CLINICAL RESEARCH & DEVELOPMENT SOLUTIONS
Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision-making, innovation with reduced risk, and driving trials without compromise so you can deliver life-changing therapies faster.
Clinical Research Services
BioFicher Sciences offers a robust suite of clinical research services for your Phase I-IV clinical trials, registries, and other clinical research Phase I-IV initiatives.
From complex protocols to added pressures to move faster, today’s clinical trial leaders face unprecedented challenges. With the power of BioFicher Connected Intelligence, we connect data, technology, analytics and trial expertise to help solve your biggest hurdles.
Development Plan
Bring real-world and commercial insights into your clinical development planning. Discover alternative paths and study designs that shorten timelines, decrease costs, and maximize your asset value.
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CLINICAL DEVELOPMENT STRATEGY
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CLINICAL TRIAL DESIGN
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R&D MANAGEMENT CONSULTING
Phase I
BioFicher is with you from the start, with expertise in complex early clinical studies, a global network of highly qualified Phase I units, and innovative data-driven approaches to accelerate proof of concept.
Reed Moore
Phase II & III
You can trust BioFicher to deliver your Phase II-III trials with quality, speed and efficiency. With experts across a complete range of clinical trial services and trial experience in 100+ countries, we can help you achieve your study’s goals.
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PHASE IIB/III DELIVERY
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PROTOCOL VALIDATION
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CLINICAL MONITORING
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GLOBAL LABORATORIES
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PATIENT RECRUITMENT
Regulatory Submission
Tap into BioFicher’s extensive regulatory expertise to confidently interact with regulatory authorities around the world. Our team of medical writers, biostatisticians, regulatory specialists and subject matter experts work together to deliver faster, more efficient submissions with the quality you need.
Reed Moore
Post-Marketing Studies
Regulatory authorities are now increasing opportunities for you to provide real-world evidence of your products’ safety and effectiveness. This changing environment can make your products more available to patients.
Reed Moore
Medical Writing
Regulatory authorities are now increasing opportunities for you to provide real-world evidence of your products’ safety and effectiveness. This changing environment can make your products more available to patients.
Reed Moore
Decentralized Trials
From complex protocols to added pressures to move faster, today’s clinical trial leaders face unprecedented challenges. With the power of BioFicher Connected Intelligence, we connect data, technology, analytics and trial expertise to help solve your biggest hurdles.
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CLINICAL DEVELOPMENT STRATEGY
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CLINICAL TRIAL DESIGN
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R&D MANAGEMENT CONSULTING
Patient Recruitment
Scalable and proven, decentralized trial solutions engage the right patients wherever they are. Our hybrid and fully virtual models have been fine-tuned in over 500 decentralized trials, across 30+ therapy areas, in more than 75 countries.
Reed Moore
Connected Device
Tap into BioFicher’s extensive regulatory expertise to confidently interact with regulatory authorities around the world. Our team of medical writers, biostatisticians, regulatory specialists, and subject matter experts work together to deliver faster, more efficient submissions with the quality you need.
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PHASE IIB/III DELIVERY
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PROTOCOL VALIDATION
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CLINICAL MONITORING
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GLOBAL LABORATORIES
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PATIENT RECRUITMENT
BioFicher Decentralized Trials
From complex protocols to added pressures to move faster, today’s clinical trial leaders face unprecedented challenges. With the power of BioFicher Connected Intelligence, we connect data, technology, analytics and trial expertise to help solve your biggest hurdles.
Translate science into new treatments
Through our Therapeutic Centers of Excellence, BioFicher connects your clinical program with strong scientific and medical expertise, deep therapeutic insights and unrivaled clinical trial experience to help you find the most direct route from breakthrough science to new therapies for patients.
Transformation with speed
By leveraging our extensive real-world data and predictive modeling, we can quickly predict the sites to deliver higher enrollment rates
Accelerating Timeline
46% FASTER
Clinical Trial Site Identification
