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New changes to HIPAA: The latest changes (GlobalCompliancePanel)
Design history file - DHF/Device master record (GlobalCompliancePanel)
Reprocessing re-usable medical devices (GlobalCompliancePanel)
How to prepare and submit a bullet proof 510(k) (GlobalCompliancePanel)
Designing and implementing the quality system (GlobalCompliancePanel)
Legal risks in social media for healthcare provide (GlobalCompliancePanel)
Analytical instrument and equipment qualification (GlobalCompliancePanel)
Assessing GCP compliance in clinical trial audits (GlobalCompliancePanel)
Hazard analysis vs. FMECA – differences and common (GlobalCompliancePanel)
Validating Excel and Word applications documents (GlobalCompliancePanel)
Utilizing good requirements as a foundation (GlobalCompliancePanel)
Excel spreadsheets and FDA device regulations (GlobalCompliancePanel)
Operational risk management: Ensuring safety (GlobalCompliancePanel)
Internal audits: Maintaining your quality systems (GlobalCompliancePanel)
Food safety management systems - ISO 22000:2005 (GlobalCompliancePanel)
Conference on Indian medical devices and plastics (Classic Computer Services)
Conference on Indian medical devices and plastics (Classic Computer Services)
Controlled substances and the pharmacist (GlobalCompliancePanel)
Introduction to investment risk - credit/market (GlobalCompliancePanel)
Medical device reporting regulations and violation (GlobalCompliancePanel)
Understanding the technical requirements of 21 CFR (GlobalCompliancePanel)
Electronic raw data in regulated environments (GlobalCompliancePanel)
Water system biofilm control and microbial monitor (GlobalCompliancePanel)
21 CFR part 11: complete manual for compliance (GlobalCompliancePanel)
Complying with HIPAA security rules (GlobalCompliancePanel)
Using foreign trial data in NDA approval process (GlobalCompliancePanel)
Avoiding FDA 483 observations (GlobalCompliancePanel)
Medical device changes and the 510(k) (GlobalCompliancePanel)
Practical laboratory statistics - webinar (GlobalCompliancePanel)
International financial reporting standards (GlobalCompliancePanel)
Why is CAPA so cited in medical device inspection (GlobalCompliancePanel)
21 CFR part 11 - compliance for electronic records (GlobalCompliancePanel)
Cleanroom a HEPA filter testing/certification (GlobalCompliancePanel)
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