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  1. Declaration Member State of origin parallel import

    Form | 01-01-2017

  2. Declaration for information intended for healthcare professionals of parallel imported products

    Form | 01-01-2017

  3. Application for parallel import marketing authorisation

    Form | 01-01-2017

  4. EMA: form for reporting a suspected adverse event of a veterinary medicinal product

    Form | 01-01-2017

  5. Braille declaration

    Form | 01-01-2017

  6. MEB Regulatory Science Day 2017

    Publication | 23-12-2016

  7. Classification overview legal status of supply NSAIDs

    The MEB has determined a classification system for OTC anti-inflammatories (NSAIDs).

    Policy document | 24-11-2016

  8. Assessment report DHA-rich algal oil, applicant NovoSana (Europe) B.V.

    A report on the assessment of DHA-rich algal oil by the company NovoSana (Europe) B.V. for substantial equivalence to DHA-rich ...

    Report | 02-11-2016

  9. Assessment report Chia seed, applicant DFInternational BV

    A report on the assessment of chia seed by the company DFInternational B.V. for substantial equivalence to chia seed, which has ...

    Report | 19-10-2016

  10. MEB 41: MEB policy concerning marketing authorisations without Dutch translations of the product information and/or mock-ups

    The MEB is aware of the fact that medicinal products are not always marketed immediately after authorisation. Following the ...

    Policy document | 18-10-2016