GlobalCompliance Panel
GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.
Professional Courses | List of Training Courses - Seminars
successfully completed seminar on "The New Clinical Trials Regulation 2017"
How to build a complete Safety, Health & Environment Management System 2017
successfully completed seminar on Statistics for the Non-Statistician
Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
Requirements Contents and Options : The 510k Submission
Statistical Concepts of Process Validation
Medical Devices - ISO 14971 : Risk Management
What to do during recalls, removals, and market corrections
Purchasing and Supplier Controls in the Medical Device Industry
Protocols for Medical Devices & Process Validation Principles
Process Validation Procedure for Medical Device Manufacturers
Outsourced processes and ISO 9001:2008
Medical Device Design Control
Medical Device Complaint Handling Systems
Medical Device Adverse Event Reporting in EU, US and Canada
Managing the Medical Device Supply Chain
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Ensure data integrity and subject safety in clinical research
FDA Requirements for Device Labeling
How to prepare for an FDA inspection
Understand the FDA device regulations related to Excel spreadsheets
Equipment Validation, Tracking, Calibration, and Preventive Maintenance
How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner
Regulatory Documents Explained - DHF, DMR, DHR and TF
FDA QSR Requirements for DMR & DHR
Recalls, Corrections and Removals (Devices)
Effective Audit Program for both internal and external Processes
FDA Quality Systems Regulation Requirements - Regulatory Documents Explained
cGMP for Medical Devices Including IVDs