Standardizing and improving safety surveillance with Vigilance Workbench
A top 10 pharma company faced challenges in standardizing safety surveillance across Pharma, Vaccine, and Consumer Health units, including consolidating signal teams, facilitating a divestment, integrating multiple data sources, migrating data from legacy systems, replacing existing methods, and simplifying the IT landscape. The timely deployment of Qinecsa’s Vigilance Workbench significantly benefited the client by increasing […]
Integrating Medical Devices into Pharmacovigilance Portfolios
In her latest article for IPI, Qinecsa President, Humaira Qureshi discussed the practical challenges of integrating medical devices into pharmacovigilance portfolios, the obligations of device manufacturers, how to navigate the European Medical Device Regulation, maintaining effective post-market surveillance and managing the life cycle of a medical device. Understanding medical device regulations is essential for pharmacovigilance […]
Qinecsa featured in International Pharmaceutical Industry (IPI) editorial
In her latest article for IPI, Qinecsa President, Humaira Qureshi, addresses the practical challenges of integrating medical devices into pharmacovigilance portfolios. She explores the obligations of device manufacturers and offers insights on navigating the complexities of the European Medical Device Regulation (EU MDR). “Understanding medical device regulations is essential for pharmacovigilance professionals seeking to master […]
Shaping the Future of Clinical Research Technology
A head of our first exhibition at the DIA Global Annual Meeting, taking place in San Diego from June 16th-20th, Qinecsa spoke with Outsourcing-Pharma about our latest breakthrough in clinical research technology, how it addresses the current challenges in the industry, and the major trends that will shape the future of pharmaceuticals. You can read the […]
Embracing a new future-ready pharmacovigilance ecosystem
Following her attendance at DIA Europe 2024, Humaira Qureshi, President of Qinecsa Solutions, spoke with PharmaPhorum about the transforming pharmacovigilance landscape, the potential barriers and how organizations can embrace a new future-ready pharmacovigilance ecosystem. “This offers an opportunity to embrace novel technologies, aligned with culture and processes, to demonstrate how pharmacovigilance (PV) can save time, […]
Join Qinecsa at the Insife Annual Convention 2024
We are thrilled to announce that Humaira Qureshi, President of Qinecsa, will be a keynote speaker at the upcoming Insife Annual Convention 2024. The event is scheduled to take place on the 26th of September at the Novartis Campus in Basel, Switzerland. This convention serves as a premier gathering for pharmacovigilance professionals to explore the […]
Qinecsa shares latest innovations with industry media before DIA Global Annual Meeting 2024
Ahead of exhibiting at the 2024 DIA Global Annual Meeting, Qinecsa spoke with industry leading journal Outsourcing Pharma about the company’s latest breakthrough in clinical research technology, how it addresses the current challenges in the industry, and the major trends that will shape the future of pharmaceuticals. Qinecsa discusses the vast volumes of data and […]
Vigilance Medical Device Guidance – Part 2: Reporting Essentials and Obligations
Webinar: Vigilance Medical Device Guidance – Part 2 Post-Marketing Safety Surveillance of Medical Devices and DDC Products, EU and USA Join us for Part 2 of our webinar series on post-marketing safety surveillance, where we dive deeper into the intricate world of medical devices and drug-device combination products. Building upon the foundation set in Part […]
Join Qinecsa at DIA Global Annual Meeting 2024
Qinecsa is thrilled to announce exhibiting at the DIA Global Annual Meeting, happening from June 16th to 20th in San Diego, CA. Redefining Healthcare through Innovation and Collaboration DIA is the largest multidisciplinary event that brings together a global network of life sciences professionals. The meeting fosters meaningful innovation that will lead to the development […]
Qinecsa releases on-demand webinar on mastering Medical Device regulations
On April 17, 2024, Qinecsa launched its first webinar, offering a deep dive into medical device regulations. The on-demand session, “Mastering Medical Device Regulations (EU) 2017/745,” is designed for pharmacovigilance professionals aiming to excel in compliance and operational effectiveness. The 50-minute webinar offers a thorough analysis of the latest EU medical device regulatory landscape, providing […]
