Section 4. LABORATORIES OF QUALITY CONTROL OF DRUGS AND OTHER PHARMACEUTICAL PRODUCTS Article: 39 Laboratory of quality control means any establishment dealing with quality analysis drugs and other pharmaceutical products, and with control of their conformity to the official standards. The results of analysis shall be recorded in a register reserved to that end. The register be kept for at least ten years from the closing date. Article: 40 Laboratory of quality control means any establishment dealing with quality analysis drugs and other pharmaceutical products, and with control of their conformity to the official standards. The results of analysis shall be recorded in a register reserved to that end. The register be kept for at least ten years from the closing date. Article 40: Authorization issued by the Minister responsible for Health shall specify the dully authorized types of analysis. Any rectification of types of analysis shall be subject to prior authorization issued by the Minister responsible for Health. Title III. DRUGS AND OTHER PHARMACEUTICAL PRODUCTS Chapter 1. GENERIC DRUGS AND PHARMACEUTICAL SPECIALITIES Section 1. RECORDING OF GENERIC DRUGS AND PHARMACEUTICAL SPECIALITIES Article: 41 Generic drugs means any drug, non protected by a patent, industrially prepared, a marketed unded the common international denomination of the active principle followed or not by the manufacturer's name.