GlobalCompliancePanel events

GlobalCompliancePanel deliver several regulatory and compliance training events throughout the year. Here are their latest listings:

Event date
20 Mar 2012USFDA & EU Essentials of Drug Safety and Pharmacovigilance - India Seminar 2012 at Mumbai (Added 03 Feb 2012)
20 Mar 2012The 510(k) Submission: Requirements, Contents, and Options (Added 23 Jan 2012)
13 Mar 2012Auditing Computer Systems for FDA and International Compliance (Added 23 Jan 2012)
06 Mar 201221 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits (Added 23 Jan 2012)
20 Mar 2012Excel Spreadsheet Validation to Eliminate 483s (Added 23 Jan 2012)
21 Mar 2012Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements (Added 23 Jan 2012)
13 Mar 2012Changes in the EU Medical Device Directives; 2010 Modifications and the 2012 Recast of the MDD Directives (Added 23 Jan 2012)
24 Jan 2012Excel Spreadsheet Validation for FDA 21 CFR Part 11 (Added 20 Dec 2011)
21 Feb 2012Risk Assessment - Compliance Using Easy To Fill Out Documentation (Added 20 Dec 2011)
01 Feb 2012Efficient Computer System Validation - 10 Easy Steps (Added 20 Dec 2011)
22 Feb 2012Implement a Tougher Supplier Audit Program (Added 20 Dec 2011)
08 Feb 2012Product Risk Management Under ISO 14971 and FDA-ICH Q9 (Added 20 Dec 2011)
24 Jan 2012Excel Spreadsheet Validation for FDA 21 CFR Part 11 (Added 20 Dec 2011)
21 Feb 2012Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA (Added 20 Dec 2011)
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