Clinical Trials
Nimble recruitment, minimal drop-out, and reliable reporting. These are the hallmarks of a successful clinical study. Healint brings clinical trials directly to patients wherever they are.
Healint's virtual clinical trial technology provides pharmaceutical leaders with a massive, engaged patient base via Healint's mobile tracking apps, which boasts over 2.8 million users worldwide. These profiles can be used to create customised, bespoke cohorts of patients who experience specific symptoms that can be easily fine-tuned to suit a specific trial.
We can help you with…?
Patient recruitment
Feasibility study
e-PRO
Faster, high-quality patient recruitment
Ability to easily segment and refine your target demographic to find potential participants; we expand your geographic reach, providing access to diverse populations and difficult-to-recruit candidates.
How to assess the feasibility of your studies?
We help you uncover the strengths and weaknesses of your study, by providing comprehensive data, either for historical background or through out surveys
Electronic Patient-Reported Outcomes
Our intuitive, easy to use e-PRO delivers higher adherence rates. We have moved the clinical trials to a virtual setting and eliminate the need for in-person patient or nurse visits, cumbersome paper records, and armies of clinical research associates that monitor the accuracy of patient data.
Why us?
High focus on quality and patient safety
By performing virtual clinical trials, we help world pharmaceutical leaders reduce variation in data collection and provide near real-time data to enhance safety signal detection.
Faster, user-friendly, and more cost-effective trials
Digitally enabled workflows and engagement platforms simplify clinical trial processes leading to fewer errors and shorter timelines. Using mHealth technology can help you complete trials more efficiently and allow you to bring new therapies to market in a faster and more cost-effective manner.
Compliance 21 CFR Part 11
All electronic data points collected by Healint are reliable. We can ensure the authenticity, integrity, and confidentiality of our users and data recorded. These rules and regulations help to ensure robust and reliable Study. We are compliant with 21 CFR Part 11.
Standard Operating Procedure (SOP)
We gather a list of tasks and organize them into chronological steps. We support you during the design of the study protocol, and SOPs are used to cover all aspects of the data collection process.
Data integration
We also provide clean data output either to your preferred EDC platform (Medidata, IBM CD), merging our patient journey with traditional onsite eCRF, or directly into SAS for your statistical analysis.
Clinical research is not the practice of medicine but the collection of information about this practice
To collect the best data with the best patient engagement and the highest adherence, we design the best in-class platform.
A few screenshots… (please keep in mind this is just a screen sample, more are available and all are customisable)
Medication intakes
Events
Symptoms
Pain scales
Triggers
Relief methods
Let’s have a look at the competition…
| Capabilities | Medidata/ IBM CD/ other | Healint | Study specific platform * |
|---|---|---|---|
| Proof tested by millions of users | V | ||
| Secure data servers in multiple countries | V | V | |
| 21 CFR Part 11 Compliance | V | V | Rarely |
| Daily tracker - Clinical questionnaires | V | V | V |
| Multi languages interface | V | V | Rarely |
| Secure and private access | V | V | V |
| Dictionaries** | V | V | |
| Data quality & Process | |||
| Protocol - SAP - DMP Design | Option | ||
| User experience leading to best-in-class adherence | V | ||
| Inteligent reminders & Drop-out prediction | V | ||
| Recruitment Accelerator Service | Option |
*Dedicated app (Built by a CRO or 3rd party)
** Dictionaries (MedDRA, WHODrug)
