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Webinar Recordings

Pamela Forrest  -Aqua 500

Medical Device Reporting: Best Practices and Common Pitfalls – Webinar Recording/Transcript

$287.00
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Howard Sklamberg and Abraham Gitterman-600red

FDA’s New Distributor Licensing Standards – Webinar Recording/Transcript

$287.00
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Radhika Rajagopalan, Ph.D. - green 600

CDER’s Priorities for 2022: What You Must Know About New Guidance and Program Plans – Webinar Recording/Transcript

$287.00
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Kristin Zielinksi Duggan Aqua 500

Real-World Evidence in Medical Device Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript

$287.00
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Kellie Combs and Josh-Oyster - 500blue

Communicating Directly with Consumers on Social Media: What You Must Know About FDA and FTC Ad and Promo Rules – Webinar Recording/Transcript

$287.00
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Kristen Grumet - Red

FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers

$287.00
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David L. Chesney Aqua 500

Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript

$287.00
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Cynthia Schneda- Steven J. Lynn- Bob Rhoades-blue

Prepare Your Drug/Biologics Facility for the New FDA Inspection Model: Will It Be Remote, In-Person or Hybrid? – Webinar Recording/Transcript

$287.00
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Seyed Khorashahi  - red

FDA Medical Device Inspections in the Postpandemic World: Are You Ready for New Approaches and Methods? – Webinar Recording/Transcript

$287.00
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Robert Brooks, PhD - 500blue

Supply Chain Solutions: How the Pharmaceutical Industry Can End In-Bound Issue – Webinar Recording/Transcript

$287.00
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Scott R. Burger and William E. Janssen -red600

Gene & Cell Therapy Regulation: Comparability and Other New Developments – Webinar Recording/Transcript

$287.00
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Lance Shea - green600

Statistics and Data for Regulatory Professionals and Attorneys: Product Performance Evidence Made Easy – Webinar Recording/Transcript

$287.00
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