Experience the rare joy of early enrollment
Patient enrollment is the single biggest risk to clinical trial timelines and budgets. We have built a reputation turning enrollment failures into successes and we lead the industry in recruitment results. With Biorasi, you can leverage a legacy of expertise, innovative and effective approaches to patient recruitment.
A patient-centric process designed to accelerate patient identification, engagement, and enrollment.
Recruitment starts with identifying where your patients are and who they are seeing for their condition. Traditional CROs use a site-centric approach to patient identification, relying too much on outdated experience and questionnaire-based feasibility inquiries that are rarely accurate.
At Biorasi, we do it all differently from the start. We understand that each indication, protocol, and indeed each patient, is unique. Rather than focusing solely on sites, we begin with understanding as much as possible about the patient experience, and then we help you to design and execute a recruitment strategy that is tailored to those patients.
We have the agility and flexibility that is necessary to find the most challenging patient populations, leveraging a powerful identification toolkit featuring the best the industry has to offer:
Global Site Networks
Tap into our growing network of private clinics, renowned hospitals, institutions, and key opinion leaders around the world.
Some countries and institutions keep track of different patient populations via a registry. For many difficult-to-recruit conditions, these registries can be key to our recruitment strategy.
Biorasi partners with public and private payers with access to a wide range of clinical data – from diagnostic criteria to procedure and medication information – that we can leverage to identify exactly where your target population is.
Electronic Medical Record (EMR) systems are often shared between sites across sometimes diverse geographical regions, providing a more efficient way to identify patients than via individual sites alone.
We partner with the largest laboratories across the globe, tapping into a wealth of real-time diagnostic data that can be used to identify potential providers and patients.
We work directly with the patient community leaders to establish a direct line with individual patients, accelerating patient identification, education and engagement.
We understand that it is one thing to identify a patient for your study, and a totally different thing to get that patient to show up for a screening visit. That is why we have resources and processes devoted specifically to help engage and educate potential participants and facilitate their transition into the clinic for screening.
Our experienced web developers can launch an eye catching and informative study website in a matter of weeks.
Our dedicated marketing team can create and manage ad campaigns tailored for your patient population and targeted to specific geographies and mediums, including print, radio, digital and social media.
We take a community engagement approach, covering local and regional events where your patients and their caregivers will be looking to find out what new treatment options are available.
Advocacy Groups and Foundations
Biorasi partners with the patient community and its leaders in order to give your study better visibility, help to educate patients and their caregivers, and provide opportunities for patients to engage with your content directly.
Our unique Patient Navigator group provides a white-glove service including patient and caregiver direct contact, pre-screening based on study specific criteria, and coordination with sites or home nurses for screening and enrollment visits – increasing screening rates and accelerating enrollment.
Our recruitment results speak for themselves. When pitted side-by-side with other CROs in the same studies, Biorasi 8x faster.