We help Pharma companies accelerate their drug development.

Building companion apps for Phase II-IV clinicial trials can be challenging to do alone.

It requires:
  • An interdisciplinary team of project managers, software engineers, UX designers, medical, security and regulatory domain expertise.
  • Patient and clinician-centric design expertise.
  • In-depth experience in determining and executing the optimal solution rollout strategy.

We help Pharmaceutical companies and Contract Resource Organisations (CROs) reduce drug development costs by building patient-centric companion apps for Phase II-IV clinical trials that connects patients and clinical trial teams outside the four walls of a site.

Security and medical-grade regulation are ingrained in our DNA. Zendra Health is one of the select few companies worldwide that are compliant with medical device regulatory standards ISO 13485 and IEC 62304.

No matter where you are on your journey in 'moving beyond the pill', we are here to help.

Contact Us