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  • Artificial Intelligence in the Health Care Industry: Part III

    Artificial Intelligence in the Health Care Industry: Part III

    In Part III of our series, Tony Ettwein, Managing Expert, Quality Center of Excellence, looks at the role AI can take within drug discovery, early safety signal detection, and diagnostics.

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  • EU MDR Preparation: Ensuring Compliance with Newly Adopted Regulations

    EU MDR Preparation: Ensuring Compliance with Newly Adopted Regulations

    The introduction of new EU MDR regulations brings updated requirements and challenges to device manufacturers. Read more from YourEncore Expert Judith Meritz on the future of EU MDR Regulations.

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  • Artificial Intelligence in the Health Care Industry: Part II

    Artificial Intelligence in the Health Care Industry: Part II

    In Part II of our series, Tony Ettwein, Managing Expert, Quality Center of Excellence, looks at the challenges and different opportunities for process integration of AI in the Health Care industry.

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  • Artificial Intelligence in the Health Care Industry: Part I

    Artificial Intelligence in the Health Care Industry: Part I

    In this brief discussion, Tony Ettwein, Managing Expert, Quality Center of Excellence, looks at the growth of AI, including its use in the health care industry.

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  • Understanding Clinical Trial Disclosures

    Understanding Clinical Trial Disclosures

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  • Risk Management and the Iron Triangle

    Risk Management and the Iron Triangle

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  • The Growing Field of Regulatory Policy & Intelligence

    The Growing Field of Regulatory Policy & Intelligence

    Anne Marie Finley, Managing Expert, YourEncore Regulatory Center of Excellence defines Regulatory Policy & Intelligence in Part 2 of her Expert Q&A.

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  • Defining Regulatory Policy & Intelligence

    Defining Regulatory Policy & Intelligence

    Anne Marie Finley, Managing Expert, YourEncore Regulatory Center of Excellence defines Regulatory Policy & Intelligence in Part 1 of her Expert Q&A.

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  • Understanding the RTF Letter - White Paper

    Understanding the RTF Letter - White Paper

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  • Strategic Planning in Clinical Trials and Drug Supply

    Strategic Planning in Clinical Trials and Drug Supply

    Jason Nolte, Clinical subject matter expert, discusses the importance of strategic planning teams and what they must utilize to stay relevant in the Clinical Trial & Drug Supply industry.

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  • Bioethics: Application and Implementation

    Bioethics: Application and Implementation

    In this Expert Q&A session, Luann Van Campen, Ph.D., M.A., and Don Therasse, M.D., provide valuable insights into the implementation of bioethics best practices within life sciences organizations.

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  • The Clinical Development Plan - Ensuring Success; Part 1: Developing the Clinical Strategy

    The Clinical Development Plan - Ensuring Success; Part 1: Developing the Clinical Strategy

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