• Creative Design for studies
• PRO Document licensing support minimizing acquisition timeline and compliance issues
• In-house clinical-centric Translation Management delivering IRB and EC compliant solutions
• Web-based collaborative proofing saving valuable time and expense lost to conventional proofing practices
• Investigator meeting materials and collateral support
• Logistics capable to support global footprint requirements for international studies
• Study Closure support and materials recovery solutions to improve depot recovery of residual items
• Real-time information management through the Imperial Marketplace which is tailored to the needs of global project mangers

Time is the new currency; clinical teams face a historic array of emerging challenges today, forcing many to re-evaluate the cost of working with suppliers who do not understand their needs.  Imperial is approaching 40 years of experience with maximizing site initiation.  After our clients collaborate with our Design Services on the creative process, we can support the rapidly changing requirements of their LTM’s and PM’s.  Our Translation team is experienced in well over one hundred languages and that number continues to grow.  They work with the unique IRB/EC requirements on a daily basis allowing us to minimize the timelines associated with revisions and disruptions.  Our Production & Fulfillment group boasts not only industry leading quality controls and efficiency due to our lean practices, but has also delivered final product to over 90 countries including over 72,000 shipments ex-U.S. in the last 3 years. 

Not only has the global requirement challenged clinical teams, but the requirements of eClinical support have continued to increase as well.  Imperial can accommodate and integrate needed eClincal services from study design to include training, reference, and educational support.  In addition, the EDC study closure requirement solutions offered by Imperial include logistics, archiving, user acceptance testing and audit support.