Registries are quite important in clinical trials. Today, registries optimize patient care and safety by allowing another level of research once a product is approved in the market. They are considered a robust and reliable system that uses several methods to obtain critical data that are further used in effective clinical research. The research evaluates specific outcomes for a patient registry or population, which are further classified by a particular disease, condition, or exposure.
Modern medical technology such as patient registries and EDC systems for clinical trials are helping optimize patient care and safety. Let’s look at the different aspects of registries and how they can benefit clinical researchers and the patients under observation.
The Role of Registries in Clinical Research
Registries are playing a vital role in modern medical research. Registries can help researchers continuously monitor the effectiveness of new medical practice and serves to bridge the gap between clinical trials and clinical practice. Registries are responsible for forming effective studies that inspire therapeutic development and provide insights into patient care.
Clinical researchers can document and report patient-safety data not captured in clinical trials and, in return, improve the overall research process that ensures patient care and safety.
Identifying Useful Information
Registries also allow clinicians to identify and capture useful post-marketing information on medicines and new therapeutic procedures. Clinical researchers can gather useful information about any approved drugs’ adverse events or side effects. Many patient registries are optimized to provide patients with structured questionnaires to collect useful information. Clinicians can capture serious adverse events that require patient safety through the patients themselves or their caregivers.
Monitor Drug Safety
Another way registries can help clinicians is through drug safety monitoring. Registries are being extensively used to monitor the safety of FDA-approved medications by engaging clinician participation in risk minimization actions plans (RiskMAPs) or risk management programs (RMPs). You need to ensure that drugs are safe for use, and registries can help by providing you with crucial data through patient participation.
How Can ClinicalPURSUIT Help?
If you’re looking for efficient registries and state-of-the-art EDC systems to help you in your clinical trials, check out the products and services provided by ClinicalPURSUIT. We have been operating since 1998 and have established our reputation for providing effective and state-of-the-art patient registries and clinical trial data management solutions to CROs, sponsors, organizations, and researchers.
Our commitment to quality and the ability to go above and beyond for our clientele has led us to become one of the best providers of modern EDC technology. Our products and services offer the latest technology that is helping those involved with clinical research and trials with effective data collection and analyses.
ClinicalPURSUIT has always been focused on adding value for our clients. In addition to patient registry solutions, we also provide products and services such as Randomization and Drug Supply Management, Electronic Patient-Reported Outcome Software, Clinical Electronic Data Capture Software, and more.
Schedule a one-on-one free demo today to learn how our patient registry services can help your team.
