´本公司依照國際法規ISO 17025和 GLP 規範精神
´For the study is to comply the “Good Laboratory Practice for Nonclinical Laboratory Study”, and the Quality Assurance Unit audited the facility, equipment, personnel, test methods, raw data, and original records, respectively.
´The study report has been reviewed and presented internally approved. All parts of the experiments involved were conducted according to the manufacturer's protocol. All original records, raw data, and documents are truthfully transferred and addressed in the results of this report. Any areas of non-compliance are documented in the study records. No deviation impacted the validity of study data.