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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 professionals, and researchers. Here is […]
Pharmacovigilance, an integral field within the realm of drug safety, encompasses a wide range of activities that aim to monitor, assess, and prevent adverse effects associated with medications. By undertaking these endeavors, pharmacovigilance ensures that the benefits provided by a […]
Clinical trials happen in several phases during which different questions are asked.
Each phase builds on the results of previous phases
Are you navigating the complex world of regulatory compliance? Look no further! Our Regulatory Affairs Services Company is here to guide you through the ever-changing landscape of regulations, ensuring your products meet the highest standards.
From breakthrough discoveries to cutting-edge technologies, medical research continually uncovers new insights and transforms the way we approach healthcare.
Case Study An India based manufacturer, focused on Branded Formulations, Specialty Generic Injectables, Synthetic Biology, Vaccines and Biologics At A Glance Challenges Medical Inquiries Product Complaints Adverse Drug Experience Reporting Other Categories Combination of the above calls. Highlights 2600+ Aggregate […]
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
Vigilare Biopharma is attending the 9th edition of the PharmaLytica expo which is held from 01 – 03 June 2023 at HITEX, Hyderabad, PharmaLytica 2023 is evolving as the leading expo for products and services along the entire value chain […]
