“GreenLight Clinical is passionate in their pursuit of ingenious services that save time and money for their clients and heroic in their ambitions to ensure the health and safety of patients. GreenLight Clinical strives to be a trusted partner in creating a world of safer drugs”
It is a great pleasure to welcome you to GreenLight Clinical where we are taking research beyond results.
With a focus on the highest quality data, the highest standards of safety, and the most advanced technology the market has to offer, GreenLight Clinical delivers truly unique clinical research services that are being rapidly embraced by a growing list of pharmaceutical partners from around the world.
We employ the skills of many clinical research professionals exclusively focused on providing professional, high quality study conduct and drug development services. We are actively involved in both government, industry-sponsored investigator-initiated and commercial trials translate to in more than 15 therapeutic areas. Trials ranging from proof of concept trials to phase IV, evidence-based medicine and epidemiology studies.
GreenLight Clinical offers a very broad range of clinical services that are intended to help our clients complete clinical trials as quickly and efficiently as possible, as well as ensure that appropriately high standards and levels of quality control are maintained from beginning to end.
Clinical research is the key driver of critical factors for new advancements in medicine today. It is therefore, vital to continue developing healthcare practices through clinical research. GreenLight Clinical is proud to be the collaboration partners of many of these clinical research projects.
Dr Sasi Suda
CEO, GreenLight Clinical
Dr Sasi Suda initially qualified as a medical doctor in Thailand and Australia, she spent her Residency in large University hospitals in Bangkok and Japan, practicing across a number of disciplines including oncology, neurology, chronic pain, cardiology and general medicine.
In combining her clinical experience and research training, Dr Suda has subsequently worked in several pharmaceutical, biotechnology and medical industries in Australia, holding key executive and clinical management roles at various global pharmaceutical companies. With over 15 years experience in international clinical project management and medical affairs, Dr Suda has worked across a range of therapeutic areas – notably in ophthalmology, immunology and oncology – and on significant disease conditions including multiple sclerosis, HIV/AIDS and diabetes. She has specific expertise in clinical operations planning, investigator recruitment and liaison, site selection and setup, clinical outsourcing, contract negotiation, drug safety management, regulatory submissions, and clinical research training.