Our Main Drivers to Accelerate Clinical Drug Development

StrongCORE Scientific contribution

Scientific approach – StrongCORE SCIENTIFIC™

Maximize the value of your clinical development program with our flexible, fit-for-purpose consulting solution called StrongCore Scientific (SCS) and gain access to a multidisciplinary team of experts which is always uniquely composed; team members are selected and involved in harmony with the special development needs.


We not only monitor a study! We provide you with our specialized scientific and medical experts who have practical, in-depth knowledge of the therapeutic area to plan and lead your study, who understand your needs, interpret data in its real context, tailor the clinical development strategy and advise you concerning the optimal strategic direction at any stage of the study. The SCS team consists of Accelsiors’ subject specialists and consultants from various professional fields. This team has significant experience in all phases of clinical development and expertise across the entire pharma and CRO industry with an advanced educational and professional background in life sciences.

This experienced, science-driven staff can clear the way to proceed your study in a time and cost efficient manner by understanding the science, preparing innovative development plans and strategies, evaluating study designs and eliminating roadblocks on the path of your clinical trial.

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Quick patient access – ACCELEROUTE™

Acceleroute™ is our site pre-classification and motivation program, developed for boosting the number of well-performing study sites, minimizing risk in site selection and significantly shortening the duration of patient recruitment. A new, accelerated way in study site selection.


Shorten timelines and minimize your risk in site selection! The most significant cost generator in a study is the duration of patient recruitment and maintenance of inefficient sites. Once your Request For Proposal is received, we immediately start to identify the top performing and most cost-effective sites from our global network in harmony with your defined core expectations. Following this robust, initial and proprietary feasibility classification, Accelsiors is able to offer a precise proposal for the site portfolio that will deliver the planned number of patients within an optimized cost and time frame.

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fine-tuned processes

High standards in project methodology – PACE™

Accelsiors provides predictable and assured handling of complexity and realizes your needs through all steps of the study with consistent processes, transparent performance metrics and proactive risk management with a strong focus on on-time, on budget project execution.


PACE™ is our standardized four-phase methodology guided by Accelsiors Project Managers to measure and track discrete, objective variables that are vital to the success of a clinical study. Accelsiors’ project management methodology is based on our almost two decades of expertise in conducting clinical studies managed by skilled project managers through design to execution and beyond.

Our core competence for successful project delivery is through a proactive, standardized and modular approach to study planning, process optimization, task- and timeline synchronization, improvements in cycle times, risk management and metrics-driven operational oversight. Our efficient approach provides a more predictable process to improve data quality, accelerate database lock and establish an early foundation for study closeout activities and deliverables, assuring you quality results within the expected timelines and budget.

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Risk based, preventive Quality Assurance

Risked-based approach with preventive Quality Assurance – QUALITY HEALTH CHECK™

At Accelsiors we have quality built-in to all of our processes and this quality centered approach is integrated into all of our clinical and business practices. Your clinical trial will be constantly monitored using performance, quality, risk and financial lead indicators.

Accelsiors’ study team processes live study data, manages and monitors data quality to resolve issues immediately and to proactively manage any project risks. Momentum builds with patient recruitment, patient monitoring and the active involvement of all team members with the objective of screening, enrolling, and retaining subjects who are, and remain, in compliance with the protocol. Queries that could affect future analysis and study closeout are raised and resolved immediately. With reliable data in hand, this approach paves the way for refinements that will ensure the successful analysis and reporting of the study.

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state-of-the-art clinical research technology

Integrated clinical trial technology – WIDESCOPE INTELLIGENCE™

We support our services with state-of-the-art integrated technology in all aspects of clinical research, ensuring access to Sponsor at every stage of our work processes providing a real-time hands-on experience about how your study is moving towards execution, within the expected timelines and budget, as planned and offered.


Once the study is underway, we will advance our proactive project monitoring system supported by state-of-the-art clinical trial technologies and standardized project dashboards. Your clinical trial will be constantly monitored by performance, quality, risk and financial lead indicators. When the first enrolled patient completes the study, our study team begins to review data and makes detailed plans to identify trends and address data issues focusing on resolving issues that could affect the analysis and study closeout. The team processes live study data, manages and monitors data quality to resolve issues immediately and to proactively manage any project risks and assuring you quality results within the expected timelines and budget.

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Our Mission

Mission statement

Accelsiors delivers strategic solutions for conducting global clinical trials with the ultimate objective of improving public health. We stand for acceleration, excellence and outstanding achievement in clinical drug development and we dedicate ourselves to serving the needs of our customers with:

Talented and experienced staff

Advanced data science

Therapeutic expertise

Comprehensive services

Global regulatory expertise

A personal touch, supportive culture

Flexible capabilities

Global reach

Accelsiors operates on a global scale utilizing local expertise to deliver the most reliable study results within the agreed budget and timelines.   Learn more!

Comprehensive Clinical Development Services

We are the only resource you need in the field of clinical trials, from study protocol design to product approval and anything in between. Learn more!