All events | Industry events | Workshops | Other
Submit an event
Let's do Biz
Residual risk and risk based verification (GlobalCompliancePanel)
Excel spreadsheet validation to eliminate 483s (GlobalCompliancePanel)
Water system investigation (GlobalCompliancePanel)
FDA bioresearch monitoring - BIMO inspection (GlobalCompliancePanel)
Statistical procedures needed for compliance (GlobalCompliancePanel)
Prepare and submit 510(k) premarket notification (GlobalCompliancePanel)
Prepare and submit 510(k) premarket notification (GlobalCompliancePanel)
Compliance processes for life science products (GlobalCompliancePanel)
Root Cause Analysis (GlobalCompliancePanel)
Root Cause Analysis (GlobalCompliancePanel)
China - Compliance processes for life science (GlobalCompliancePanel)
Tougher FDA cGMP compliance audits (GlobalCompliancePanel)
EU medical device classification (GlobalCompliancePanel)
Six systems approach to pharmaceuticals (GlobalCompliancePanel)
Tougher FDA cGMP compliance audits and enforcement (GlobalCompliancePanel)
EU medical device classification (GlobalCompliancePanel)
Six systems approach to pharmaceutical cGMP (GlobalCompliancePanel)
Key steps to avoid 483 warning letters (GlobalCompliancePanel)
Incorporating six Sigma DMAIC into CAPA (GlobalCompliancePanel)
Creating effective master validation plans (GlobalCompliancePanel)
Incorporating six sigma DMAIC into CAPA (GlobalCompliancePanel)
Regulatory compliance for dietary supplements (GlobalCompliancePanel)
Regulatory compliance for dietary supplements (GlobalCompliancePanel)
Hazard analysis - a practical guide (GlobalCompliancePanel)
Co-development of targeted therapeutics (GlobalCompliancePanel)
Hazard analysis - a practical guide (GlobalCompliancePanel)
Co-development of targeted therapeutics (GlobalCompliancePanel)
Complaint handling in compliance with FDA (GlobalCompliancePanel)
How to successfully prepare to host the FDA (GlobalCompliancePanel)
Complaint handling in compliance with FDA and ISO (GlobalCompliancePanel)
How to prepare and host an FDA inspection (GlobalCompliancePanel)
Strategia - Strategic Conversation (Strategnos)
Update on unique device identifier (GlobalCompliancePanel)
FMEA and risk management for medical devices (GlobalCompliancePanel)
Unique device identifier for device manufacturers (GlobalCompliancePanel)
Deviation management system (GlobalCompliancePanel)
FDA guidance regarding clinical trials for foods (GlobalCompliancePanel)
FDA inspections - do's and don'ts (GlobalCompliancePanel)
Deviation management system (GlobalCompliancePanel)
FDA Guidance Regarding Clinical Trials for Foods (GlobalCompliancePanel)
FDA Inspections - do's and don'ts (GlobalCompliancePanel)
Water system biofilm control (GlobalCompliancePanel)
Water system biofilm control (GlobalCompliancePanel)
Successful 510(k) submission - contents and format (GlobalCompliancePanel)
Hear for life (Origins Centre)
Zim-Afro medical and health expo 2012 (Zim-Afro)
Zim-Afro medical and health expo 2012 (Zim-Afro)
Statistical concepts of process validation (GlobalCompliancePanel)
Anticipated changes to the EU medical device (GlobalCompliancePanel)
OSHA injury and illness record keeping (MentorHealth)
IND Submission for a 505(b)(2) Product (Online Compliance panel)
Statistics for quality control and assurance (GlobalCompliancePanel)
Zim-Afro medical and health expo 2012 (Zim-Afro)
Statistics for quality control and assurance (GlobalCompliancePanel)
Submit an event

