Managing pharmacovigilance for biosimilars necessitates a deep understanding of the reference product and the evolving regulatory landscape. In the latest article by Ivana Lisec for Pharma's Almanac, discover how PrimeVigilance supports biosimilar developers with practical, expert-driven solutions. Read the article: https://lnkd.in/eXnQT_S2 #Biosimilars #Pharmacovigilance #PrimeVigilance #PatientSafety
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💡 What are the current and future changes in the pharmacovigilance field and how does technology play a critical role? 📑 Our whitepaper will help answer these questions and provide insights into the dynamic evolution of pharmacovigilance ➡️ https://zurl.co/FdL2 In the last fifteen years, Pharmacovigilance has evolved from a simple function within regulatory compliance to an integral and proactive activity in the safety of drugs and devices for clinical use and post-marketing. Discover more now! #pharmacovigilance #PV #technology #safetydrugs #lifesciences #pharma
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"Excited to share that I've earned a certificate in Pharmacovigilance!" This course has deepened my understanding of drug safety and monitoring, equipping me with the knowledge to contribute effectively to the pharmaceutical industry. Looking forward to leveraging these skills to ensure patient safety and enhance healthcare outcomes. #Pharmacovigilance #DrugSafety #HealthCare #ProfessionalDevelopment #CourseCompletion
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🎉 Excited to share that I’ve successfully completed a course in Arab Clinical Research and Pharmacovigilance Guidelines! 📚✨ This journey has enriched my understanding of region-specific healthcare protocols, ensuring patient safety through efficient drug monitoring and regulatory compliance. Looking forward to applying this knowledge in the clinical research landscape and contributing to impactful healthcare innovations. #ClinicalResearch #Pharmacovigilance #ArabGuidelines #HealthcareCompliance #PatientSafety #ClinicalTrials #Pharma #ResearchInnovation #Emirateshealthauthority #Pharmaceuticals #UAE
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📌 An Overview of Clinical Research 👉 Follow PV Drug Safety Academy for more insights. #clinicalresearch #clinicaltrials #pharmacovigilance #drugsafety #patientsafety
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Clinical research and pharmacovigilance are inextricably linked in the life cycle of a medicine. While clinical research enables treatments to be discovered and evaluated, pharmacovigilance ensures that they are used safely. Together, they form a robust system that protects patients' health and fosters medical innovation.
📌 An Overview of Clinical Research 👉 Follow PV Drug Safety Academy for more insights. #clinicalresearch #clinicaltrials #pharmacovigilance #drugsafety #patientsafety
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🛡️The Crucial Role of Pharmacovigilance in Pharma🛡️ Pharmacovigilance is the science of detecting, assessing, and preventing adverse effects of medications. It's a vital aspect of the pharmaceutical industry that ensures patient safety and effective treatment. Why Pharmacovigilance Matters: 1.Patient Safety: Monitors and manages side effects. 2.Regulatory Compliance: Meets global health standards. 3. Continuous Improvement: Enhances drug formulations based on real-world data. 4. Trust and Transparency: Builds confidence among healthcare providers and patients. Key Activities: 👉 Collecting and analyzing data on adverse drug reactions. 👉 Reporting findings to regulatory bodies. 👉 Implementing measures to mitigate risks. #Pharmacovigilance #Pharma #PatientSafety #DrugSafety #Healthcare #RegulatoryAffairs #PharmaceuticalIndustry #LinkedInLearning
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Today, me and Laurent Vidal presented our innovative research and thoughts on the use of artificial intelligence for safety at the pronovea pharma summit. If you are curious to know more, stay tuned for our upcoming blog post!
Today is the day! Don't miss UBC's featured presentation at the Pronvea Pharma Summit on utilizing AI in routine pharmacovigilance activities. More info at https://hubs.ly/Q02tSMPq0 #PatientsFirst #Pharmacovigilance #DrugSafety #PatientSafety
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🌟 Ensuring Drug Safety Through Spontaneous ADR Reporting 🌟 Adverse Drug Reaction (ADR) reporting is vital for patient safety and public health. By leveraging spontaneous reporting systems, pharmaceutical companies and healthcare professionals can contribute to: 🔍 Data Acquisition: Reporting suspected ADRs to regulatory authorities like NPCs, CDSCOs, or AMCs. 📊 Data Assessment: Analyzing pooled international data for better insights. 📈 Data Interpretation: Identifying safety signals and improving drug safety protocols. At Croissance Clinical Research (CCR) , we encourage collaboration across the pharma industry to strengthen pharmacovigilance practices for a safer healthcare ecosystem. #Pharmacovigilance #DrugSafety #ADRReporting #PharmaInnovation #CroissanceAfrica Satish Marukurthi
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