Duration: 12 months

Campus: UK or Singapore (Commencing in late 2010 in Singapore)

This course aims to provide graduates with the practical knowledge and skills to describe, implement and manage the processes of drug development in an international environment required to achieve global regulatory approval for new pharmaceutical products. Additionally through a dissertation student passing the Post Graduate Diploma will be able to critically evaluate the said processes.

• Fundamentals of Drug Discovery, development and design of clinical trials- Simulation/role play & on-line ICH-GCP certification
• Global business and marketing strategies in Clinical Research- Simulation/role play
• Global Resource Management- Simulation/role play
• Global Data Management- Simulation/role play
• Global Product Registration, Pharmacovigilance and Post Marketing Surveillance-Pharmacovigilance role play exercise

• Global experience in Clinical Trails Management
• Work in a team and apply the tools and techniques of project management to scope and schedule clinical research projects and processes and to communicate the project outcomes orally and in writing
• Effectively communicate technical information in writing and in an oral presentation
• Act as a source of professional clinical research advice and expertise
• Practical exposure in simulator units
• Career advice, screening of CV by Reed Scientific

(MBBS/BDS/B. Pharma/BHMS/BAMS and their respective post graduates/Life Science graduates & professionals from relevant disciplines) IELTS:6.0

*Fees valid for March 2010 only
Balance fee should be paid before applying for visa.