Healthcare Calendar in South Africa

All events | Industry events | Workshops | Other

September - 2010 >>
Monday	Tuesday	Wednesday	Thursday	Friday	Saturday	Sunday
		1	2	3 Seminar for therapists (Client Vision Training)	4	5
6	7	8 Engineering and laboratory mythology (ComplianceOnline) Effective/essential CA/PA process to avoid FDA 483 (GlobalCompliancePanel) KZN NGOs/CSI Conference (Yellodot) Medical waste conference (Mogorosi Communications)	9 KZN NGOs/CSI Conference (Yellodot) Medical waste conference (Mogorosi Communications) Write an effective standard operating procedure (ComplianceOnline) Verification of pharmacopeia methods - webinar (GlobalCompliancePanel) Signal detection and data mining (GlobalCompliancePanel) Learning from recent FDA warning letters (GlobalCompliancePanel)	10	11	12
13	14 Analytical program to support drug development (ComplianceOnline) Understand acceptance activities - medical devices (GlobalCompliancePanel) Physical properties analytical/screening technique (GlobalCompliancePanel) Auditing API manufacturers and suppliers (GlobalCompliancePanel)	15 Troubleshooting ethylene oxide processes (GlobalCompliancePanel)	16 Law enforcement and pain management (GlobalCompliancePanel) FDA requirements for device labeling: development (GlobalCompliancePanel)	17	18	19
20	21 Why medical device companies receive warnings (GlobalCompliancePanel) Quality by design - QbD and analytical methods (GlobalCompliancePanel) Auditing computer system calidation materials (GlobalCompliancePanel) Managing IDE - investigational device exemption (GlobalCompliancePanel)	22 Stability program to support shipping (ComplianceOnline) The cosmetic-cosmeceutical distinction (GlobalCompliancePanel) Compiling design history file/technical file (GlobalCompliancePanel) Preparing for FDA inspections (GlobalCompliancePanel)	23 Developing/implementing effective product specs (GlobalCompliancePanel) Environmental and product compliance (GlobalCompliancePanel)	24	25	26
27	28 Outsourced processes and ISO 9001:2008 (GlobalCompliancePanel) Robust process validation for medical devices (GlobalCompliancePanel) Preparing for and surviving an FDA Inspection (GlobalCompliancePanel)	29 The FDA Tripod - Clinical Trial Regulations (GlobalCompliancePanel)	30 Managing Product Medical Device Recall Efficiently (GlobalCompliancePanel) Development/management/operation (GlobalCompliancePanel)