SITE MANAGEMENT

If you're looking to harness the full potential of a Site Management outfit for your clinical trials, ERD is your ideal partner.  In addition to our role as intermediaries, we also provide comprehensive support and assistance throughout the entire clinical trial process. From identifying suitable trial sites to managing regulatory compliance. One of the main functions of ERD is to identify and select appropriate clinical trial sites. This involves conducting feasibility studies to evaluate the site's capabilities, patient population, infrastructure, and compliance with regulatory requirements. ERD uses their networks and databases to match trial protocols with the most suitable sites, ensuring optimal trial execution. ERD act as intermediaries between researchers, sponsors, and trial sites, facilitating seamless collaboration and coordination. We bring a wealth of expertise and experience to the table, ensuring that trials are conducted efficiently and effectively. Efficient site management is essential to ensure that clinical studies run smoothly and result in best outcomes. Selecting sites as per the study protocol and the applicable regulatory requirements can positively impact on the quality of data collected and ensure that the study is conducted as per the agreed timelines and within budgets.