Frequently asked questions

Human factors (or usability) studies are intended to demonstrate the performance of a device or medical product whilst remaining within an environment that simulates its real environment of use and by the variety of people who are potential users. A well-designed study will identify any safety or application problems. It can include user interaction with devices, systems, software, apps, and instructions for use. Stringent regulations ensure participant protection and ethical conduct throughout evaluations, maintaining the highest standards of research integrity.

All medical device studies encompass a diverse range of conditions and subject matters, welcoming participants of all backgrounds. When you register with Aderico Medical, you join our candidate database, and we carefully match you against the set recruitment criteria. We're constantly looking to expand our volunteer pool, so please consider sharing our opportunities with your friends and family—your recommendations mean a lot to us!

Upon registering with Aderico Medical, your information is securely stored in our database. If you match a study, our recruitment team will contact you, provide study details, and confirm your eligibility. You may need to complete a screening form. Once you agree to participate, we'll share study specifics and a scheduling link. Our team is available to assist and answer your questions, ensuring your comfort throughout the process.

For the most part, our medical device evaluations are conducted in person at a designated location. This approach allows our clients to seamlessly conduct consecutive sessions in a controlled environment, typically within a specially arranged viewing space tailored for such studies. However, we also recruit for remote studies that can occur at a participant's residence (or workplace for healthcare professionals). The feasibility of remote studies depends on the specific study requirements and the type of participants needed

The duration of study sessions varies based on the unique requirements and criteria of each study. Normally, a session can last anywhere from 1 to 3 hours. However, in some cases, studies may encompass several hours, extend over multiple days, or even span across several months to achieve completion.

The majority of our research studies depend on the valuable contributions of volunteers to advance the development of device usability. We offer a compensation package to participants to cover travel expenses and time commitment required for the study. The recruitment team will provide you with detailed information regarding the specific financial reimbursements available, as these can vary depending on the particulars of each study.

Incentive fees and travel expenses are typically disbursed through direct bank transfers, with payments usually processed within three business days following the completion of the study. Our recruitment team will securely collect your bank details during the recruitment process, typically in the days leading up to your scheduled study session. To prioritize security, this information is gathered over the phone, and it's important to note that we do not retain or store your bank details.

Yes, We have a growing cohort of participants who generously contribute their time to engage in various studies regularly. However, to maintain impartiality, we restrict participation in studies with similar product types. As a general guideline, participants are typically ineligible if they have taken part in a comparable study within the past 3-6 months.

If you find yourself unwell on the day of the study, it's crucial to notify our team promptly. We are committed to providing the precise number of participants required for each study, and it's essential that all scheduled participants are available. In exceptional situations where a participant cannot attend, informing our recruitment team immediately is vital. We maintain a pool of backup participants who can step in on short notice to ensure the study proceeds as planned in such circumstances. Your prompt communication helps us maintain the study's integrity and meet our contractual obligations.

At present, we do not have the capability to share the results of individual studies with participants, primarily due to client confidentiality and sponsor-imposed restrictions. Some studies span over several years, making it challenging to adhere to specific publication timelines. Nevertheless, please know that your contribution to advancing healthcare is invaluable and greatly appreciated.