The CRFG is committed to providing high quality Pharmacovigilance / Device vigilance services. Our systems are designed with protection of participant safety and regulatory compliance at their core. We provide a bespoke Pharmacovigilance service and support throughout the life cycle of the study.  Our Pharmacovigilance / Device vigilance services conform to the relevant regulatory requirements and guidelines in conjunction with CRFG Standard Operating Procedures. The CRFG Pharmacovigilance services can be used as a standalone service or integrated into the wider multidisciplinary study team. This integration, in particular with the Data Management services provides a seamless, efficient and effective service, at both the study site and sponsor level.