Case Study: Managing supply timelines for clinical trials

Customer need

• Clinical supplies for multiple-ascending dose study with six dosage groups and two groups of subjects
• Support for concurrent studies in multiple locations with flexibility requirements
• Speedy supply requirements to support commencement of clinical trials two weeks from manufacture
• Logistics support for retaining stability of drug during transport

What we did?

• Ensured quick packaging post manufacture through seamless integration between formulation and CTS
• Standardized packaging design for consistency across studies and ensuring maximum flexibility of supply
• Provided drug storage and transportation in cold chain environment using validated equipment and processes

Value to the customer

• Study medication delivered on time which enabled timely start of clinical trials
• Regulatory advice and support