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Opportunities in ASC to Navigate the Future of Medical Device Reimbursement Decision Criteria: New FDA Guidance Impacting the Requirement for 510(K) Clearance of Modified Devices Implementing New Responsibilities for Economic Operators under the EU MDR
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Opportunities in ASC to Navigate the Future of Medical Device Reimbursement Decision Criteria: New FDA Guidance Impacting the Requirement for 510(K) Clearance of Modified Devices Implementing New Responsibilities for Economic Operators under the EU MDR
Best Practices for Medical Device Human Factors Post-Market Surveillance Activities Unannounced Audit Case Study: A Medical Device Manufacturers Experiences FDA Regulatory Due Diligence in Mergers and Acquisitions for Medical Device Companies
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Best Practices for Medical Device Human Factors Post-Market Surveillance Activities Unannounced Audit Case Study: A Medical Device Manufacturers Experiences FDA Regulatory Due Diligence in Mergers and Acquisitions for Medical Device Companies
Leveraging KOL Expertise in Women’s Health: Aligning Pre-Launch Marketing Strategies with Thought Leadership Digital Health Technologies: Navigating the Intersections of Innovation and Regulation Identifying Adulterated Botanical Ingredients- A Framework to Protect Industry from Fraudulent Materials
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Leveraging KOL Expertise in Women’s Health: Aligning Pre-Launch Marketing Strategies with Thought Leadership Digital Health Technologies: Navigating the Intersections of Innovation and Regulation Identifying Adulterated Botanical Ingredients- A Framework to Protect Industry from Fraudulent Materials