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

    Form | 01-01-2017

  2. Braille declaration

    Form | 01-01-2017

  3. MEB Regulatory Science Day 2017

    Publication | 23-12-2016

  4. Classification overview legal status of supply NSAIDs

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

    Policy document | 24-11-2016

  5. 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

  6. 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

  7. 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

  8. Assessment report 2’-fucosyllactose, applicant Jennewein Biotechnologie GmbH

    A report on the initial assessment of 2’-fucosyllactose by the company Jennewein Biotechnologie GmbH.

    Report | 03-06-2016

  9. Heads of Medicines Agencies: Heads and IT directors meeting

    Publication | 01-06-2016

  10. HMA human stakeholders meeting

    Publication | 31-05-2016

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