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THE IVDR TOP 8 – A Roadmap For Transitioning To The European in vitro Diagnostic Medical Devices Regulation (IVDR)

  • Whitepapers

    THE IVDR TOP 8 – A Roadmap For Transitioning To The European in vitro Diagnostic Medical Devices Regulation (IVDR)

    THE TIME FOR ACTION IS NOW. GET YOUR ROADMAP FOR IVDR COMPLIANCE. Notified Body (NB)...

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  • Whitepapers

    The Value of PMO in Life Sciences

    PMI research reveals that 90% of executives say the execution of strategic initiatives are the key...

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  • Whitepapers

    Outsourcing in Life Sciences: A Pivot To Strategic Relationships

    Outsourcing in the life sciences continues to transform from a transactional sales relationship to...

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  • Whitepapers

    Guide to a Successful Drug Development Technology Transfer

    During a drug development technology transfer, the focus is on moving products from one...

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  • Whitepapers

    U.S. Prescribing Information (USPI) & the Impact of Pediatric and Geriatric Guidance on Labeling

    The final rule, Requirements on Content and Format of Labeling for Human Prescription Drug and...

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  • Whitepapers

    Achieve Compliance: Converting U.S. Prescribing Information (USPI) Labels

    The new Pregnancy Lactation Labeling Rule (PLLR) in the U.S. Prescribing Information (USPI) was...

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