Improving your clinical trial design in Asia for enhanced trial quality, by Ms Patrecia Valone

In Clinical Trials by valerie limLeave a Comment

Discover how to improve your clinical trial design for enhanced trial quality from Ms Patreica Valone, Director, Development Operations, Takeda Global Research & Development Center, Singapore. She will be presenting at Pharma Trials World Asia 2012, part of a series of conferences at the 5th Annual BioPharma Asia Convention 2012.

Ms Valone has over 19 years of experience in Clinical Research across a variety of therapeutic areas. Ms Valone received her Bachelors' and Masters' degree in Nutrition from the University of Massachusetts, Amherst, MA, USA. She has worked in academics conducting neonatal studies before moving to Quintiles, one of the largest Contract Research Organizations (CRO) globally and most recently joined Takeda TGRD Asia managing all clinical programs in Asia. Ms Valone has worked in multiple roles in Clinical Operations and Quality Management.

She will be speaking about the following topics:

1. Formulating approaches for maintaining standard of care at Asian sites with high patient load
2. Maintaining control over trials with flexibility for CROs' input
3. Success case study: Engaging CROs for increased data quality and patient safety

Join us at BioPharma Asia Convention 2012 to gain valuable insights from more than 200 experts. Contact us now for more details!

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