Company Info





Home > Archived Webinars
Choose a sub category:
Diagnostic Medical Device
Pharmaceutical Drug Delivery
Food and Beverage Combination Products
Sort By:
Page of 25
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
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
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 Leveraging KOL Expertise in Women’s Health: Aligning Pre-Launch Marketing Strategies with Thought Leadership
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
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 Data Integrity and Compliance in Pharmaceutical Manufacturing
Our Price: $395.00
Our Price: $395.00
Our Price: $395.00
Digital Health Technologies: Navigating the Intersections of Innovation and Regulation Identifying Adulterated Botanical Ingredients- A Framework to Protect Industry from Fraudulent Materials Data Integrity and Compliance in Pharmaceutical Manufacturing