Tag: Drug safety

Good Pharmacovigilance Practices by EU

Understanding Good Pharmacovigilance Practices (GVP): Ensuring the Safe Use of Medications

At Vigilare Biopharma We strongly believe that medications play a crucial role in modern healthcare, but their benefits are intricately linked to their safety. A robust pharmacovigilance system is vital to ensure that medications are

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Regulatory News

Pharma and Regulatory News Sep 22

New ZLG Document on Transport Verification Published At the end of August, the German Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (Zentralstelle der Länder für Gesundheitsschutz

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Outsourcing Pharmacovigilance to CROs: Benefits, Challenges and Best Practices

How CROs Can Support Pharmacovigilance and Regulatory Compliance? Pharmacovigilance is the process of monitoring, evaluating, and preventing adverse reactions or any other problems related to medicines. It is an essential part of drug development and

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How decentralized clinical trials-DCTs are transforming clinical research and patient care?

DCTs are not a fad, but a trend that is transforming clinical research and patient care. By leveraging technology to make trials more accessible

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Patient Engagement in Pharmacovigilance: Empowering Patients for Safer Healthcare

involving patients directly in pharmacovigilance efforts can be a game-changer. Patient engagement offers unique insights, enhances reporting systems, and fosters a collaborative approach to drug safety.

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Pharmacovigilance in Medical Trends: Enhancing Drug Safety in the Evolving Healthcare Landscape

As healthcare advances, new treatment modalities, personalized medicines, and innovative technologies are reshaping the landscape.

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Regulatory News

Regulatory and Pharma News July 21

Welcome to the latest edition of our Pharma News and Regulatory News Updates, where we bring you the most significant developments and breakthroughs in the pharmaceutical industry and the latest updates from regulatory agencies worldwide.

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Pharmacovigilance Guidelines: Ensuring Global Drug Safety

Pharmacovigilance guidelines serve as essential frameworks and standards that govern the practice of pharmacovigilance globally. These guidelines provide guidance and recommendations for various stakeholders involved in drug safety monitoring, including regulatory authorities, pharmaceutical companies, healthcare

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Clinical trials and their phases

Clinical trials and their phases?

Clinical trials happen in several phases during which different questions are asked. Each phase builds on the results of previous phases

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Adverse Drug Reactions Reported Each Year On Rise

ADRs refer to harmful or unintended reactions caused by the use of medications or medical treatments. They range from mild side effects to severe and life-threatening events

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