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Home > Conferences > FDA Pharmaceutical and Medical Device Training and Conference CDs & Transcripts

FDA Pharmaceutical and Medical Device Training and Conference CDs & Transcripts

Reduce Human Error on the Drug and Device Manufacturing Floor

Thursday, July 26, 2012

Medical Device Reimbursement De-Mystified
Securing Value-Based Payment for Medical Devices in Changing Times

Tuesday, July 24, 2012

Device Off-Label Promotion
Understanding What the FDA Is Looking For

Thursday, July 19, 2012

Understanding the U.S. Biosimilar Pathway in 2012
An In-Depth Look at the Debate and Its Implications

Thursday, June 28, 2012

Process Validation for Medical Devices
Understanding What the FDA Is Looking For

Tuesday, June 26, 2012

Inspectional Readiness
Are Your SMEs Prepared for A Successful FDA Visit?

Thursday, May 31, 2012

A World Apart
Understanding Differences in EU and U.S. Drug and Device Adverse Event Reporting

Wednesday, May 30, 2012

Physician Payment Sunshine Act
New January 1, 2013 Compliance Deadline — Will You Be Ready?

Wednesday, May 23, 2012

510(k) Process Changes Survival Guide
Practical Answers in 90 Minutes

Thursday, April 19, 2012

Part 806 Device Recalls
What You Should Know to Avoid Under-Reporting

Thursday, April 12, 2012

Dietary Supplement GMP Inspections and Violations
Tough Talk, Tougher Inspections on the Way

Thursday, April 5, 2012

Medical Device Complaint Management
Taming “Out of Control” Systems to Assure Compliance

Thursday, March 22, 2012

Legal and Regulatory Guide to EU’s New Pharmacovigilance Regulations
Understanding the Implications and Nuances to Assure Compliance

Tuesday, March 20, 2012

FDA Import Holds
Black Hole or Bright Spot for Managing Your Imports?

Wednesday, Feb. 29, 2012

Develop a Process Validation Roadmap
Case Studies Show How to Satisfy FDA’s Scrutiny

Tuesday, Feb. 28, 2012

FDA Pharmaceutical and Medical Device Training and Conference CDs & Transcripts

Reduce Human Error on the Drug and Device Manufacturing Floor

Medical Device Reimbursement De-Mystified Securing Value-Based Payment for Medical Devices in Changing Times

Device Off-Label Promotion Understanding What the FDA Is Looking For

Understanding the U.S. Biosimilar Pathway in 2012 An In-Depth Look at the Debate and Its Implications

Process Validation for Medical Devices Understanding What the FDA Is Looking For

Inspectional Readiness Are Your SMEs Prepared for A Successful FDA Visit?

A World Apart Understanding Differences in EU and U.S. Drug and Device Adverse Event Reporting

Physician Payment Sunshine Act New January 1, 2013 Compliance Deadline — Will You Be Ready?

510(k) Process Changes Survival Guide Practical Answers in 90 Minutes

Part 806 Device Recalls What You Should Know to Avoid Under-Reporting

Dietary Supplement GMP Inspections and Violations Tough Talk, Tougher Inspections on the Way

Medical Device Complaint Management Taming “Out of Control” Systems to Assure Compliance

Legal and Regulatory Guide to EU’s New Pharmacovigilance Regulations Understanding the Implications and Nuances to Assure Compliance

FDA Import Holds Black Hole or Bright Spot for Managing Your Imports?

Develop a Process Validation Roadmap Case Studies Show How to Satisfy FDA’s Scrutiny

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