Our case processing workflow supports efficient ICSR processing
Med Communications provides high-quality pharmacovigilance support to our clients to ensure that all individual case safety reports (ICSRs) are processed in a timely and accurate manner, independently of the source.
When it comes to ICSR processing and submissions, we provide our clients a well-established, automated workflow for the management of their cases originating from various sources that include, but are not limited to, health care providers, patients, scientific literature, interventional and epidemiological studies, post-approval clinical/safety studies, registries, patient support programs, etc, which includes:
- Collection
- Processing
- Medical evaluation
- Single case reporting of adverse events
Our professional team of medical, pharmaceutical, and academic experts offer a broad range of expertise in case processing. We have experience working with multiple agencies including the Food and Drug Administration, European Medicines Agency, Medicines and Healthcare Products Regulatory Agency as well as others worldwide. This experience gives us the ability to reconcile with other non-PV functions such as medical information and the confidence to expand into new markets. Contact us today to learn how we can help you: 877-477-0977 or https://medcommunications.com/contact-us.
