VISITOR Clinical Study Demonstrates Feasibility and Utility of Transparency Life Sciences’ New Virtual Trials Platform

Kick off the Trial Faster and Fulfill the Emerging Regulatory Requirements

TLS’s TPC proprietary platform is a cost-effective means of producing an optimized protocol.

One protocol to develop or many within a portfolio of assets, TPC™ is the premier proprietary technology that facilitates the collection and analysis of qualified stakeholder (patients, caregivers, clinicians) feedback. Their input provides fit-for–purpose clinical outcome assessments for the purposes of regulatory decision making.

TLS’s TPC proprietary platform arms you with the competitive tools you need:

  • Cost: Provides a cost-effective means of producing an optimized protocol while fulfilling the emerging regulatory requirements and minimizing amendments.
  • Time to Market: Can decrease the overall study timelines. Improve study execution timelines and budget. >
  • Qualified Patients: Testing study feasibility through interacting with qualified individuals (patients, caregivers) and identifying what matters most to them and what ways they can participate.
  • Qualified Clinicians: Interacting with experienced clinicians outside of the study team to gain additional input on key aspects of the proposed study design.
  • Analytics: Our analytics team analyzes the data from these two key groups and provides sponsors with actionable information that can provide valuable input to the protocol design of a study.
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Patient Input and Researcher Feedback Produce a Protocol that Can Enroll Quickly and Minimize Amendments

DESIGN

Our fit-for-purpose proprietary system empowers you to collect key impacts and concepts from qualified stakeholders. This is critical to informing the protocol endpoints that will be considered significantly robust for regulatory decision-making.

VERIFICATION

Our system can also be used to help validate the protocol design before execution. The system engages qualified stakeholders whose real-world experience can validate the protocol and enhance patient recruitment and retention.

FEASIBILITY

Our system ensures the feasibility of requirements for patient eligibility, site visits, and procedures. Qualified stakeholder feedback on protocol design enables sponsors to minimize the potential for extra expense and delay caused by protocol amendments and resubmissions.

RESCUE

Our system connects sponsors and researchers with patients and clinicians who can help amend trial protocols that may need a helping hand. This input can assure qualified stakeholders are willing and able to meet protocol requirements and aligns endpoints with their needs.

Patient Input and Researcher Feedback Produce a Protocol that Can Enroll Quickly and Minimize Amendments

DESIGN

Our fit-for-purpose proprietary system empowers you to collect key impacts and concepts from qualified stakeholders. This is critical to informing the protocol endpoints that will be considered significantly robust for regulatory decision-making.

VERIFICATION

Our system can also be used to help validate the protocol design before execution. The system engages qualified stakeholders whose real-world experience can validate the protocol and enhance patient recruitment and retention.

FEASIBILITY

Our system ensures the feasibility of requirements for patient eligibility, site visits, and procedures. Qualified stakeholder feedback on protocol design enables sponsors to minimize the potential for extra expense and delay caused by protocol amendments and resubmissions.

RESCUE

Our system connects sponsors and researchers with patients and clinicians who can help amend trial protocols that may need a helping hand. This input can assure qualified stakeholders are willing and able to meet protocol requirements and aligns endpoints with their needs.

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