Regulation 37 Interpretation

In this Part—

• “quality records” include inspection reports and test data, calibration data and qualification reports of the personnel concerned;

• “relevant conditions” are that the products conform with the type or modification described in the EC type-examination certificate or additional approval as the case may be and with other relevant requirements of the TTE Directive; and

• “specimen” in relation to a type or a modification means a specimen of the production envisaged in relation thereto.