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Compliance Online - Market Research Reports

ComplianceOnline is an industry focused portal, developed for the practitioners of quality and regulatory compliance. They are focused on enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

Medical Device Cybersecurity Risk Management Training - Product Thumbnail Image

Medical Device Cybersecurity Risk Management Training

  • Training
  • 3 Hours
  • Global
Risk Management for Medical Devices per ISO 14971 2019 - Product Thumbnail Image

Risk Management for Medical Devices per ISO 14971 2019

  • Training
  • 60 Minutes
  • Global
How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity - Product Thumbnail Image

How to Comply with FDA Regulations for Tobacco-Related Products: Computer System Validation, 21 CFR Part 11, & Data Integrity

  • Training
  • 90 Minutes
  • Global
US FDA's AI Framework for Medical Devices - Product Thumbnail Image

US FDA's AI Framework for Medical Devices

  • Training
  • 90 Minutes
  • United States
Predicting Product Life Using Reliability Analysis Methods - Product Thumbnail Image

Predicting Product Life Using Reliability Analysis Methods

  • Training
  • 90 Minutes
  • Global
NEW Reclamation Process (effective 1-1-23) with ACH Federal Government Reclamations, plus guidance on Misdirected Payments and DNE's (Death Notification Entries) - Product Thumbnail Image

NEW Reclamation Process (effective 1-1-23) with ACH Federal Government Reclamations, plus guidance on Misdirected Payments and DNE's (Death Notification Entries)

  • Training
  • 90 Minutes
  • Global
Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data - Product Thumbnail Image

Good Documentation Practice (GDP) and FDA Validation Compliance for Regulated Computer Systems and Data

  • Training
  • 90 Minutes
  • Global
Risk Management of Raw Materials in a GMP Environment - Product Thumbnail Image

Risk Management of Raw Materials in a GMP Environment

  • Training
  • 90 Minutes
  • Global
Test Method / Design Verification and Validation - Product Thumbnail Image

Test Method / Design Verification and Validation

  • Training
  • 90 Minutes
  • Global
Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology - Product Thumbnail Image

Computer System Validation (CSV) vs. Computer System Assurance (CSA): Aligning the Agile Methodology to the GAMP®5 "V" Model and System Development Life Cycle (SDLC) Methodology

  • Training
  • 120 Minutes
  • Global
The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process - Product Thumbnail Image

The 510(k), IDE, Q-Sub, De Novo, and PMA Submission and Approval Process

  • Training
  • 90 Minutes
  • Global
Impact Assessment for Change Control - Product Thumbnail Image

Impact Assessment for Change Control

  • Training
  • 60 Minutes
  • Global
Conducting Effective Mock FDA Inspections - Product Thumbnail Image

Conducting Effective Mock FDA Inspections

  • Training
  • 90 Minutes
  • Global
Normality Testing: Applications and Issues - Product Thumbnail Image

Normality Testing: Applications and Issues

  • Training
  • 90 Minutes
  • Global
Accident/Incident Investigation and Root Cause Analysis - Product Thumbnail Image

Accident/Incident Investigation and Root Cause Analysis

  • Training
  • 60 Minutes
  • Global
USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms - Product Thumbnail Image

USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms

  • Training
  • 90 Minutes
  • Global
Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366 - Product Thumbnail Image

Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366

  • Training
  • 90 Minutes
  • Global
GAMP Data Integrity 21 CFR Part 11 Training Course - Product Thumbnail Image

GAMP Data Integrity 21 CFR Part 11 Training Course

  • Training
  • 90 Minutes
  • Global
Creating Powerful PowerPoint Decks - Product Thumbnail Image

Creating Powerful PowerPoint Decks

  • Training
  • 90 Minutes
  • Global
Creating a Good Design History File (DHF) for Audit Success - Product Thumbnail Image

Creating a Good Design History File (DHF) for Audit Success

  • Training
  • 60 Minutes
  • Global
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