A French based research company were looking for guidance on developing a medical device to ensure MD safety validation. VCLS became an extension of their team, designing a comprehensive Clinical Study Management program which optimized the timeline to first-in-patient, ensuring full regulatory compliance along the way.
Taking the Pain out of Clinical Studies for Medical Devices
Within a rapidly evolving regulatory scene, medical devices are under high scrutiny. Regulatory requirements are currently being reinforced, in particular to ensure patient safety.