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Expertise in CRO Rescue Services

Get Back on Track to Create a Healthier World

Pharm-Olam Pharm-Olam

Rescue Study Services

When your study is in trouble, finding the right team to mitigate complex challenges is vital to a successful outcome effectively. We have rescued more than 100 clinical trials by creating flexible solutions that bring your study back into balance.

Our experience includes studies in phases 1 through 4 across a range of therapeutic areas. In the last five years alone, we have rescued studies in various therapeutic areas, including disease, dermatology, hematology, nephrology, neurology, and oncology.

Because our corporate structure allows for increased flexibility and efficiency, we can follow your SOPs, provide our own, or create a new combination to accommodate your study. We will create a rescue study or trial optimization plan that meets your clinical trial needs. Our scalable and customizable solutions cover:

By providing expert experience and flexible solutions, we are equipped to work seamlessly with your teams or incumbent CRO to resolve clinical trial issues and help you reach important milestones and goals.


Therapeutic Expertise That Supports Your Study

Pharm-Olam’s therapeutic areas of focus have been built to provide an ecosystem of cross-functional, therapeutically-aligned teams. This strategy helps create synergies and efficiencies that ensure your rescue study or trial optimization solutions are optimally positioned to help your clinical trial reach its goals and milestones. 

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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

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Rescue Sponsor Testimonial

"When sites identified by other CROs struggled to identify qualified patients, we brought Pharm-Olam into the study to supplement enrollment and limit the damage of slipping timelines.  Now that the studies are complete, we are very impressed with the metrics that Pharm-Olam achieved in terms of study start-up, enrollment and database lock.  I would strongly recommend Pharm-Olam for future projects and look forward to working with the team again!"

Biotech - VP, Project Management

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Find out how our experts can help to rescue your study.

Talk with our team today.