Upcoming FDA cGMP Expertbriefings
May 22nd, 2013 // 5:12 pm @ jmpickett
Upcoming FDA cGMP Expertbriefings.com Webinars for 2013 include:
- May 30 – How to Survive PREDICT – FDA’s New Import Screening Program
- May 30 – The Essentials of Complaint Handling and Post Market Management – How to Comply With Global Regulatory Requirements
- May 30 – Audit Your Lab Like an FDA Auditor – A Roadmap to cGMP Lab Compliance
- June 4Â -Â How to Prepare Yourself for 21 CFR Part 11 Inspections
- June 5 – How to Bulletproof Your 510(k) Submission
- June 11 – FSMA Landmines That Affect the International Food Supply Chain
- June 12 – Spend $500K on Compliance or $300 Million on Consent Decree? – Essential cGMP Compliance Tips for Sr. Management
- June 12 – Avoiding Warning Letter Disasters With a Strong cGMP and GCP Quality Agreement
- June 12 – FDA Recall Chief Update – How to Design a Bulletproof Recall Strategy
- June 18 – FDA Chief Counsel Report – How to Deal With and Avoid Warning Letters
- June 18 – Avoid the CDRH eCopy Confusion – How to Prepare a Compliant eCopy Submission
- June 19 – Breaking Regulatory Update for Life Science Firms – UFA Requirements for eCTDs
Updated Daily – Read our latest FDA, cGMP Compliance News
