Case Management & ICSR Processing

Case Management & ICSR Processing

Case Management & ICSR Processing

Veram Bioclinical Solutions specializes in Case Management and Individual Case Safety Report (ICSR) Processing, crucial for ensuring the safety of pharmaceutical products. Our services cover the entire process, from case intake and triaging to data entry, coding, and writing narratives. We use standardized dictionaries like MedDRA to ensure accuracy and consistency in coding, and we conduct causality and labelling assessments to evaluate the impact of adverse events.

Our team excels in quality and medical reviews, ensuring that all adverse event reports meet regulatory standards and best practices. We are proficient in expedited reporting to regulatory authorities, ensuring that safety information is reported in a timely manner. Veram Bioclinical Solutions' expertise in case management and ICSR processing ensures that our clients can trust us to handle their pharmacovigilance needs with precision and efficiency, ultimately contributing to the safety of patients using pharmaceutical products.

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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.