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.