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    Clinical Outcome Assessments

    What are Clinical Outcome Assessments (COAs)? What do they measure?

    Learn more about COAs
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    700+ exclusive COA distributions on behalf of their copyright owners

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    PROQOLID™: the largest COA database

    7,000+ COAs described in details and accessible in this unique database

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    Mapi Research Trust provides turnkey solutions for your Clinical Outcome Assessments (COAs) strategies - including COA databases, targeted literature reviews, licensing.

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    Online access to all our services and COA databases

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    What are eBooklets?

    Find out more about this step-by-step guidance for valid digitization of COAs

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    Author Collaboration

    Our team is dedicated to assisting authors in the daily management of their questionnaires and all derivatives, including translations and electronic versions

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    New whitepaper

    Digitizing COAs: A streamlined approach to approval

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    New whitepaper

    COAs and copyright: How to mitigate risks of infringement and misuse in clinical research and practice

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    About us

    Mapi Research Trust is a non-profit organization dedicated to improving patients’ quality of life by facilitating access to Clinical Outcome Assessments(COAs).

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    A global team of multi-disciplinary experts

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    Collecting & Processing Patient Centered Outcomes information for more than two decades

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  4. Health Technology Assessment

Health Technology Assessment

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Articles

  • 2018. Gannedahl M et al. – Initiatives driving accelerated access to medicines in Europe: Review of recent concepts and developments
  • 2017. Udechiku A et al. – The Value of Health Technology Assessment Scientific Advice
  • 2013. Medic G – Conditional reimbursement of drugs in the Netherlands
  • 2010. Yi Y et al – Economic models in type 2 diabetes

Posters & Presentations

  • 2017. ISPOR European Congress – Processes and requirements for health economic assessment of antibiotics for HTA purposes: Time for a paradigm shift?
  • 2017. ISPOR European Congress – Comparison of early scientific advice processes in UK, France, and Germany (HTA only): Tips and tricks
  • 2017. ISPOR European Congress – Comparison of recent HTA appraisals of orphan drugs by NICE, SMC, and HAS in 2015- 2017
  • 2017. Forúm Assistência Farmacêutica e Farmaco-economia – Innovative Pricing Models
  • 2017. HTAi – Early HTA dialogue: Trends and evolution toward integrated advice
  • 2017. AMCP Managed Care Specialty Pharmacy Annual Meeting – Early Integrated Scientific Advice as a tactic to support successful regulatory approval, reimbursement and patient access
  • 2016. ISPOR European Congress – From Testimonials to Qualitative Research Embedded in Clinical Trials: How do HTA Bodies Consider the Voice of Rare Disease Patients When Granting Access to Orphan Drugs?
  • 2015. ISPOR European Congress – From Phase II Studies to HTA Submissions: Optimal Use of Evidence for Informed Decisions
  • 2015. ISPOR European Congress – Are Vaccines Getting a Fair Deal? Health Technology Assessment of Vaccines Across Europe
  • 2015. ISPOR European Congress – Regional Versus Centralized HTA: Implications for the Assessment of Cancer Drugs
  • 2014. ISPOR European Congress – An Examination of the Regulatory and Reimbursement Processes for Biobetters and Comparison with Biosimilars
  • 2014. ISPOR European Congress – An analysis of the health technology assessment recommendation and guidance on use of EQ-5D-5L in cost-effectiveness modeling
  • 2014. ISPOR International Annual Meeting – How are Biosimilar Medicines Appraised as Health Technologies? An Evaluation of Appraisal Processes in Mulitple Countries
  • 2013. ISPOR European Congress – Pricing and Reimbursement Analysis of Lifestyle Medicines in Serbia
  • 2013. ISPOR Europan Congress – Impact of Pharmacoeconomics Modelling on Reimbursement of Medicines in Serbia
  • 2013. ISPOR European Congress – What are the Key Drivers of Reimbursement for Biosimilars? An Explanation of Reimbursement Process and Recommendations across Nine Countries
  • 2012. ISPOR European Congress – Value and the Multiple Criteria Used in OECD Countries’ Medicine Reimbursement Decision-Making Processes Using Health Economic Evidence
  • 2011. ISPOR European Congress – The Impact of Regulatory (FDA and EMA) and EUNETHTA Guidelines on Patient-Reported Outcomes and Health-Related Quality of Life on Market Authorisation and Pricing
  • 2010. ISPOR European Congress – Perception of Pharmaco-Epidemiological Studies by Physicians and Motivation to Participate: French Situation
  • 2009. ISPOR European Congress – The Use of Survival Analyses for Cost-Effectiveness Models: An Evaluation of Methods Used in NICE Appraisals
  • 2009. ISPOR European Congress – Market Access in Germany: Where Next?
  • 2008. ISPOR European Congress – The Significance of Patient-Reported Outcomes to Facilitate Market Access During a Product Lifecycle
  • 2008. ISPOR European Congress – Fast is Best! Is Rapid Health Technology Assessment to Support Market Access Decision-Making a Good Thing?
  • 2008. ISPOR European Congress – Health Technology Assessment Research in Europe: Gathering the Data
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