Implement improvements in existing integrated cold chain. Improvements are usually identified in the assessments above or can be driven by customer-identified work. This work includes qualification of technology, writing of Standard Operating Procedures, management /execution of testing as required, writing of technical documentation in support of SOPs or testing.
Perform an audit of an organization (usually a pharma/biotech company) versus current Good Distribution Practices in the biopharma industry. Prepare a report with observations, root cause failure analysis, and mitigation strategies for the observations.