Regulatory guidelines for QMS 2022 - QMS Quality Management System

OVERVIEW
Some regulatory guidelines mention the need for a QMS. But every company should have a library for its biggest asset – the knowledge of the employees. The reason to have a QMS is not to satisfy the regulators, but for any employee to find the reason for doing the work they should do and how it is connected to the rest of the company.
Any of you who wants to do a good job needs to know the reasons, rules, and standards in this company and on that job. A QMS is therefore essential, and this webinar can help you to understand the basics of a QMS and how important your part is in saving the company resources and being compliant.
WHY SHOULD YOU ATTEND?
The cost of not finding something at an inspection, or of missing knowledge can be staggering. Having to do things a second time, because of lost know-how, costs resources. Any auditor or inspector can ask you to show, why you do what you do in comparison to the framework of the company.
Most companies working in the health area have defined the safety of patients, and their clients, as one of their main goals within their overall policy. This is The base-stone; everything within this company is build-on.
AREA COVERED
Overview and Definitions
The reasons why connecting something and what for
The two pillars of the company’s knowledge or actual asset
Common mistakes and today's problems
Best practices or the ideal setup
Questions
WHO WILL BENEFIT?
Quality Assurance Professionals
Validation Professionals
Standards and SOP Professionals
Data Management Professionals
Electronic Systems Developers
The inspection readiness team
Clinical and medical device Operations Professionals
Project leaders
SPEAKER PROFILE
Willi Ramseier is currently the owner and director of QVRAM GmbH of Basel, Switzerland. As an expert in quality assurance, system validation, risk awareness, and management, Ramseier is a reputed trainer, mentor, and quality compliance officer.
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