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Quanticate Launches Updated Remote Source Data Verification (RSDV) Platform

Content Team by Content Team
8th September 2021
in News
Quanticate Launches Updated Remote Source Data Verification (RSDV) Platform

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Quanticate, a leading global data-focused clinical research organisation (CRO), has launched a new Remote Source Data Verification
(RSDV) Platform.

The 21 CFR part 11 compliant cloud-based application allows verification of multiple clinical research sites’ source data to be completed remotely by a specialist team at a centralized location.

Quanticate built the platform to help clinical trial sponsors reduce Clinical Research Associate (CRA) travel costs and time, negate the challenges
associated with movement restriction, increase data integrity and accelerate the detection of site issues, thus improving quality.

David Underwood, founding CEO and Chairman at Quanticate said “Quanticate is an experienced niche biometric CRO supporting businesses across the pharma and biotech sectors and we constantly explore ways to enhance the services we offer our customers.

“Throughout the COVID-19 pandemic, there have been significant challenges for clinical trial sponsors and sites alike resulting in renewed emphasis on creating remote approaches to improve efficiencies and adapt to travel restrictions.

“Our new Remote Source Data Verification (RSDV) platform will help to ensure that our customers operate more efficiently and safely while delivering clinical trial data with high integrity.”

As part of the Remote Source Data Verification (RSDV) service, Quanticate delivers centralized monitoring undertaken by a team with experience in the global conduct of clinical trials and extensive therapeutic, GCP and regulatory knowledge.

About Quanticate

Quanticate is one of the world’s largest global data-focused clinical research organizations (CROs) with a primary focus on clinical trial data, statistical analysis, and clinical trial reporting. As an expert in clinical data, Quanticate can rapidly provide high-quality teams that offer flexible solutions for clinical data management, biostatistics, statistical programming, pharmacokinetic/pharmacodynamic (PK/PD) analysis, medical writing, and statistical consultancy.

Quanticate meets the needs of drug and device development companies by offering customer focused resource solutions from fixed cost or functional service provider (FSP) models through to consultancy. Quanticate has become the trusted supplier of choice for many companies from niche biotechnology and device companies to top tier pharmaceutical giants.

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