QP Services Delivering Global Regulatory Requirements
With an unparalleled regulatory history, we provide QP Services through our team of Qualified Persons (QPs) who play a vital role in bringing your new products to market. Our highly experienced team ensures that clinical studies not only meet the most vigorous standards but also run smoothly, seamlessly and cost- efficiently. Our team of qualified persons assume responsibility for all stages of the process, safeguarding patients including the audit of the supply chain for GMP compliance in addition to certification of products for use in clinical trials. At PCI, our QPs also offer a consultancy service to ensure that operations are in-line with all relevant EU directives and other necessary regulations.
Our consultative and flexible approach combined with expertise ensures optimization of clinical trial costs and efficiencies.
• Dedicated Project Management
• pci | bridge TM
• Interactive Response Technologies (IRT)
• Comparator Sourcing
• Distribution and Logistics Planning
• Language Translation
• Multi-language Labeling
• Randomization
Together, delivering life changing therapies.
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