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palanskiP

Konstantine Palanski

@palanski
Toronto 3.0
PAAB Notice
The responses, guidance, and advisories provided by the Pharmaceutical Advertising Advisory Board (PAAB), including but not limited to those available through the PAAB Forum, the PAAB website, and any PAAB correspondences, are specifically intended to assist individuals navigating the PAAB preclearance system. Repurposing or reproducing this content without written consent from the PAAB Commissioner is strictly prohibited. This prohibition includes, but is not limited to, use in machine learning or AI models.
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Recent Best Controversial

  • NEW Renewals Management Dashboard
    palanskiP palanski

    @danthony

    I kid you not, I was just saying the other day to our team how this would be a really great thing to have (and dreaming about it for much, much longer). Thanks so much for this excellent upgrade!

    Guidance on Submission Procedures

  • Emails to HCPs regarding conditional reimbursement recommendations
    palanskiP palanski

    @cl This might be helpful: https://forum.paab.ca/topic/2048/email-update-on-cadth-recommendation?_=1620393473878

    FYI post-approval change/preclearance exemption/what requires review/PAAB scope

  • Disclosure requirements of competitor names/schedules
    palanskiP palanski

    Hi PAAB—could you kindly clarify if the below section of the code applies solely to the manufacturer's product or all products mentioned within an APS? Does this vary if the manufacturer opts to include the brand name of another manufacturer's product within an APS, not just its generic name (assume this is permissible due to an acceptable head-to-head trial)?

    2.2 In all APS for pharmaceutical products, the brand or trade name, the non-proprietary or generic name and the Federal drug schedule of the product must appear in juxtaposition at least once within advertising copy and must be in good contrast and be legible.
    
    PAAB Code

  • Draft Guidance on Burden of Disease Presentations
    palanskiP palanski

    @jennifer-carroll This is an exciting change! I'm sure we're all wondering why the PAAB is evolving its stance on this subject, which has in the past generally been a no-go zone. Could you provide any context?

    Announcements external guidance document draft disease info

  • Formulary pieces
    palanskiP palanski

    @mef It definitely would not be.

    FYI post-approval change/preclearance exemption/what requires review/PAAB scope

  • Consumer landing page disclaimer on HCP-facing materials
    palanskiP palanski

    Hi there! I understand there is new a requirement to include a disclaimer when linking to websites that have a consumer-facing landing page from HCP materials (e.g., micetype linked to the site URL that states "The website landing page of drugx.ca is open to the general public." or similar).

    Could you help clarify what precipitated this requirement and concern it addresses? Additionally, do URLs that direct HCPs to HCP-only landing pages/content require similar disclaimers?

    Claims & Support/References for Claims

  • Gating requirements for HCP journal
    palanskiP palanski

    Hi @mimic909!

    If it's properly gated for HCPs, then yes. You might also find this PAAB forum response helpful as well.

    Electronic Media
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