Decentralized clinical trials

Transform clinical trials digitally to be future-ready

Ensuring that your clinical research can respond to market changes is possible with IQA’s prowess to decentralize clinical trials by including emerging technologies.

 IQA’s Decentralized Clinical Trials (DCT) solutions is aimed at enhancing clinical studies by infusing digital technologies and practices while keeping patients at the heart of it all.

Our solutions are designed to face any eventuality through flexible options of both virtual and hybrid trials to keep your patients engaged wherever they are. With IQA, you don’t just get an uninterrupted clinical study ecosystem, but also achieve success at low cost and with greater efficiency. Our DCT solutions extend across all our therapeutic areas.

Decentralized clinical trials have garnered a lot of attention for the benefits it presents and ease of operations. But implementing DCT requires core expertise of not just clinical development but also technology. Something that IQA possesses.

Data Engineering content

Our DCT Services

Telemedicine

With IQA’s remote monitoring solution, you can reduce site visits significantly by facilitating easy and accurate means of enforcing trial protocols without deviations.

  • Increase patient recruitment
  • Reduce operations burden
  • Control clinical development costs
Telemedicine

Wearables

Health Devices & Wearables

Leverage the meteoric rise of wearables and health-tech gear to enhance your clinical trials with our solution that can assist in implementing wearables technology in a non-intrusive way.

  • Gain higher quality results
  • Significantly high volumes of data
  • Easy setup and operational process

Remote Monitoring

IQA’s Remote Monitoring solution can help you avoid the complexity of tracking, monitoring and analyzing data when conducting clinical studies at diverse sites or at patients’ home.

  • Access to diverse datasets
  • Eliminate geographical barriers 
  • Low budget clinical research
Remote Monitoring

Remote eConsent

eConsent

Ensure compliance while enhancing patient experience and recruitment rate by securing e-signatures from patients or subjects after they review study documents remotely.

  • Better patient enrollment for studies
  • Get real-time insights of patient recruitment
  • Reduce participant drop-out via engagement

eCOA & ePRO

With IQA’s platform you can fetch clinical outcomes assessments (COAs) and patient reported outcome (PRO) digitally ensuring seamless, consistent and faster data collection.

  • Reduces hassle of transportation for patients
  • Faster and consistent data collection
  • Greater patient safety and access to real world data
eCOA & ePRO

Build high-functioning infrastructure and data transformation engine taking advantage of our experienced team of data engineers and consultants. We can modernize and optimize your data ecosystem to create a resilient growth formula for your business.

DCT is the way to be relevant during disruptions

Decentralized clinical trials is likely the natural evolutionary step in the way clinical development impact life sciences and life in general.

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