Cross-domains agenda

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    27 June '22

    Webinar: Healixia essentials: what you should know about the RIP (Responsible person for Information and Publicity)

    Online

    The how, the why and the who: all you would like to know about the RIP (Responsible for Information and Publicity) when working outside regulatory affairs. This webinar is aimed at life science professionals who are not necessarily familiar with the term or who would like to learn more on it.

    Healixia Essentials: during several short sessions throughout the year, we tackle different terms, concepts or processes to keep all professionals up to speed with the essentials of the life sciences industry.

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    13 September '22

    Webinar: The sources of life sciences regulations - part I: Medical devices

    Online

    This first session on the “Sources of life sciences regulation” is intended to provide an overview of the main body of the legislation applicable to the placing on the market or making available of medical devices in the European Union. The session will include a specific part on the Belgian legislation. It will also provide the audience with practical tips on researching applicable laws.

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    18 October '22

    Webinar: The sources of life sciences regulations - part II: Medicinal products

    Online

    This session is the second part of a two-part training course on the “Sources of life sciences regulation”. It serves to provide participants with a high-level overview of the rules and regulations applicable to medicinal products for human use in the European Union. The session will include a specific part on the Belgian legislation. It will also provide the audience with practical tips on researching applicable laws.

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    27 October '22

    Healixia Essentials: the role of the MSL (Medical Science Liaison)

    Online

    SAVE THE DATE.

    More information will follow soon.