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The Master of Good Manufacturing Practice course provides up to date and in depth good manufacturing practice (GMP) knowledge within the pharmaceutical, biotechnology and medical device industries. The course provides critical knowledge of legislation relating to the registration, manufacture, storage and supply of licensed therapeutic goods; GxP and quality systems compliance; and the concepts of quality management, risk management, quality assurance and quality control within this heavily regulated industry – all essential ingredients for career development.

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Good Manufacturing Practices (GMP) constitute an international set of guidelines for the manufacture of drugs and medical devices in order to ensure the production of quality products. GMP protocols are being adopted and followed in over 100 countries including US, Japan, EU & Australia.

University of Technology Sydney has partnered with SeerPharma, Asia Pacific’s leading provider of technical compliance & QA knowledge to deliver innovative, university-accredited graduate programs in Good Manufacturing Practices.

To help students from India to access these courses, SeerPharma has selected Labnetworx to be its partner for India. SeerPharma has been delivering these courses in Australia for the last 12 years and the majority of students who have completed their Masters Degree during this time are from India. We therefore already have a strong connection with India. 

These programs are best suited for students who seek in-depth knowledge of regulations, compliance, process development and quality assurance in the pharmaceutical, medical device & biotechnology sectors.  Students will gain expert knowledge of Quality and GMP to meet TGA, FDA, EU & PIC/S requirement. These factors are important for career development in the pharmaceutical industry both in Australia and globally. Typically, students who graduate find jobs in Quality Assurance, Quality Control, Production, Validation, Development and even Regulatory departments. The programs are unique in Australia and the Asia-Pacific region and will help students to build relationships with pharmaceutical industry.

India is emerging as a powerhouse in the pharma and related industries. Its companies and their employees will benefit from this course conducted by SeerPharma’s experienced personnel. 


What is GMP?

Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards.

Why is GMP important?

Poor quality medicines are not only a health hazard, but a waste of money for both governments and individual consumers.
A poor-quality medicine may contain toxic substances that have been unintentionally added. A medicine that contain s little or none of the claimed ingredient will not have the intended therapeutic effect.

Is GMP necessary if there is a quality control laboratory?

Yes. Good quality must be built in during the manufacturing process, it cannot be tested into the product afterwards. GMP prevents errors that cannot be eliminated through quality control of the finished product. Without GMP it is impossible to be sure that every unit of a medicine is of the same quality as the units of medicine tested in the laboratory.

Admission requirements 

Applicants must have completed a UTS recognised bachelor’s degree, or an equivalent or higher qualification, or submitted other evidence of general and professional qualifications that demonstrates potential to pursue graduate studies. 

The above qualifications must be in one of the following related disciplines: > Natural and Physical Sciences > Pharmacy > Engineering and Related Technologies.

For more information about this course, please visit the University of Technology Sydney website.

UTS CRICOS Provider No: 00099F

For admission related queries from India, please contact Labnetworx at:

Phone: +91-85273-17888


To know more about the course & college please click here

Success Stories

The International experience: Kiran’s GMP studies at UTS