Regulatory aspects of ayurvedic medicines around the globe: An Updated review
European Journal of Molecular & Clinical Medicine,
2022, Volume 9, Issue 7, Pages 9093-9115
Abstract
Pharmaceuticaldrugregulatoryaffairscoversdifferentregistrationparameterofpharmaceuticalproduct. Asitisthenewprofessionwhichwasdevelopedfromthedesiredof all over the world to protect the public health by providing good quality of medicineincluding safety and efficacy in the area of not only pharmacy but also in the area of theveterinary medicine, medical device, insecticides, pesticides, agrochemical, cosmetic andcomplementary medicine. It also made the interface between the pharmaceutical companyand the regulatory agencies. It is also responsible for maintaining the appropriateness andaccuracy of the product information. And its main role to act as an liaison with regulatoryagencies,providingexpertiseandregulatoryintelligenceintranslatingregulatoryrequirement into practical workable plan, advising the company on regulatory aspects andclimatethatwouldaffecttheirproposedactivities
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