AbstractThe mission of achieving good manufacturing practice (GMP) license for the drugs production is to ensure the quality and efficacy of pharmaceutical products, thus assure the public safety. Compliance of GMP standard can increase the competitiveness, efficiency of production, images for pharmaceutical manufacturing firms against international market development. In meeting these ends, pharmaceutical firms must assure that the manufacturing processes, verifications of the end products, validations of the manufacturing processes and equipment as well as the inspection equipment and procedures are properly conducted with a proper documentation system. The authors will focus on the strategic implementation of GMP.