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Clinical Trial Feasibility Services

Optimize Your Study Decisions Through In-Depth Site Feasibility; Setting You on the Path Towards Creating a Healthier World.

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The clinical trial space is inherently complex and becoming even more competitive, depending on the disease and the geography you’re considering for your clinical trial. Pharm-Olam’s clinical trial site feasibility studies provide you with an invaluable understanding of the current dynamics. Our feasibility reports give you in-depth feedback, so you have a complete picture of what’s happening on the ground in your disease of interest.

No longer is it sufficient to have just site-level responses when conducting your feasibility. We examine internal and external datasets, evaluate incident and prevalence data, and run the due diligence all while measuring and analyzing the competitive landscape. In addition to historical benchmarking, we pull in feedback from subject matter experts. This information is then analyzed and compiled into a report that provides you a realistic and comprehensive outlook on the landscape for your trial.

By relying on Pharm-Olam’s holistic approach, you can optimize feasibility, site identification, and selection, allow you to enroll sooner and start your studies faster. Our global feasibility and site solutions team is poised to support your efforts to optimize your study.

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Gain a Detailed Analysis Customized For Your Needs

With collaboration from our medical and operations teams, we review your study design and protocol and can give you guidance about feasibility at whatever stage you are in. At the pre-award phase, we will conduct a blinded, complimentary feasibility study with in-depth analysis and data to support our continued joint discussions and preparations for your project.

Pre-study feasibility evaluations can be especially beneficial, particularly if you will be conducting a rare disease trial. We’ll develop customized questionnaires to ensure we derive the information you require. Post-award, our experts can provide support with GDPR, navigating the privacy notices for investigators and staff. We will tailor our work based on your needs, budget, and the complexity of your study.

On an expedited timeline? Our team will work with you to maximize the value of your feasibility study in your timeline.

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Global Execution, Local Knowledge. Reaching Your Targeted Investigators.

Study startup at multiple sites is complex but becomes even more so unless you have in-depth knowledge about each of those sites and locations. This is an area in which we excel. Operating in 60+ countries, we tap into the local knowledge of our country managers, who are an integral part of our feasibility group. With their on-the-ground expertise and knowledge, we bring you insight impossible to obtain from afar.

Besides knowing the language, customs, and regulatory environment, our dedicated local teams can tap into the local investigators and key opinion leaders while assisting with the execution of the feasibility study and supporting and following up with sites.

We also deploy a digital survey tool to directly reach out to our sites, engaging and collecting real-time responses from investigators and their staff globally. Using an array of sophisticated tools to collect and analyze the data, we also tap into our medical, regulatory, and study team experts to ensure we gather a complete picture for your upcoming study.

More so than any other CRO, our approach to clinical trial site feasibility conduct is customer-service-oriented. With a personal touch, we foster a true partnership with you. We want to consult with you, offering you customer service support and answering your questions in full.

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Need Questions About Study Design or Sites Answered?

Our team of feasibility experts can help prepare you and your study for success. 

Talk with our team today.