As the sole provider of end-to-end clinical trials process management services, Ancillare is ready to develop your protocol specifications into clinical success. Our global network, team of experts, infrastructure and technology enable us to fulfill requirements of protocols of all sizes and complexities. Whatever the size, our dynamic partnership can support your trials from start to finish with services including protocol analysis, clinical logistics, ancillary product and comparator sourcing, documentation management, regulatory compliance and clinical kitting and packaging. Ancillare works closely with clinical leads and investigator sites to build the clinical trial supply chain and support necessary to reduce time and costs, create efficiencies and accountability and mitigate risk at a global level.

Managing global clinical trials creates increasing complexities for clinical leaders today. Identifying site locations and building a supply chain robust enough to handle the scope of operations is a difficult task. Fluctuating global regulatory guidelines, local restrictions and authenticity concerns create challenges for planners. Lastly, demand analysis and process tracking at a global level provides uncertainty in the system. These difficulties create sources of protocol failure that can lead to delayed or cancelled clinical trials. Ancillare understands these challenges and works directly to mitigate protocol risk and provide support to clinical leaders throughout the world. From our unique staff augmentations that provide the expertise needed for success, to our global supply network needed to execute the protocol, we can help our partners achieve protocol success on time and on budget.

Our clinical trials process management services can eliminate protocol complexities and assist in every aspect of the clinical trial supply chain.

Our proven services include:

• Staff augmentation designed to provide clinical leads with the technical support and expertise necessary to manage the global clinical network. Our Ancillare Professional Teams (APTs) are therapeutic area based and centrally manage the protocol for process excellence
• Ancillary product sourcing and acquisition per protocol specifications
• Comparator product sourcing and acquisition
• Clinical logistics including global distribution, kitting, packaging, tracking, resupply, return and destroy management
• Quality assurance and storage including ambient, clean, cold and frozen conditions
• Documentation gathering and analysis for global regulatory compliance
• Protocol analysis, key performance indicators and records maintenance
• Proprietary software dashboard for clinical process
• Clinical services including encapsulation and blinding strategies, clinical packaging, labeling and translation services

Most importantly, our approach is completely customizable to fit your strategic goals, company and development requirements. Ancillare is your partner for clinical trials process management to reduce costs, build efficiency and manage complexity and risk at a global level.