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Webinars related to Post-Approval Maintenance

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eCTD in Australia: key steps to start a successful submission

28th June 2022

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Software Medical Devices – Considerations for Regulatory Compliance Success

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How technology optimizes the publishing process for regulatory submissions

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Global framework of interactions with Heath Care Professionals : Loi anti-cadeaux in France

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Basic rules of pharmaceutical advertising in France

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US NDA versus EU MAA eCTDs – Exploiting the Synergies and Mastering the Differences

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What you need to know to submit Study Data to FDA & what the new FDA Technical Rejection Criteria means for you

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Webinar

Central American Regulation for Drug Products (LATAM)

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An Update to In Vitro Diagnostics Regulatory Requirements Worldwide

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Biotech Drug Development Challenges and Case Studies (CMC)

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eCTD in China

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Electronic Submission in the EAEU – the challenges

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Optimal Patient Access
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Optimal Patient Access
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