Skip to main content
  • Ministries
  • E-Citizen
    • EN
      • EN
      • LT
    /en/State Medicines Control Agency of Lithuania
    Menu
    Structure and contacts
    • About us
    • Contact information
    • Contacts
    ServicesLegislationMarketing authorisation
    • Marketing authorization fees
    • E-submission
    • Authorisation procedures
    • LT RMS
    • Zero – Day procedure
    • Summary product characteristic, labelling, package leaflet
    • Variation procedures
    • Transfer of marketing authorisation holder
    • Parallel import
    • Common procedures
    • Areas of special competence
    • Scientific-regulatory advice
    National requirements in MRP/DCPBaltic package procedureHealth technology assessment
    • Information to the applicants
    • Information for healthcare specialists or patients organisations
    Clinical trialsPharmacovigilanceInternational CooperationLicensing of pharmaceutical activity
    • Licensing of Pharmaceutical Activity of Legal Entities (enterprises)
    • Licensing of activity related to narcotic and psychotropic substances of Schedule II and III, or psychotropic substances of Schedule III
    • Sizes of state fees
    • Applications for obtaining a licence
    • Statistical data
    Supervision of manufacturing and distribution
    • Suspected quality defects in medical products
    • Good manufacturing practice
    • Good distribution practice
    • Rapid alerts
    Submission and examination of complaints concerning the activities of the AgencyQuality and information security policyAssessment of the quality of services provided to persons/customersImportant information
    • International cooperation
    • Report of baches and quantities of the medicinal product
    • Medicines consumption (2022)
    • Requirements applied for writing of prescriptions of other EU countries and dispensing of medicinal products
    • Brexit
    News
    • Assessment of the quality of services

    News

    • 24-02-2025

      Regarding medicinal products for which „sunset clause“ may already be applied

    • 20-12-2024

      Important information about applications

    • 16-05-2024

      Attention Holders of Wholesale Distribution and Manufacturing Licenses

    More news

    Topical information

    • REGISTER OF MEDICINAL PRODUCTS
    • NATIONAL REQUIREMENTS IN MRP/DCP
    • BALTIC PACKAGE PROCEDURE
    • HOW TO FIND US

    Important Information

    • International Cooperation
    • Report of baches and quantities of the medicinal product
    • Medicines consumption (2022)
    • Requirements applied for writing of prescriptions of other EU countries and dispensing of medicinal products
    • Brexit

    Director

    Dovilė Marcinkė

    Dovilė Marcinkė

    Director

      • Curriculum vitae
      State Medicines Control Agency of Lithuania
        Legal entity code

        191351864

        Address

        Studentų g. 45A, Vilnius

        Email

        [email protected]

        Ph. no

        +370 5 263 9264

        Data about the institution are collected and stored in the Register of Legal Entities.
        • Cookie settings
        • Site tree