AMRC responds to an FDA consultation

As part of AMRC’s role to advocate for multisite clinical research corporations (MCRC), we responded to the FDA’s consultation: Protocol Deviations for Clinical Investigations of Drugs, Biological Products, and Devices; Guidance for Industry – Draft Guidance.

Operational inefficiency in clinical research: what is it costing Sponsors and CROs?

The Association of Multisite Research Corporations (AMRC) welcomes a panel of experts to discuss the financial and operational impact of inefficiency in clinical trials. We’ll be joined by representatives from regulatory, academic, pharma, and trial sites, who will share their perspectives on the challenges facing the industry and possible solutions to streamline trials, improve data quality, and bring therapies to patients faster.