Master pharmaceutical quality management system

Master pharmaceutical quality management system

Pharmaceutical quality management system, medical device quality management system, site quality management system

What you’ll learn

  • In this course you will master the pharma industry quality management system “QMS” which is mandatory for any kind of submission across all countries
  • Quality management system “QMS”
  • Pharmaceutical Quality management system “QMS”
  • Medical device Quality management system “QMS”
  • Site Quality management system “QMS”

This course includes:

2 hours of video
3 articles + resources
Certificate of completion


  • Laptop and willing to learn


The quality management system (QMS) is the backbone concept in the pharma industry, if you are planning to register a manufacturing site, pharmaceutical product, or medical device, in all cases, you have to be complied with the quality management system (QMS) to ensure quality, which is the major topic of concern by all health authorities globally.

The QMS is a formalized system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. The QMS will help to coordinate and direct an organization’s activities to meet customer and regulatory requirements and improve its effectiveness and efficiency on a continuous basis.

In this course we will dive deeply together into the QMS, to understand the concept behind it, the 3 levels of quality, the role of the management towards QMS, the QMS objectives, who the elements of the QMS are integrated together to come up with the final QMS.

Then we will practice QMS in the pharma industry, to understand what is the meaning and application of QMS in the pharma industry, to understand that quality is a continuous process rather than just an activity that comes after the finishing of any process in the pharma industry

quality is involved in all stages of any product Lifecycle, conations with it and going in parallel together with it.

and then will test the behavior towards the QMS, quality standards, and pharmacopeias behind it.

Then we will explore the ISO, its definition, history, development, its clauses over the years, what is new in these clauses, and finally, the ISO outcomes which are our main target in the pharma industry out of the application and be complied with ISO.

Then come to the GMP, the core concept and document of the quality for any kind of submissions in any country

and then expanding to the wider big scope of the GXP, ending with documentation, which is very crucial as the pharma industry is all about documentation and keeping records.

Then we will Cloe our course with personnel training on the QMS concepts and application, and finally process validation.

Let us prepare ourselves for the interesting dive, let’s go.

Who this course is for:

  • Pharma industry professionals, beginners and fresh graduated who area enthusiastic to start their career in the pharma industry
  • Pharma industry beginners
  • Pharma industry professionals
  • Fresh school of pharmacy graduates
  • Pharma regulatory affairs professionals


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