本公司依照國際法規ISO 17025和 GLP 規範精神，測試均遵守“良好實驗室實踐非臨床實驗研究”，以及質量保證單位分別審核設施、設備、人員、試驗方法、原始數據和原始記錄等。 研究報告進行了審查，並提出內部批准。所涉及的實驗，所有部分均按照製造商方法進行。所有的原始記錄，原始數據和文件如實轉移於結果報告中。遵守任何記錄都歸檔在研究記錄。沒有偏差影響研究數據的有效性。
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.