As a full-service CRO, Pharm-Olam offers a complete suite of services to match the individual requirements of today’s complex clinical trials process. From the simplest communication protocols that ensure secure, timely, collaborative channels of communication to the most complex, multi-national development programs, Pharm-Olam can tailor solutions that meet your budget and complement your internal resources.
Our full service offerings are international with Regulatory, Clinical, and Project Management services offered across the majority of our 40 countries. In addition we offer Medical Writing, Data Management, Biostatisticians, Pharmacovigilance, and Medical Monitoring services from North America, Europe and India. With Pharm-Olam’s extensive and varied study history, you can be sure that we have worked on a study program similar to your ongoing study programs. With over 80 physicians on staff, Pharm-Olam has full-time, in-house experts who are available to consult and participate in your study, ensuring the highest-quality results available.
"Turnaround timelines for actions were consistently achieved and Pharm-Olam's constant communication with the global teams and vendors resulted in a smooth execution of study and on-site activities."
- Associate Director, Clinical Operations
Pharm-Olam also has outstanding and proven relationships with sites and investigators located around the globe. These relationships ensure that we can work together to create a sound study protocol and subsequently ensure that accurate study results are collected and reported back to you, on time and within budget.