Regulatory Requirements and Guidelines
ICH E2E Guidelines The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) provides the E2E […]
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Basics of Aggregate Reporting
Aggregate reporting in pharmacovigilance refers to the process of compiling and analyzing data on adverse events from various sources to
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MedDRA in Different Languages
In the world of medicine, communication is key. And when it comes to international communication, language can often be a
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Advantages of MedDRA
MedDRA, with its comprehensive and hierarchical structure, brings a plethora of advantages to the table. It’s like a Swiss Army
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Usage of MedDRA
The usage of MedDRA is as diverse as the medical world itself. It’s like a Swiss Army knife, serving multiple
Organization of MedDRA
The organization of MedDRA is one of its most unique features. It’s structured in a hierarchical manner, which means it’s
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History of MedDRA
The journey of MedDRA, like any great invention, started with a need. A need for a common language in the
Introduction to MedDRA
MedDRA, short for the Medical Dictionary for Regulatory Activities, is a clinically validated international medical terminology. It’s like the universal
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Role of Literature Reports in Drug Safety
Literature reports in pharmacovigilance are like the unsung heroes of drug safety. But what role do they play? Let’s delve
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