Health Apps can solve these problems but building Health Apps is hard.
Expensive
Costs on average $425,000 to build as it requires an interdisciplinary team, a secure storage solution for patient data and a medical-grade infrastructure.
Time-consuming
Takes on average 15 months as it's a highly-regulated industry. Stringent security, medical device regulation, and ethics review need to be taken into consideration.
Poor User Engagement
Health apps are often so badly designed, leading to poor user engagement. Over 50% of health apps see a usage drop-off rate of 64% after just 30 days.
The Patient receives a clinic-branded companion mobile application that helps businesses in a variety of medical fields to improve the patient experience, from the initial point of contact to long-term follow-up.
Personlised Care Plans
Smart Surveys
Wearable Integration & Physical Assessments (e.g. 6 min walk test)
Co-develop. Engage. Incentivize. Monitor. Optimise. Deliver a better patient experience.
The clinic accesses Zendra's Admin Dashboard to customize versions of the Patient App for both iOS and Android.
The Admin Dashboard is a software application that allows businesses in a variety of medical fields to configure and monitor the Patient App for its patients.
App Builder
Care Plan Management
Telehealth
Patient & Care Team Management
Analytics
Marketing Campaign Management
Highly-interoperable. Designed to seamlessly integrate with healthcare systems.
Rest Assured that our platform will integrate in nicely to your existing Health Systems.
All Health Data in our platform is stored using the highly-interoperable HL7® FHIR® standard.
Medical-grade. Built for medical device classification.
Patient safety comes first. Unlike 98% of software companies worldwide, Zendra implements medical-grade Quality Assurance on all our processes, procedures, and Usability Engineering to ensure your product meets it's Intended Use.
Zendra carefully selects Suppliers and tools upon undertaking stringent vetting and validation.
Zendra is compliant with medical device regulatory standards ISO 13485:2016, IEC/DIS 62304:2018 and 21 CFR Part 11 compliance.
Zendra Health provides quality records and regulatory documents as part of each project deliverable which can be leveraged by clients for medical device classification of a digital therapeutic.
Secure-by-design infrastructure.
Security is paramount in any software business, particularly when it comes to storing patient data.
Zendra Health’s data store is GDPR & HIPAA compliant and uses best-in-class security measures for storing personal health information.
All server communication is encrypted over TLS and data is encrypted on REST.
Our platform securely stores patient data so you can concentrate on what matters most, delivering better outcomes for your patients and your clinic.
Our platform has a broad range of medical-grade building blocks to cater for your digital therapeutic needs.
Patient View
Engage. Incentivise. Improve health outcomes.
The Patient receives a clinic-branded companion mobile application that helps businesses in a variety of medical fields to improve the patient experience, from the initial point of contact to long-term follow-up.
Co-develop. Engage. Incentivize. Monitor. Optimise. Deliver a better patient experience.
The clinic accesses Zendra's Admin Dashboard to customize versions of the Patient App for both iOS and Android.
App Builder
Care Plan Management
Telehealth
Patient & Care Team Management
Analytics
Marketing Campaign Management
Interoperability
Highly-interoperable. Designed to seamlessly integrate with healthcare systems.
Rest Assured that our platform will integrate in nicely to your existing Health Systems.
All Health Data in our platform is stored using the highly-interoperable HL7® FHIR® standard.
Regulatory
Medical-grade. Built for medical device classification.
Patient safety comes first. Unlike 98% of software companies worldwide, Zendra implements medical-grade Quality Assurance on all our processes, procedures, and Usability Engineering to ensure your product meets it's Intended Use.
Zendra carefully selects Suppliers and tools upon undertaking stringent vetting and validation.
Zendra is compliant with medical device regulatory standards ISO 13485:2016, IEC/DIS 62304:2018 and 21 CFR Part 11 compliance.
Zendra Health provides quality records and regulatory documents as part of each project deliverable which can be leveraged by clients for medical device classification of a digital therapeutic.
Security
Secure-by-design infrastructure.
Security is paramount in any software business, particularly when it comes to storing patient data.
Zendra Health’s data store is GDPR & HIPAA compliant and uses best-in-class security measures for storing personal health information.
All server communication is encrypted over TLS and data is encrypted on REST.
Our platform securely stores patient data so you can concentrate on what matters most, delivering better outcomes for your patients and your clinic.
How it works - in 4 simple steps
Step 1 - Design
Co-Design
Being a medical-grade software provider, Zendra Health takes User Experience Design seriously.
At Zendra, we collaborate with our clients in designing and wireframing the Digital Therapuetic to ensure it's optimised for your care pathway.
Step 2 - Build
Choose your template
The Zendra Health platform's Admin Dashboard provides persona-driven templates to facilitate rapid medical-grade app development that is suitable for a wide variety of medical fields.
Add your content
Swiftly build your Health App using a broad range of building blocks provided on the Zendra Health platform.
Feedback from key stakeholders on your Health App can be instantly updated through the Admin Dashboard.
Step 3 - Launch
Training
Zendra Health are firm believers that a digital health solution should fit seamlessly into our client's workflow.
Zendra Health help with training and marketing materials to ease the onboarding process of the Health App in your clinic.
Publish
Zendra handles the publishing of the Health App.
Regulation
Given our platform is compliant with medical device regulatory standards ISO 13485:2016 and IEC 62304:2018, we can provide the medical device history records as part of the project deliverable which you can leverage for medical device classification.
Step 4 - INSIGHTS
GAIN INSIGHTS
Use Zendra's Admin Dashboard to gain visibility of patient progress outside the four walls of a clinic and track patient app engagement and referrals.
Customers
We work with world-renowned healthcare institutions and industry-leaders in Pharma and MedTech.
Healthcare
Enhance a patient journey by providing them with personalised care on their mobile phone.
Pharma
Accelerate Drug Development by building a mobile-based companion study for Phase II-IV clinical trials.
MedTech
Provide a more holistic care offering by providing a companion app for your medical device.