The safety requirements for medicinal products are high. Swiss laws and regulations are constantly being adapted. Patients, specialists and authorities demand more and more information. Adverse effects must be reported to Swissmedic. We would be happy to advise you.

Frequently required services

  • Strategic consultation

    Strategic consultation

    Use our experience and know-how on a strategic level:

    • Evaluation and optimisation of existing pharmacovigilance systems for Swiss pharmaceutical companies
    • Development of new pharmacovigilance systems including contracts and documentation
    • Providing the function of Responsible Person PV in Switzerland
  • Operational support

    Operational support

    We would be delighted to support you with your daily business:

    • Receiving and processing ADR notifications from Switzerland
    • Carrying out regular literature searches for Switzerland
    • Review and submission of PSURs/PBRERs and RMPs

Your contact

Any questions?
I would be delighted to answer them.

Katharina Oehler
Scientific and Managing Director
T +41 44 787 70 20
Send email


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Keeping track of things? Our visual representation of all pharmaceutical processes helps:
Swissmedic offers further information on pharmacovigilance:
We have been committed to serving our clients enthusiastically and cooperatively since 1997: