Nina Koshik is an experienced quality management professional with a strong background in drug safety monitoring and research. Currently serving as Quality Manager at PV.app since June 2023, Nina has previously held roles such as Quality Assurance Specialist at Eisai EMEA and Quality Specialist at Elanco, where significant contributions included developing standard operating procedures, managing audits, and implementing quality assurance systems. Nina's career began at Fisher Clinical Services with dual roles as Quality Specialist and Associate Project Manager, overseeing IT system projects and supplier partnerships. Additionally, Nina's foundation in pharmacy was established with a Master's degree from Samara State Medical University, complemented by further education in design and applied arts through Coursera and the British Higher School of Art and Design.
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PV.app - Patient Safety Monitoring & Research
🧬 Life Science is more than a business sector; it’s the cornerstone of human health - the base and source of innovation. Even with healthcare being so crucial, it’s impossible to rest knowing the industry still grapples with challenges and limitations. In response to this injustice, a team of passionate software engineers and pharmaceutical professionals from across the globe joined forces. We have founded Genira, established in the vibrant city of Singapore.🇸🇬 Our commitment is to bring cutting-edge user experience and technological advancements to all healthcare professionals who strive daily to save lives and improve patient well-being. Addressing the demands of modern pharmacovigilance head-on, where over 60% of cases are under-reported and manual processes still dominate, we created PV.app. PV.app is an AI-powered cloud solution that simplifies the case intake for pharmaceutical companies, biotechs, and CROs, leading to increased reporting rates and improved safety compliance. Leveraging machine-learning techniques and adhering strictly to international standards, PV.app becomes a powerful tool for all safety studies, offering: ⏱️ Speed in detecting emerging safety issues and initiating studies 🧘 Efficiency by reducing team workload for case processing 📈 Cost-Effectiveness as an all-in-one solution for data collection, analysis, and reporting 👉Join the PV.app revolution - for a safer, smarter, and more efficient approach to pharmaceutical safety surveillance. Send the request for a demo and get early access to our new features: https://www.pv.app/#contact