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Professional Courses | List of Training Courses - Seminars

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successfully completed seminar on "The New Clinical Trials Regulation 2017"

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How to build a complete Safety, Health & Environment Management System 2017

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successfully completed seminar on Statistics for the Non-Statistician

01:29:36

Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans

01:19:59

Requirements Contents and Options : The 510k Submission

01:18:50

Statistical Concepts of Process Validation

01:12:06

Medical Devices - ISO 14971 : Risk Management

01:06:19

What to do during recalls, removals, and market corrections

01:11:27

Purchasing and Supplier Controls in the Medical Device Industry

01:08:12

Protocols for Medical Devices & Process Validation Principles

01:28:00

Process Validation Procedure for Medical Device Manufacturers

01:17:22

Outsourced processes and ISO 9001:2008

59:53

Medical Device Design Control

01:09:52

Medical Device Complaint Handling Systems

01:13:42

Medical Device Adverse Event Reporting in EU, US and Canada

01:05:37

Managing the Medical Device Supply Chain

01:08:18

How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

01:03:26

Ensure data integrity and subject safety in clinical research

01:10:24

FDA Requirements for Device Labeling

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How to prepare for an FDA inspection

01:24:27

Understand the FDA device regulations related to Excel spreadsheets

01:05:08

Equipment Validation, Tracking, Calibration, and Preventive Maintenance

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How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner

01:09:32

Regulatory Documents Explained - DHF, DMR, DHR and TF

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FDA QSR Requirements for DMR & DHR

01:17:36

Recalls, Corrections and Removals (Devices)

01:17:15

Effective Audit Program for both internal and external Processes

01:02:57

FDA Quality Systems Regulation Requirements - Regulatory Documents Explained

01:16:37

cGMP for Medical Devices Including IVDs

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Importance, Requirements, and Elements of a CAPA Program

01:07:58

How to Prepare a 510(k) Quality Submission

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Common Regulatory and company requirements

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Allergen control

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Statistical methods used to calculate sample sizes

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Supplier Risk Management

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Statistical Process Control and Trending Analysis

01:03:07

HACCP Validation and Verification

01:09:35

Good Laboratory Practices for Food Processing Quality Labs

01:22:35

Cleaning and Sanitation Training for Food Processors

01:31:04

South Korea: Navigating the Clinical Trial and Regulatory Environment

46:45

Premarket Approval (PMA) Agreement with FDA for the Medical Device Companies

01:24:22

New EU Pharmacovigilance Directive and Regulations

01:10:36

Introduction to Design of Experiments and ANOVA

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FDA's current thinking on cGMP compliance for Phase I Investigational Drug and Biologic products

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Avoiding Statistical Pitfalls during Method Validation

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Leadership in Manufacturing Contamination Control

01:47:38

Water System Biofilm Control and Microbial Monitoring Myths

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Premarket Approval PMA Agreement with FDA for the Medical Device Companies

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Laboratory Water Systems Necessary Water Specifications and Validation Challenges -NetZealous LLC

01:47:05

Key Concepts in Successful Water System Sanitization - NetZealous LLC DBA GlobalCompliancePanel

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NetZealous LLC an Innovative Professional Training Provider

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Supplier and Internal Auditing

01:05:08

Quality System Records Origin and Controls

01:08:12

Process Validation Principles and Protocols for Medical Devices

01:28:00

Process Validation for Medical Device Manufacturers

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Medical Device Complaint Handling: MDR, Reports of Removals and Corrections

01:01:53

GMP Training for Manufacturing and Administration Personnel

01:05:08

Equipment Validation, Tracking, Calibration, and Preventive Maintenance

01:09:32

DHF, DMR, DHR and TF Regulatory Documents Explained