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Quotient has the experience & expertise to seamlessly deliver your studies with the highest quality service & speed to clinical data. If you need a complete service including data analysis, subject recruitment, medical writing, Quotient is your answer.

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We develop study-specific retention plans when needed but our main retention strategy for all studies is to maintain close interaction with both patients and the primary care provider. We ensure patients feel valued, are kept informed.

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When you place a study with Spaulding Clinical Research you have access to a team of recruitment experts, who are dedicated to enrolling participants for your study. Our recruitment metrics show that our team delivers and they do it on budget.

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Traditional methods of increasing enrollment are expensive and inefficient. SubjectWell’s recruitment marketplace helps you find the right candidates faster so you can stay on schedule, avoid risky spending on recruitment, and get to market faster.

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Our team focuses on narrowing the gap between patients and clinical research by reaching out to physicians and their patients and helping them participate in clinical trials.

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We understand potential obstacles to recruitment and recognize the importance of a well-outlined recruitment and retention plan developed in conjunction with the study protocol.

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SubjectWell continuously engages the 96% of Americans who have never participated in a clinical trial. We are already talking to patients near your site who are looking for studies and have relevant health conditions.

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Optimize study power and achieve maximum enrollment, retention and compliance with our patient-centric design, tailored patient outreach and automated BYOD technology.

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To determine the safety of topical products, RCTS provides a range of clinical testing procedures, including a broad range of in-use and patch studies. Determining product safety under normal or exaggerated use conditions.

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Patient-Centered Sciences combined services establish Mapi as the clear industry leader in supporting patients or their caregivers, and offer proven results for accelerated drug development, improved recruitment, increased patient engagement, excellence in patient-reported data, and minimized

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The Patient Engagement Plan places the patient at the centre of the clinical trial’s preparation and management. Each plan is different, tailored to the specific circumstances of the patient community within the chosen country.

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Traditional trial recruitment methods look for patients with a particular health condition who happen to live close to a specific clinical site. This is targeting a needle in a haystack. At SubjectWell, we engage the entire haystack – the 96% of people who have never participated in clinical

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On average, Celerion screens more than 2,300 subjects per month. This success rate is attributed to our experienced staff, our extensive recruiting efforts and our ability to understand both the study requirements and the local subject pool for each of our clinical facilities.

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Imagine an eConsent solution that improves compliance and consent accuracy and provides an IRB-integrated process that activates studies in days instead of weeks. Q Consent is the future of electronic informed consent and it’s available now for your research studies.

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Evidera’s patient-centered researchers represent a unique combination of scientific disciplines, including psychometrics, economics, decision analysis, epidemiology, biostatistics, psychology and public health.

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PAREXEL leverages over 30 years of clinical trials experience with a data-driven approach that integrates all drivers of effective clinical trial patient recruitment.

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We are counted on for swift and reliable clinical medicalndevice/IVD services by companies and clients from everyncorner of the globe.

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With a large global network of talented clinical research professionals and vast industry expertise, DZS provides recruiting services across a range of clinical development positions and locations.

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At TFS we strive to ensure costs are kept within the budget using our in-depth knowledge of international and local regulatory requirements and our network of global investigators to ensure that the trial objectives will be met on time.

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Participant enrollment is often the single largest cause of delays in clinical research and often accounts for one quarter of the clinical program timeline. Our team expedites this process by taking a strategic approach to clinical trial recruitment.

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TFS offers a proven process for rapid patient recruitment without compromising results. With access to a worldwide network of KOLs and investigational sites in a broad range of therapeutic areas TFS’ dedicated Recruitment Services Team handles every aspect of patient recruitment from placing

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The Clinical Data Management unit efficiently manages all aspects of data handling in accordance with the protocol, the data management plan, efficient data capture, accurate data and timely completion of the clinical database.