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Patient Protocol offers extensive expertise in clinical design and value strategy and uses program adaptation to benefit new technologies in our product development. Patient Protocol is rooted in expert consulting based on clinical trial design, data collection analysis and statistics, and gainful lessons learned that has proven to be transferable to other therapies and disease areas.
Patient Protocol makes our cross-platform system customized specifically to your clinical data collection needs based on our clinical analysis. We create distinctive need assessments and recommendations in the critical step of designing an accurate and reliable data collection platform.
Patient Protocol provides data-reliability, accuracy and an exceptional opportunity for data gathering in a progressive format that shall benefit your pipeline development and essentially create enhanced outcomes that could lead to better drugs to the market faster and at a lower rate.
Patient Protocol focuses solely on your specific needs and the needs of your patients. We provide best in class client support and we are able to adapt our service offerings to your requirements.
Patient Protocol is not just a technology cross-platform provider but rather a full-service company that understands your scientific needs and translates it into a targeted data collection technology system.
While it is possible to implement the Patient Protocol program at any stage of your clinical trial process, it is highly recommended that we are part of your early stage planning i.e. in the Clinical Trial Integrated Hub Setup during the clinical data management system (CDMS) process.
While it is beneficial to utilize the Patient Protocol program from the very early stages of a data collection program, it may never be too late to bring Patient Protocol into your process. Call us to discuss further so that we understand your unique situation and can present you with the best possible solution tailored specifically to your needs.
Phone: +1 203-400-7110
19 out of every 20 clinical trials fail*. It is an astonishing number and one that cost the pharmaceutical industry and therefore its patients billions of dollars. Outside the safety and efficacy considerations, poor data collection through difficult tracking tools (e.g. paper tracking) can be to blame. It is important to create a data collection system that provides an easy way of tracking progress, clear instructions, and encourages patient adherence. Excessive instructions, complicated onboarding and tracking tool instructions may weaken your chances of getting the data and results you seek. Patient Protocol uses a cross-platform where the technology drives the behavior. It is easy to use and patient adherence is of highest priority.
*The University of Texas MD Anderson Cancer Centert: spring 2012:
Patient Protocol is a full-service data collection provider and can assist you with patient adherence and maintenance programs as well as clinical trials and any other data collection projects. Since we tailor every data collection project to your specific needs there are no real limitations to how you can use our system.
While we have already built, tested, and debugged our technology and therefore save a lot of time in the process of customizing the build for your specific initiative, it is important to note that we tailor each and every program specifically to the independent project. No 2 projects are completely alike and it is therefore important that we identify the absolute best way to capture your data in your tailored program.
Since we tailor every data collection project to your specific needs there are no real limitations to how you can use our system or how many services you can add to the scope of work. See our case studies for examples.
Our program is very advanced and we are continuously improving our technology. We have already added the capabilities of taking photos and recording video and sound. These features can be used in your data collection initiatives.
Yes. Using our program you can currently observe data through the smartphone (iOS and Android), tablets and your computer. All the data feeds into a designated, patient specific cloud server and forwards to a live dashboard for your instant viewing advantage.
While we have already built, tested, and debugged our technology and therefore save a lot of time in the process of customizing the build for your specific initiative, it is important to note that we tailor each and every program specifically to the independent project. The timeframe varies pending to the level of customization required. Some platforms can take just a few weeks, some can take a couple of months.
No matter where your data collection is captured (smartphone, tablet or computer), it is automatically stored on an independent cloud server with maximum data safety. This data feeds into a live dashboard that you and your team will have access to remotely. The dashboard will display the captured data instantly. This means the minute data is entered, it is viewable on your end and can be analyzed immediately.
Please contact the Patient Protocol team for a non-binding evaluation specific to your data collection needs.
Contact the Patient Protocol team for more information about our program, services, and customization options.
Patient Protocol and the Mymee technology is used among pharmaceutical companies, university hospitals, CROs, and other research organizations as well as physicians and individual patients. Pending on your data collection needs, we tailor our technology specifically to your independent needs. For case studies please check here
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