Webinar Recordings
Medical Device Reporting: Best Practices and Common Pitfalls – Webinar Recording/Transcript
$287.00
CDER’s Priorities for 2022: What You Must Know About New Guidance and Program Plans – Webinar Recording/Transcript
$287.00
Real-World Evidence in Medical Device Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
Communicating Directly with Consumers on Social Media: What You Must Know About FDA and FTC Ad and Promo Rules – Webinar Recording/Transcript
$287.00
FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers
$287.00
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
$287.00
Prepare Your Drug/Biologics Facility for the New FDA Inspection Model: Will It Be Remote, In-Person or Hybrid? – Webinar Recording/Transcript
$287.00
FDA Medical Device Inspections in the Postpandemic World: Are You Ready for New Approaches and Methods? – Webinar Recording/Transcript
$287.00
Supply Chain Solutions: How the Pharmaceutical Industry Can End In-Bound Issue – Webinar Recording/Transcript
$287.00
