Tag: PV regulations
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Quality Management System
In this blog, you will discover essential insights for enhancing your company’s quality, guided by the principles of GVP (Good Pharmacovigilance Practice). It contains a concise summary of critical information derived from GVP that is imperative for your knowledge.
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Regulatory Submissions in PV: Key Set of Rules
This blog covers the following topics: Introduction Today, almost every product we use is subject to regulatory oversight, not limited to medicines. Regulatory duties involve monitoring, market availability and ensuring its safety. When it comes to pharmaceutical products, the regulations are even more stringent due to their direct impact on public health. Each drug governed…
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Exploring Pharmacovigilance in Georgia
This blog covers the following topics: Introduction Many people are familiar with the name Georgia, often associating it with the U.S. state. But, in this article, we are exploring about the country of Georgia. A beautiful nation nestled between the Caucasus Mountains, bordered by Turkey, Armenia, and Azerbaijan. This time we explore the pharmacovigilance activities…
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🇬🇧 Post-Brexit Pharmacovigilance in the UK
In this comprehensive blog, we delve into crucial aspects concerning the impact of Brexit on pharmacovigilance activities. We outline key points that deserve attention.
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The Clock is Ticking: Significance of Regulatory Timelines
From this blog, where you systematically explore regulatory timelines based on case criteria determined by authorities. If you’re looking to navigate the complexities of regulatory timelines, you’ve come to the right place.
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Role of Drug Regulatory Bodies: Guardians of Public Health
In this comprehensive blog, where we delve into the world of regulatory authorities and their dedicated roles. If you’ve ever wondered about the crucial functions performed by regulatory bodies, you’ve come to the right place.
