Beyond startup, acceleration
across the entire trial lifecycle
AcceleROUTE™: Efficiency Strand
From initial feasibility to final study closure, we use AcceleROUTE™ Efficiency Strand to streamline processes, proactively identify risks, and ensure adaptability-so your study maintains momentum and achieves success.
Streamlining your clinical trial journey
Accelerate your research, not just your startup. AcceleROUTE™ is our Efficiency Strand, designed to optimize every phase of your clinical trial, from feasibility to closure. We ensure speed, quality, and budget control remain paramount throughout the entire process.
Four integrated streams for seamless execution
Unlike CROs that focus solely on startup, AcceleROUTE™ integrates four critical phases into a comprehensive approach. It begins with Study Oversight and Management, ensuring administrative integrity and compliance through streamlined processes and proactive risk mitigation. This is followed by Startup Acceleration, which rapidly activates sites by efficiently allocating resources, negotiating contracts, and managing vendors. The next phase, Study Conduct Optimization, maintains trial momentum through proactive monitoring, data quality oversight, and adaptable solutions. Finally, Efficient Study Closure is achieved by planning for timely database lock and reporting while managing data integrity.
1. Study Oversight & Management: Efficient execution, empowered by expertise
Streamline your clinical trial operations without sacrificing quality or control. Our Study Oversight & Management team provides expert administrative support, ensuring seamless execution and adherence to protocols.
• Experienced oversight: Our dedicated team brings extensive knowledge and experience, proactively managing trial logistics and ensuring compliance.
• Cost-effective solutions: We provide access to well-trained resources at the execution level, optimizing your budget without compromising quality.
• Agile & responsive support: Adapting to your study's evolving needs, ensuring efficient communication and timely issue resolution.
With Accelsiors, you gain a trusted partner dedicated to maximizing your trial's efficiency and agility, allowing you to focus on achieving your scientific goals.
• Experienced oversight: Our dedicated team brings extensive knowledge and experience, proactively managing trial logistics and ensuring compliance.
• Cost-effective solutions: We provide access to well-trained resources at the execution level, optimizing your budget without compromising quality.
• Agile & responsive support: Adapting to your study's evolving needs, ensuring efficient communication and timely issue resolution.
With Accelsiors, you gain a trusted partner dedicated to maximizing your trial's efficiency and agility, allowing you to focus on achieving your scientific goals.
2. Startup Acceleration: Rapid clinical trial site activation, on-time enrollment
Time is of the essence in clinical trials. Our Startup Acceleration team expedites site activation, enabling swift patient enrollment and minimizing costly delays.
• Efficient site selection and contracting: Utilizing our extensive network and expertise to identify and onboard the most suitable sites quickly.
• Streamlined regulatory and ethics submissions: Preparing and managing submissions, ensuring compliance and minimizing approval timelines.
• Optimized resource allocation: We strategically deploy resources to ensure your trial is fully operational and ready to enroll patients as soon as possible.
With Accelsiors, you can launch your trial with confidence, knowing that every step is optimized for speed and efficiency.
• Efficient site selection and contracting: Utilizing our extensive network and expertise to identify and onboard the most suitable sites quickly.
• Streamlined regulatory and ethics submissions: Preparing and managing submissions, ensuring compliance and minimizing approval timelines.
• Optimized resource allocation: We strategically deploy resources to ensure your trial is fully operational and ready to enroll patients as soon as possible.
With Accelsiors, you can launch your trial with confidence, knowing that every step is optimized for speed and efficiency.
3. Startup Stream: Accelerating site activation, minimizing delays
Delayed site activation can impact your trial timeline and budget. Our Startup Stream team proactively tackles this challenge, streamlining essential tasks from document management to vendor alignment.
• Efficient document handling: Coordinating document collection, reviewing, and submission, ensuring compliance and minimizing approval delays.
• Expert contract negotiation: Our deep understanding of local legal and regulatory requirements ensures smooth site contract execution, avoiding costly setbacks.
• Seamless vendor alignment: We expertly manage vendor selection, qualification, and onboarding, including study-specific training, guaranteeing a smooth study start.
With dedicated leadership, advanced technologies, and a cross-functional team, our Startup Stream gets your trial up and running swiftly, keeping you on track for success.
• Efficient document handling: Coordinating document collection, reviewing, and submission, ensuring compliance and minimizing approval delays.
• Expert contract negotiation: Our deep understanding of local legal and regulatory requirements ensures smooth site contract execution, avoiding costly setbacks.
• Seamless vendor alignment: We expertly manage vendor selection, qualification, and onboarding, including study-specific training, guaranteeing a smooth study start.
With dedicated leadership, advanced technologies, and a cross-functional team, our Startup Stream gets your trial up and running swiftly, keeping you on track for success.
4. The Study Closure Stream: Seamless database lock, confident results
Achieving a timely and accurate database lock is critical for your clinical trial's success. At Accelsiors, we prioritize this milestone from the very beginning. Our Study Closure Stream team, guided by project and data management experts, proactively ensures data integrity throughout your trial.
• Early preparation: We implement a Quality by Design (QbD) approach, meticulously setting up your study for seamless closure from day one.
• Ongoing oversight: Our dedicated team actively monitors data quality, facilitating timely and efficient database lock.
• Confident results: Experience reduced stress, minimized delays, and complete confidence in your trial data, enabling swift analysis and reporting.
With Accelsiors, database lock is a planned achievement, not a last-minute scramble.
• Early preparation: We implement a Quality by Design (QbD) approach, meticulously setting up your study for seamless closure from day one.
• Ongoing oversight: Our dedicated team actively monitors data quality, facilitating timely and efficient database lock.
• Confident results: Experience reduced stress, minimized delays, and complete confidence in your trial data, enabling swift analysis and reporting.
With Accelsiors, database lock is a planned achievement, not a last-minute scramble.
ProPATIENT Solutions™
The colision of information provided to us by both patients and care givers is what makes our approach unique. Patients are central to our approach, which allows us to better both their experience and your trial outcomes significantly. That is why we like to refer to ProPATIENT Solutions™ as our first-hand tool.
