MedTech & Pharma
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.
Certifications
OUR CAPABILITIES
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Clinical Database Programming
Empower your clinical research with our certified experts in industry-leading EDC systems, ensuring the best-fit system captures all study data needs and delivers high-quality programming through scalable, cost-effective global resources.
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Clinical Data ManagementYou 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.
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Biostatistics and Statistical Programming
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.
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Medical Writing and Regulatory Publishing
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.
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Pharmacovigilance
Our experienced team will create a safety management plan and provide the support you need using our robust safety system.
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Centralized Monitoring
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.
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Data Visualization
We perform expert data analysis for clinical reports and deliver medical data visualizations that identify problems and mitigate risks.
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Functional Service Provider Resourcing
Boost your productivity, improve quality, and increase speed with our flexible teams, and scalable Functional Service Provider model.
Our Partners
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
Need an expert opinion?
Contact one of our experts to accelerate your innovation today.