Category: Public Authorities and Safety
With in this category, you may find information about drug safety, regulations, and the role of government agencies in ensuring public health.
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Pharmacovigilance Regulatory Timelines: A Complete Guide
This blog covers: Introduction In today’s regulatory environment, every product must adhere to specific timelines to ensure safety, reliability, and public trust. In the field of drug safety, regulatory timelines play a critical role. They help ensure that safety data is reported and assessed promptly, minimizing risk to public health. Meeting these timelines is not…
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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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📏 IDMP Standardization in PV: Why Are They Essential?
In this extensive blog, you will gain insights into the concept of IDMP standardization. While you might be familiar with the term, its significance might not be fully apparent until you explore its importance in detail here.
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Understanding ICH Guidelines: An Overview
In this in-depth article, we’ll explore various nuances surrounding the International Conference of Harmonisation (ICH) organization, including its facts and guidelines. Let’s delve into the details.
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Understanding the Essence of 21 CFR Part 11
In this extensive blog post, we will explore into the nuances of 21 CFR Part 11, exploring its significance within the pharmaceutical domain and why compliance is essential.
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📜 Role of WHO in Pharmacovigilance
In this blog you will know the details of the World Health Organization’s (WHO) role in pharmacovigilance. If you’re interested in understanding the contributions and significance of the WHO in ensuring global drug safety, you’ve come to the right place.
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🤝 Contribution of CIOMS in Pharmacovigilance: An overview
In this comprehensive blog, we will delve into the fundamentals and history of CIOMS, the Council for International Organizations of Medical Sciences. While many of us are aware that CIOMS is a non-profit organization, its significance goes beyond that.
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📊 Adverse Event Reporting System (AERS) – An overview
Welcome to this insightful blog, where we delve into the purpose and benefits of AERS (Adverse Event Reporting System) and explore how it aids regulatory bodies in effectively addressing the potential harmful effects of drugs on the general population. Join us as we uncover the significance of AERS in ensuring drug safety and public health.
