Maggie Lim | Clinical Development Quality Assurance (Asia-Pacific), Global Quality & Compliance
GSK Pte Ltd | Singapore

Maggie Lim, Clinical Development Quality Assurance (Asia-Pacific), Global Quality & Compliance, GSK Pte Ltd

With more than 18 years of experience in clinical research & operations, Maggie has spent most of her time in R&D early phase clinical development, led regional training for 5 years  before moving onto Clinical Development Quality Assurance within GSK R&D for the last  4 years. She has current specific responsibility for the quality of clinical studies audited within Asia Pacific and with the help of a team of audit advisors in the region, supporting and building  the quality of late stage clinical research development,  working strategically with the various clinical functions in AP countries, providing support in clinical research activity and also providing GCP advice and consultancy.

Appearances:



Phar-East pre-conference day @ 14:00

CLINICAL TRIAL AND ISSUES MANAGEMENT – SKILLS FOR EFFECTIVE SOLUTIONS

Project management skill is crucial in large scale, cross country studies. Whether you are from a sponsor company, or a CRO operating in Asia, it is essential learning from experts on skills for effective problem identification and solving. Coming from both provider and industry perspective Maggie Lim, Director, Clinical Quality Assurance of Pharma R&D, Asia-Pacific of GSK will share her 17 years’ experience in clinical research and trials management with you at this 2.5 hours workshop.Key topics to be covered in this workshop include:
  • Identifying root causes (Root Cause Analysis (RCA))
  • workout of Corrective & Preventive Measures (CAPA)
  • Measuring their effectiveness
last published: 26/Sep/18 02:35 GMT

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