Rescue study process
Proven Rescue Study Processes and Solutions
When issues like delayed enrollment, postponed timelines, budget problems, regulatory issues, and resource constraints threaten to derail your research, Pharm-Olam’s rescue services can help get your study back on track.
Our rescue study services team can quickly analyze your study’s needs and design customized solutions to get your clinical trial moving in the right direction.
Your official transition plan will be initiated by experts from specialized areas who work in parallel to execute regulatory approvals, site agreements, and logistical requirements. They also work to build productive relationships that better position your clinical trial for success in the future, setting your study on a course for continued success.
Whether you need additional sites in an active country, sites in new countries, or want to transfer an ongoing study, we can help you meet your enrollment needs. Since slow recruitment is the number one clinical trial issue, we have a rescue startup team that analyzes your enrollment options rapidly. We also provide you with a global network and decentralized monitoring model that allows us to quickly initiate sites in countries with higher recruitment rates than the U.S. or Western Europe.
Our proven processes and solutions are designed to improve communication between all teams to alleviate future study issues before they arise and put your clinical study on the road to success.
Are you looking for assistance on how to plan and execute a rescue scenario? Watch our on-demand webinar - Rescue Your Study: A Sponsor’s Playbook.
Rescue Playbook Webinar