PHARMA & MEDTECH

CLINICAL DATA SERVICES

Data-Driven Insights for Better Business Decisions

We employ best-in-class clinical trial data and analytics services through teams that are flexible, scalable, and responsive to varying clients and scopes.

What We Offer

Our service capabilities range from statistical programming and biostatistics, clinical data management, risk-based monitoring, and data visualization to medical writing/publishing, and pharmacovigilance, all of which help you build a robust Electronic Case Report Form (eCRF) and better understand.

View trends, risks, and track performance with our data visualization tools, better understand adverse events through rigorous pharmacovigilance, and submit thorough, accurate reports to regulatory agencies with the help of our medical writing team.

Our range of services delivers the quality, expertise, and speed you need to advance your study with confidence. Get collaborative, affordable support for clinical data management, biostatistics and programming, RBM, medical writing, and pharmacovigilance groups — whether you need minimal support or a dedicated groups.

OUR CAPABILITIES

Statistical Programming & Biostatistics
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Our skilled statisticians and programmers have experience working on innovative designs in complex, therapeutic areas. If your study design demands a highly experienced medical device biostatistics partner, Veranex is the right choice for you.

Clinical Data Management
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You can rely on Veranex for expert data management that is compliant and accurate regardless of trial type. We use our 21 CFR Part 11-compliant processes to support your success.

Risk Based & Central Monitoring (RBM)
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We offer expert medical device remote monitoring, critical data insights, and web analytics training support so you can optimize on-site monitoring and efficiently identify risks.

Data Visualization
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We perform expert data analysis for clinical reports and deliver medical data visualizations that identify problems and mitigate risks.

Medical Writing & Publishing
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Our in-house experts will partner with you to deliver documents that are 100% compliant with FDA, EMA, and other regulatory bodies. From clinical protocol support to conference posters, you can expect the highest caliber of medical documentation and regulatory publishing services.

Pharmacovigilance & Postmarket Surveillance
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Our experienced team will create a safety management plan and provide the support you need using our robust safety system.

Functional Outsourcing / Full-Service Resourcing
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Boost your productivity, improve quality, and increase speed with our flexible teams, and scalable Functional Service Provider model.

CDS

OUR LOCATIONS

Europe

Kyiv, Ukraine
172, Antonovicha Street
Suite 515
Kyiv UA-30
Ukraine

Kharkiv, Ukraine
42A Tobolskaya St.
Ste 504
Kharkiv Kharkivska oblast UA-63
Ukraine

Asia Pacific

Kolkata, India
Ecospace Tech Park,
Building 4A, 2nd Floor,
Newtown Action area-II,
Rajarhat, Kolkata – 700156
India

Bangalore, India
No.23 & 24, 2nd floor,
AMR Tech Park 1A, Hongasandra,
Hosur Main Road,
Bangalore, Karnataka – 560 068
India

LEARN ABOUT

OUR OTHER SERVICES

Preclinical Services

Global Clinical Research

Product Design & Engineering

Regulatory Affairs & Quality Management

Commercial Strategy & Market Access

Clinical Data Services