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Die Veranstaltung umfasst folgende Beiträge:

Nr. Thema Kurzf. Folien
10694
Pharmaceutical Ingredients-regulatory expectations-40
10695
Update on EC Certain Excipients Legislation-41
10696
FDA Update on the Control of Excipients-37
10697
IPEC Guide as an appropriate guidance for Excipients manufacturers-Comparison to ICH Q7-39
10698
Design of an effective compliance programme for Excipients manufacturing-16
10699
Excipients certification - schemes, standards, value-40
10700
PS_01: Auditing an Excipients Manufacturer-16
10701
PS_02_Changes Control Management-18
10702
PS_03_Excipients for use in parenteral products-38
10703
MHRA voluntary Inspection scheme-36
10704
How to design risk based manufacturing strategies to meet costumers GMP expectations-46
10705
The role of quality agreements in Excipients supply-22
10706
Excipients pedigree - Repackaging, relabeling, recertification of excipients-26