IMT Feedback

    Did the IMT help you in finding the resource you needed?

    Your feedback helps us improve the toolkit in the future.

    Are you experiencing difficulties? Please include information on your search query and used browser



    Input this code: captcha

    Skip to content
    • Homepage
    • Browse Resources
    • Questions
    • Use Cases
    • Collections
      • Clinical Trials Toolkit
      • Orphan Drug Guide
      • Mentoring packages
      • EJPRD online courses
      • Advisory Committee for Therapeutics Toolkit
    • Services
    • My IMT
    EJPRD IMT

    Accelerated assessment

    Categories

    • Translational Project Management
      • Project Management
        • Clinical Trial Management
        • Data Management
        • Project Management Manual
      • TPP
      • Reverse Planning Approach
      • Technology Transfer Offices (TTO's)
        • What is technology transfer?
        • TTO and Intellectual Property Management
        • TTO and Commercialisation
      • Consulting & Advice
        • TREAT-NMD Advisory Committee for Therapeutics (TACT)
    • Research and Drug Development
      • Disease Model
        • In Silico Model
        • Cell Model
        • Animal Model
      • Disease or Translational Resources
        • Patients Registries
        • Natural History
        • Patients Information
        • Target Patient Value Profile
        • Data Bases or Tools
        • Networks
        • Biobanks
        • Biomarkers
      • Drug Discovery
        • Small Molecules
        • Advanced Therapies
        • Target Validation
        • High Throughput Screening (HTS)
        • Bioassays
        • Drug Repurposing
      • Data Collection
        • Patient Registries
      • Clinical Development
        • Safety Reporting
        • Dissemination
        • Clinical Trial Design
        • Endpoints
        • Patients
    • Regulatory Science
      • Preclinical Studies
        • Animal Model
        • Safety
        • Efficacy
      • Early Acces Support
        • Orphan Drug Designation
        • Orphan Drug or Medical Device Designation
        • Scientific Advice
        • SME Office
        • Patient Advice
        • Orphan Medicines
        • Nan-byo Designation
        • Paediatric Medicines
        • Advanced Therapy
      • Biological
      • Clinical Development
        • Good Clinical Practices
        • Compassionate Use
      • Marketing Authorisation
        • Marketing Authorisation Road Map
        • Advanced Therapy procedure
        • Conditional Approval
        • Exceptional Circumstances
        • Accelerated Assessment
        • FDA Priority Review Voucher
      • Ethic and Legal Issues
        • Data protection and confidentiality
        • Clinical Studies
        • Clinical Trials
        • Genetics
        • Paediatrics
        • Biomarkers
        • Animal Welfare
      • HTA
        • National HTA Bodies
        • European HTA Bodies
        • International HTA Bodies
    • Funding Sources
      • Public Funding Sources
        • Awards
        • Fellowships
        • Accelerators or Incubators
        • Grant
      • Private Funding Sources
        • Crowdfunding
        • Venture Capital or Angel Investment
        • Foundations
        • Awards
        • Fellowships
        • Accelerators or Incubators
        • Grant
        • Loans
    • Uncategorized
    • Intellectual Property
      • Basics of Intellectual Property
        • Types of Intellectual Property
        • Intellectual Property Teaching Kit
        • European IP Helpdesk
        • Freedom to Operate (FTO)
      • Patent Filing
        • International Patent Cooperation Treaty (PCT) Route
        • European Route
        • American Route
      • Patent Search
        • Patentscope
        • Espacenet
      • Market Exclusivity
        • Incentives in Orphan Medicines
        • Incentives in Paediatric Medicines
      • Commercialisation

    Subjects

    All SubjectsClinical Trials ToolkitRegulatory AffairsResearch and Drug DevelopmentEarly Access SupportPreclinical ResearchClinical ResearchBasic ResearchIndustrial Development or SMEPrivateClinical DevelopmentScientific AdviceClinical TrialsGrantOrphan DrugPublicRare DiseaseClinical Trial DesignGuidelineIn silicoRegulatory Advice

    Regions

    • All regions
      • International
      • Europe
      • USA
      • Asia

    Accelerated assessment

    Published by IRDiRC

    Regulatory AffairsMarketing AuthorisationCentralised ProcedureAccelerated Assessment

    The accelerated assessment allows a faster assessment process for the marketing authorization application under the Centralised Procedure

    View this resource Bookmark this resource

    The toolbox has been developed through funding from the EJP RD project.

    The European Joint Programme on Rare Diseases is an initiative that has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement N°825575

    © 2023 EJPRD IMT | GetYos IT
    IMT Cookie Overview
    The EJPRD IMT uses cookies to help you save articles for future use and to improve the website. By clicking “Accept All”, you consent to the use of ALL the cookies. However, you may visit "Cookie Settings" to provide a controlled consent.

    Please also read this disclaimer carefully before using the EJPRD IMT
    Accept AllCookie SettingsRead More
    Manage consent

    Privacy Overview

    This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may affect your browsing experience. See our Cookie Policy
    Necessary
    Always Enabled
    Necessary cookies are absolutely essential for the website to function properly. These cookies ensure basic functionalities and security features of the website, anonymously.
    CookieDurationDescription
    Bookmark Cookie12 monthsThis cookie saves your bookmarked resources to your local browser for future use.
    Cookie Policy11 monthsThe cookie is set by the GDPR Cookie Consent plugin and is used to store whether or not user has consented to the use of cookies. It does not store any personal data.
    Analytics
    Analytical cookies are used to understand how visitors interact with the website. These cookies help provide information on metrics the number of visitors, bounce rate, traffic source, etc.
    SAVE & ACCEPT
    Powered by CookieYes Logo