Hi ! I am applying to an Endeavour Scholarship - Australia. I really need some feedback about the following text. Can you please help me, I really appreciate it. Thank you so so much.
Good Manufacturing Practice (GMP) is an international standard covering a set of regulations for manufacturing operations that a pharmaceutical company has to follow to assure that the drugs are of high quality and do not pose any risks to the patients or public. To keep up with the growth pace of the industry of pharmaceutics, University Technology Sydney (UTS) has delivered a coursework - Master of GMP - which primarily focuses on the up-to-date understandings of legislation relating to the registration, manufacture, storage and delivery of licensed therapeutic goods, as well as how to become an outstanding administrator in quality assurance, risk management and quality control within the industry of pharmaceutical organizations.
Being a Quality Assurance Analyst of a pharmaceutical company, I am thoroughly conscious of the importance of elements and obligations for manufacturers to implement or maintain GMP compliance. Despite 25 years of experience in medicine manufacturing, my current employer still has challenges in quality management system such as computerized documentation, antimicrobial cross-contamination control, sanitation for premises, and other operation-related issues. Therefore, I nurture a strong desire that I manage to solve GMP-based problems which prevents us from entering U.S.A and Australia market where PIC/S-GMP and US.FDA-GMP - higher standards than WHO-GMP - are required. After completion of the course, I will be able to optimize the GMP compliance in pharmaceutical manufacturing environment systematically and professionally according to strict requirements provided by the regulatory authorities in various regions such as TGA-Australia (Therapeutic Goods Administration), FDA-USA (Food and Drug Administration) and EMA-Europe (European Medical Agency).
In UTS, students will have opportunities to take two internships for two research projects at SeerPharma- an Asia-Pacific's Leader in Quality Assurance and GMP solutions. This makes this programme more practice-based and helps students develop their career paths in drug manufacturing industry.
drug manufacturing quality
Good Manufacturing Practice (GMP) is an international standard covering a set of regulations for manufacturing operations that a pharmaceutical company has to follow to assure that the drugs are of high quality and do not pose any risks to the patients or public. To keep up with the growth pace of the industry of pharmaceutics, University Technology Sydney (UTS) has delivered a coursework - Master of GMP - which primarily focuses on the up-to-date understandings of legislation relating to the registration, manufacture, storage and delivery of licensed therapeutic goods, as well as how to become an outstanding administrator in quality assurance, risk management and quality control within the industry of pharmaceutical organizations.
Being a Quality Assurance Analyst of a pharmaceutical company, I am thoroughly conscious of the importance of elements and obligations for manufacturers to implement or maintain GMP compliance. Despite 25 years of experience in medicine manufacturing, my current employer still has challenges in quality management system such as computerized documentation, antimicrobial cross-contamination control, sanitation for premises, and other operation-related issues. Therefore, I nurture a strong desire that I manage to solve GMP-based problems which prevents us from entering U.S.A and Australia market where PIC/S-GMP and US.FDA-GMP - higher standards than WHO-GMP - are required. After completion of the course, I will be able to optimize the GMP compliance in pharmaceutical manufacturing environment systematically and professionally according to strict requirements provided by the regulatory authorities in various regions such as TGA-Australia (Therapeutic Goods Administration), FDA-USA (Food and Drug Administration) and EMA-Europe (European Medical Agency).
In UTS, students will have opportunities to take two internships for two research projects at SeerPharma- an Asia-Pacific's Leader in Quality Assurance and GMP solutions. This makes this programme more practice-based and helps students develop their career paths in drug manufacturing industry.
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