ECA - Inspection Management (How to pass EU and FDA Inspections)

Art-No.: A-232
Date: 06 - 08 November 2018

Price: EUR 380,-

The Conference folder includes the following topics:

No. Topic Summary Pages
1914The Challenges of GMP Audits vs. Inspections027
1915Typical Compliance Issues038
1916Case Study: Proactive Compliance and Inspection Management - it's more than Self Inspection Workshop: An Inspection Management Risk Model 016
1917The View of a former EU Inspector: Authority Expectations - some practical examples 026
1918The View of a former FDA-inspector: The FDA Inspection System 052
1919What makes a good Inspector017
1920Workshop Session " Preparing for a Regulatory Inspection " Risk Analysis related to the Inspection and Findings " Data Integrity 0144
8405The MOCK-Inspection: Auditing your Company to prepare for international Inspections 032
10190Preparation and Management of Regulatory Inspections034
11364Expactations from Inspectorates worldwide053
13670The juristic Perspective - how Legal Department can support QA021

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