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A Medical Technologist, joined Grand Pacific CRO in 2017 as a senior analyst. During 2017-2021, Siribha worked as a team to conduct analysis for quantitation of drugs level in biological fluid using the liquid chromatography couple with mass spectrometry (LC/MS). She has extensive experience in bioanalysis method development and validation for drugs using LC-MS/MS. These quantitation assay methods developed are fully validated according to US-food and drug administration and European Agency Medicine guidelines and certified with ISO15189. More recently, she has started as Quality Assurance Officer. Her role includes helping with team for preparing and implementing quality assurance policies and procedures. She works closely with communication staff across the GPCRO to ensure that the GPCRO activities will work without any problems as per the expectations or requirements.
×He got PhD in Biotechnology from Chulalongkorn university Bangkok Thailand. He got collaborate scholarship program to do PhD research at Texas A&M university (Kingsville) Texas USA with funding support from National Institute of Health (NIH) USA. After graduate, he works as clinical lab consultant at private hospital in Bangkok. Then, move to pharmaceutical company as study director for PK and BABE analysis. After that, join with Mass spectrometer company as application specialist support customer in ASEAN area especially bioanalysis field, he got more than ten years experiences on biological sample analysis.
Piboon very expert on pharmaceutical analysis by using LC-MS/MS technique. Piboon was invited from university as special lecture and collaborate research with PhD student on pharmaceutical research also.
×A laboratory analyst with experience for 10 years in routine sample processing and 5 years in LC-MSMS techniques in drug monitoring and drugs level measuring in human plasma for bioequivalence study with fully validated method under USFDA and European Agency Medicine’s guideline. At Grand Pacific CRO she is a project manager-kit building for clinical study coming and laboratory services. Her responsibilities to manage kit building process to be suited with project and meet the client or sponsor’s requirement. Moreover, she has also achieve the certified by ISO15189 and ISO15190 accreditation to comply all assigned tasks in GPCRO.
×A Medical Technologist, joined Grand Pacific CRO in 2017 as a senior analyst. During 2017-2021, Siribha worked as a team to conduct analysis for quantitation of drugs level in biological fluid using the liquid chromatography couple with mass spectrometry (LC/MS). She has extensive experience in bioanalysis method development and validation for drugs using LC-MS/MS. These quantitation assay methods developed are fully validated according to US-food and drug administration and European Agency Medicine guidelines and certified with ISO15189. More recently, she has started as Quality Assurance Officer. Her role includes helping with team for preparing and implementing quality assurance policies and procedures. She works closely with communication staff across the GPCRO to ensure that the GPCRO activities will work without any problems as per the expectations or requirements.
×A quality control officer and the safety officer at GP CRO. Her Medical Technologist background work on molecular techniques associations with genetic disease and safety diagnostics. She started work at GPCRO in 2017 to perform bioanalysis. She continued to work with a further quality control officer supports quality in terms of field laboratory activities for ensuring quality control services as well as managing specimen logistics and archiving. She has also started working as a laboratory safety officer. Her responsibility is to assist the team in contributing to the improvement of the workplace, including laboratory processes and methods, laboratory safety, and the working environment in accordance with ISO 15190.
×Currently a Laboratory Supervisor at the GlobalPlus Diagnostics Laboratory at Bangkok, Thailand. He is Medical Research Technologist and has expertise in clinical research about tropical medicine and infectious disease, regenerative medicine and oncology. His interest in clinical research developed over the years since he had worked in clinical research of tropical medicine and infectious disease; malaria at International NGO, he decided that he wanted to pursue a career in Medical Research Technologist. He believed that further research and discoveries in the field could make a difference in the lives of many. Mr. Yingyuen had worked at Armed Forces Research Institute of Medical Sciences as Senior Medical Research Technologist more than 10 years before being appointed to his current post as Laboratory Supervisor at GlobalPlus Diagnostics Laboratory. During this time, he developed a lot of experimental and successful research-based approach to tropical disease. He worked together with a multi-disciplinary team of scientists and clinicians to develop new drug susceptibility assay for malaria research. During this time he built up his research and publication profile, both nationally and internationally. He also delivered substantial contributions in leadership, teaching and management. .
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