Interactive Voice/Web Response System (IVRS/IWRS)

At ClinovaPack, we offer cutting-edge Interactive Voice/Web Response System (IVRS/IWRS) solutions to streamline your clinical trials. Our IVRS/IWRS is the backbone of your trial management, ensuring efficiency, compliance, and seamless communication throughout the trial process.

Main Set up at Our Strategic Business Partner in the UK

At ClinovaPack, we recognize the critical importance of a robust infrastructure and expertise in supporting the intricate processes of clinical trials. That’s why we’ve forged a strategic partnership with industry-leading experts based in the United Kingdom. Our partnership ensures that your IVRS/IWRS operates from a secure and reliable location, backed by state-of-the-art facilities and seasoned professionals with years of experience in clinical trial support.

Infrastructure Excellence: Our UK-based partner boasts state-of-the-art infrastructure tailored specifically for the demands of clinical trial management. From cutting-edge data centers to redundant systems, we ensure the highest standards of reliability and security for your trial data.

Regulatory Compliance: With ever-evolving regulatory requirements, compliance is non-negotiable. Our partner’s in-depth understanding of UK and international regulations, including EU GDPR and FDA guidelines, ensures that your trial operates within the bounds of regulatory compliance at all times.

Expertise and Experience: Benefit from the wealth of experience and expertise that our UK partner brings to the table. Their team of seasoned professionals, including IT specialists, regulatory experts, and project managers, is dedicated to providing unparalleled support throughout every phase of your clinical trial.

Proximity to Research Hubs: Located in the heart of the UK, our partner is strategically positioned to tap into the vibrant research ecosystem of the region. With proximity to renowned research institutions, academic centers, and medical facilities, we facilitate seamless collaboration and access to diverse patient populations for your trials.

Site Initiation Management

Kickstart your trial journey seamlessly with ClinovaPack’s comprehensive site initiation management tools. Whether through phone or web interfaces, our system simplifies the setup of new trial sites, expediting the commencement of critical clinical activities.

Patient Enrollment

Harness the power of streamlined patient enrollment with ClinovaPack. Our system facilitates a seamless enrollment process, ensuring adherence to protocol requirements while optimizing the management of study cohorts.

Drug Management

From meticulous inventory tracking to automated replenishment of investigational products, ClinovaPack revolutionizes drug management. Say goodbye to stockouts and supply shortages, as our system ensures continuous availability of study medications with pinpoint accuracy.

Patient Enrollment

Effortlessly recruit participants with our streamlined enrollment process. Ensure accuracy and compliance with integrated data collection and verification. Seamlessly integrate with patient databases and study protocols for efficient enrollment procedures.

Randomization

Eliminate bias with automated randomization algorithms. Customize schedules to fit your study design’s unique needs. Enhance transparency and data integrity with real-time tracking of randomization outcomes.

Why Choose ClinovaPack?

21CFR Part 11 Compliance

Our unwavering commitment to regulatory compliance ensures that ClinovaPack aligns seamlessly with the stringent requirements of 21CFR Part 11. This compliance guarantees the integrity, security, and authenticity of your trial data at every step.

User-Friendly Interface

ClinovaPack boasts an intuitively designed interface crafted with end-users in mind. Navigating through complex trial processes becomes a breeze, empowering site personnel to harness the full potential of the system with minimal training.

Direct Data Entry

Eliminate the hassle of manual data entry errors with ClinovaPack’s seamless integration capabilities. By enabling direct data entry from the source, we mitigate the risk of transcription errors, ensuring pristine data integrity throughout your trial.

Client Testimonials

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