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So FYI for anyone who isn’t familiar with pharma approvals…...

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    So FYI for anyone who isn’t familiar with pharma approvals… globally the regulatory body will post its approvals as part of the meeting minutes on their site.

    here is the link to the PDCO for ema… ie the guys approving ATL…
    https://www.ema.europa.eu/en/committees/pdco/pdco-agendas-minutes-meeting-reports

    I used to work for a pharma company locally and would keep an alert for whenever the TGA would publish monthly meeting approvals/rejections. Would also mean I’d find out about competitor label extensions before HQ would advise the rest of our field force.

 
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