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Construct and manage the technical file and design (GlobalCompliancePanel)
How to survive a DEA inspection series: due dilige (online compliance panel)
AVIANA Uganda 2012 (Aviana exhibitions inc)
AVIANA Uganda 2012 (Aviana exhibitions inc)
Pharmaceutical and biologics facility design (GlobalCompliancePanel)
21 CFR Part 11: Complying with Part 11 Regulation (GlobalCompliancePanel)
Aspects to consider for clean room qualification (GlobalCompliancePanel)
Key factors to write an effective SOP (GlobalCompliancePanel)
Best practices compliant with the FDA regulations (online compliance panel)
Pharmaceutical water system sampling (GlobalCompliancePanel)
Avoiding an FDA warning letter with a strong CAPA (GlobalCompliancePanel)
Design History File (DHF), Device Master Record (GlobalCompliancePanel)
The investigational medicinal product dossier (GlobalCompliancePanel)
Design control for professionals (GlobalCompliancePanel)
Implementing medical device complaint handling (GlobalCompliancePanel)
Anatomy of a medical device Inspection (Online Compliance Panel)
Configuration management and change control (GlobalCompliancePanel)
Combination products - FDA's proposed rule (GlobalCompliancePanel)
Statistical procedures needed for compliance (GlobalCompliancePanel)
IFRS - What is it and how do we implement it? (Online Compliance Panel)
Creating the lean physician practice - Webinar (MentorHealth)
Lyophilization Process Development (GlobalCompliancePanel)
Process validation principles and protocols (GlobalCompliancePanel)
cGMP for medical devices including In Vitro Diagno (Online Compliance Panel)
FDA guidance regarding clinical trials for foods (GlobalCompliancePanel)
Obtaining an FDA investigational device exemption (GlobalCompliancePanel)
Elements of an effective case review process (MentorHealth)
Current good manufacturing practice for medical (GlobalCompliancePanel)
Good deviation practice - what you need to know (GlobalCompliancePanel)
FDA inspections - do's and don'ts (GlobalCompliancePanel)
Incident response - are you ready? (MentorHealth)
Product hazard analysis and risk management (GlobalCompliancePanel)
Ensuring integrity and security of records (GlobalCompliancePanel)
Auditing analytical laboratories - FDA compliance (GlobalCompliancePanel)
The science of safe patient-centred care (MentorHealth)
Managing your medical device reporting (GlobalCompliancePanel)
Hazard control and risk assessment (MentorHealth)
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