photocopy, or other accurate reproduction will fulfill the intent of these sections.那么说明使用相应的accurate reproduction也是合适的,同时我们的法规针对于说有的“所用印刷包装材料”也很不实际,如果仅仅是外箱,印有简单的公司描述性文件,那么是否也需要包括进入???无法操作,而USA cGMP则仅仅限于labeling |