ClinVigilant

Technology/Service ProviderPrivate Company
Dartford, United Kingdom
WebsiteLinkedIn
2017
Founded
10-50
Employees

About ClinVigilant

Clinvigilant is a global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, eCRF, eConsent, eTMF, eSource, CTMS, IWRS, ePRO, and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials . Enquiries > [email protected]

Services

Electronic Data Capture (EDC)Trial Master File (TMF, eTMF)Digital Technologies for Patient EngagementeSourceDecentralized and Hybrid Trials, DCTseConsentePROBiostatistics, Trial Support SoftwareClinical Trial Management Systems (CTMS)eClinical Cloud

Therapeutic areas

OncologyDermatologyInfectious DiseasesPsychiatryRespiratoryHematologyDigital HealthCardiologyNephrologyOphthalmology

Experience & capabilities

Trial phases:Phase 1Phase 2Phase 3Phase 4
Products:Medical DevicesTherapeutic productsVaccines
Trial geography:EuropeGlobalAfricaCentral AmericaEast AsiaMiddle EastNorth AmericaUnited States of AmericaUnited Kingdom
Languages:EnglishSpanish
Compliance:Audited by FDAGDPR compliant21 CFR Part 11 compliantHIPAA ICH-GCP GDPR and 21 CFR Part 11 compliant

Team

  • Mili PatelGlobal Business Development ManagerLinkedIn
  • Parthesh RavalDirector of MarketingLinkedIn
  • Miguel LopezDirector of Business DevelopmentLinkedIn

Browse companies by location

Dartford, United KingdomUnited Kingdom

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