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We provide technical consulting and expertise across the product journey, helping our clients maximize the value of their available evidence and addressing gaps to support successful access and reimbursement strategies within their target markets.

Our team consists of technical experts including health economists, statisticians, medical writers, in-house graphic designers, commercial assessment analysts, systematic reviewers, and COA specialists, enabling us to provide bespoke, end-to-end solutions across the product lifecycle with the goal of optimizing market access.

 

Clinical outcomes assessment

Our experts can streamline your clinical development strategy with fit-for-purpose PROs and other COA instruments to support regulatory,  communication, and reimbursement strategies.​

Offerings include: ​

  • COA reviews (targeted literature reviews and gap analysis)​
  • COA development​
  • COA content validation​
  • COA interpretation
  • COA regulatory support
  • COA training​
  • Preference studies​
  • Utility studies​
  • COA general consultancy (e.g., clinical trial protocol reviews)​
  • COA publication/dissemination

Health economics

We design, construct, data populate, test and adapt economic models to demonstrate product value and increase likelihood of positive funding decisions in your target markets​.

Offerings include:​

  • Early analysis and economic modeling​ ​
  • Multi-country adaptation support​
  • Evidence generation strategy​
  • Post-launch economic tool development (e.g., iPad-based BIMs)​ ​
  • Consultancy and training (economic evidence generation strategy, mentorship of internal modeling teams)​
  • Clinical trial data analysis ​ ​
  • Real-world data analysis
  • Publications

Health technology assessment (HTA)

Clarivate can develop, coordinate and deliver a robust HTA strategy to effectively convey the benefit of your asset for favorable reimbursement outcomes in target markets​.

Offerings include: ​

  • HTA strategy development and support​ ​
  • HTA dossier development​ ​
  • HTA model and SLR development, critique and adaptation​ ​
  • Early HTA/scientific advice ​  ​
  • Customized submissions ​
  • Mock committee meetings ​​  ​ ​

Evidence generation

Clarivate can develop robust, reproducible, high quality systematic literature reviews and indirect treatment comparisons to support HTA submissions and Market Access activities. Our offerings include:

  • Systematic literature reviews
    • HTA submissions
    • Economic models​ ​
    • Product development ​
    • Market access strategy​  ​
  • Targeted literature reviews
    • Value message development
    • Core value dossiers​ ​
    • Global and local market access activities ​
    • Directing future research and evidence generation​
  • Statistical analyses
    • Feasibility assessments
    • Pair-wise meta-analysis​
    • Indirect treatment comparisons​
    • Network meta-analyses
    • Consultancy and training

Biopharma customer engagement solution

Uncover and truly understand customer perceptions, needs and behaviors so you can effectively engage with physicians, patients and payers.

Customer engagement
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Our latest thought leadership

Regulators and HTAs tune in to patient preference data Regulators and HTAs tune in to patient preference data
Blog June 26, 2023
Regulators and HTAs tune in to patient preference data

Obtaining the preferences of patients and their caregivers is not a new concept in healthcare. Increasingly, however, industry guidance documents utilize the term ‘patient preference’ in relation to new drug…

Let's get real about data and AI Let's get real about data and AI
Webinar
Let's get real about data and AI
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Drugs to Watch
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Blog March 29, 2024
Let's get real about data and AI

Joint Clinical Assessment (JCA) provides an opportunity for manufacturers and Health Technology Assessment (HTA) bodies to work more closely with one another; but what do these opportunities look like? And…

Companies to Watch 2023 Companies to Watch 2023
Companies to Watch 2023

Seven promising early-stage companies working on AI and ML applications for drug discovery and development

Bringing the patient voice into clinical trials with clinical outcome assessments Bringing the patient voice into clinical trials with clinical outcome assessments
Blog November 10, 2022
Bringing the patient voice into clinical trials with clinical outcome assessments

Clinical outcome assessments can take years to generate but may pay big dividends in patient-focused drug development, centering the patient experience and potentially bolstering a product’s case with regulators and…

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Learn how Clarivate consultants can provide the insight and foresight across your drug and device lifecycle.