As a leader in Pharmacovigilance Processes, we offer end-to-end services to ensure the safety and efficacy of pharmaceutical products. Our expertise includes setting up and implementing robust pharmacovigilance systems, including the preparation and maintenance of the Pharmacovigilance System Master File (PSMF) and SOPs. We provide consultancy services and project management to guide clients through regulatory requirements and best practices, ensuring compliance and patient safety.
Our comprehensive case management and Individual Case Safety Report (ICSR) processing services cover everything from case intake and triaging to data entry, coding, and writing narratives. We conduct causality and labeling assessments, along with quality and medical reviews, to ensure all safety information is managed efficiently and in compliance with regulations. Veram Bioclinical Solutions excels in expedited reporting to regulatory authorities, ensuring timely and accurate reporting of safety information.
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[email protected]Ready to elevate your clinical trial or pharmacovigilance process? Contact Veram Bioclinical Solutions today to discuss your needs and discover how our expertise can benefit your organization.