Good Manufacturing Practice (GMP) is the name of the set of requirements that must be met by drug manufacturers when manufacturing pharmaceuticals. These standards ensure that the product produced and controlled is of high quality and safe. Current Good Manufacturing Practice (cGMP) is the name of the development of the mentioned standards. It ensures that manufacturers have to be in compliance with the latest regulatory requirements and procedures, keeping production documents intact. With the cGMP requirement, pharmaceutical firms need to observe stringent quality control measures in order to ensure that their products are both safe and effective for consumers. These measures include testing at all production levels, proper documentation, and procedures, among others. By following these requirements, pharmaceutical companies will be able to show that their drugs comply with the highest standards regarding safety, efficacy, and quality assurance.  cGMP also promotes innovation in the processes of pharmaceutical production as well as improvement of the existing methods. By keeping themselves informed about the latest standards and guidelines, pharmaceutical companies will be able to produce their drugs safely, effectively, and at a high level of quality.  To sum it up, GMP is a set of minimal requirements that pharmaceutical producers must follow in order to guarantee the safety and quality of their products. In contrast, cGMP includes more measures to keep the pharmaceutical industry compliant with the newest regulations. By complying with all the requirements, pharmaceutical producers will be able to offer consumers only safe and effective pharmaceuticals.