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 is certified to medical device regulatory standard ISO 13485:2016, and compliant with software development standards for medical-grade software IEC 62304 and 21 CFR Part 11.

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

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