InVentiv Health Clinical

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inVentiv Health is a global professional services organization designed to help the biopharmaceutical industry accelerate the delivery of much-needed therapies to market. Our combined Clinical Research Organization (CRO) and Contract Commercial Organization (CCO) offer a differentiated suite of services, processes and integrated solutions that improve client performance.[1]

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inVentiv Health Commercial
Type Private
Industry Pharmaceuticals
Founded 1999
Headquarters Boston, MA
Number of employees 10,001+ employees


inVentiv Health Clinical was launched in January 2013 as the clinical segment of inVentiv Health, a best-in-class team of global healthcare experts offering clinical, commercial and consulting services designed to provide a comprehensive customer experience that delivers greater long term value.

With roots dating back to 1984, inVentiv Health Clinical is an amalgamation of a number of clinical services companies who, when brought together, had the skills and experience to allow inVentiv Health Clinical to become a leading global Clinical Research Organization.


  • Phase I-IIa
  • Bioanalytical
  • Phase IIb-III
  • Late Stage
  • Quality Assurance
  • Consulting
  • Functional Services
  • Clinical Staffing



inVentiv Health Clinical's Safety and Pharmacovigilance team supports clinical trials and post-marketing safety surveillance. Working globally, inVentiv Health Clinical can provide integrated or stand-alone services to support product safety monitoring in compliance with regulatory requirements for safety surveillance in pre- and post-approval settings. inVentiv Health Clinical has the flexibility and experience to deliver, whether our clients’ needs are best met on a project-by-project basis, through a functional service provider or consultative relationship. Currently, we have 32 active partnerships with clients; seven of them focused specifically on pharmacovigilance. Our global, integrated team of skilled professionals has deep expertise in direct patient care and industry-specific pharmacovigilance services are highly experienced in drug safety, pharmacovigilance, and pharmacoepidemiology and understand the changing regulatory environment. We have the capability to submit expedited and aggregate reports globally. Our staff can handle all varieties of global submissions and submit them electronically or via fax, courier or hand delivery, as is required in Argentina.


To manage clinical-trial safety, the team provides qualified medical analysis and review of all Serious Adverse Events (SAEs), and creates the necessary 21 CFR Part 11-compliant materials for submission to US and international regulatory authorities and data safety monitoring boards (DSMBs). Services include:

  • SAE’s monitoring
  • Expedited SAE reports
  • SAE safety narratives
  • Annual safety reports
  • Safety databases
  • Interim safety listings
  • Risk management strategies.


With regulatory authorities placing an increased emphasis on risk assessment for marketed drugs, companies can no longer rely solely on periodic reports that list adverse events (AEs). Regulatory authorities today expect greater assessment and analysis of AEs, as well as recommendations for increased safety surveillance monitoring to achieve earlier signal detection. To assist companies during post-marketing surveillance, the Global Safety and Pharmacovigilance team:

  • Creates customized programs for managing spontaneous AE reporting
  • Provides uninterrupted (24/7) coverage by qualified personnel
  • Transfers data electronically in compliance with ICH E2B (M2)
  • Provides medical information services for literature review to detect signals and/or identify trends
  • Prepares periodic safety update reports (PSURs)
  • Assists in liability claims, causality assessments, and medical evaluations
  • Reviews and assesses in-house safety data
  • Reviews labeling modifications (SmPC variations) for consistency with safety data
  • Writes standard operating procedures and working practices related to organization, infrastructure, and workflow for pharmacovigilance activities
  • Prepares and reviews risk/crisis management strategies
  • Analyzes epidemiologic data to determine strategies for signal detection in safety-surveillance studies and to establish registries for continuous safety monitoring
  • Conducts workshops and courses on pharmacovigilance requirements
  • Designs, reviews, and implements risk-management plans and safety surveillance studies to include cohort, case-control, post-marketing surveys (simplified Phase IV), registries, and database studies.



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