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MEETINGS - TUV Akademie is organising the following series of seminars for FDA-regulated industries (Germany) October - December 1995:

This article was originally published in Clinica

Executive Summary

TUV Akademie is organising the following series of seminars for FDA-regulated industries in Munich, Germany, later this year: Medical Device Regulatory Affairs (October 17th-18th); Understanding the Medical Device GMP and Regulations (October 19th-20th); General Concepts of Process Validation (November 6th-7th); How to Manage an Inspection by the FDA (November 8th-9th); Fundamentals of Pharmaceutical Regulatory Affairs (December 11th-12th); Understanding the Pharmaceutical GMP and Regulations (December 13th-14th). For further details, contact: Frau Sebert, TUV Akademie, Westendstrasse 199, 80686 Munich, Germany. Tel: +49 (89) 5791 1820. Fax: +49 (89) 5791 2247.

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