Drug Development Digital Solutions
Your innovative partner in optimizing drug development and clinical research
Biotech and biopharmaceutical companies face significant challenges in drug development, including slow study startups, inefficient site selection, data management issues, lack of transparency, regulatory compliance hurdles, and operational inefficiencies. Drug Development Digital Solutions by Thermo Fisher Scientific are where our innovation meets your excellence. Designed to meet these challenges head-on, we are redesigning the entire clinical research model with purpose-built, CRO-owned technology integrated into every study. Our forward-thinking, AI-enabled solutions accelerate and optimize every phase of your clinical development journey.
Our digital ecosystem is more than just technology; it’s the foundation for conducting faster, higher-quality trials. Each digital solution we offer plays a vital role in achieving clinical excellence, creating a seamlessly integrated digital experience that sets new standards in drug development. We help biotech and biopharmaceutical companies achieve faster study startups, smarter site selection, cleaner data, increased transparency, streamlined regulatory compliance, and greater confidence across the board.
Drug development digital offerings
At Thermo Fisher Scientific, we understand the complexities and challenges you face in clinical development. That’s why we’ve developed a range of advanced digital solutions that leverage AI to provide you with clarity, confidence, and efficiency throughout your clinical trial journey.
Clinical Decision Suite
Gain clarity and confidence
An AI-driven approach offering a unique end-to-end view, providing real-time insights and integrating milestone monitoring, risk prediction, material management, and tracking. Built on the principles of security, efficiency, and risk mitigation, it enhances efficiency, reduces complexities, and ensures faster trial completion with high-quality results.
Clinical Trial Forecasting Suite
Accelerate your trial startup
A new AI-powered platform leverages deep learning models and proprietary data to enhance forecasting accuracy and optimize clinical trial planning. It predicts milestones, streamlines site selection, forecasts patient enrollment and anticipates delays. With continuous, adaptive learning, our algorithms remain accurate and current, offering real-time insights for proactive management and early risk mitigation.
Intelligent Clinical Suite
Achieve faster database lock
Our sophisticated AI significantly enhances the speed, quality, and resource efficiency of clinical trials. Intelligent clinical suite offers a comprehensive approach to study execution and data management, accelerating drug time-to-market through faster actions and more efficient planning. By fostering collaboration and bringing all study stakeholders together in a seamless, connected environment, our Intelligent Clinical Suite improves communication and decision-making under one technological “roof.”
StudyGage
Predict and enhance patient participation
Our innovative, proprietary study patient burden tool leverages over 60,000 patient study participation decisions from a diverse global sample. This transformative tool enhances traditional feasibility assessments by incorporating patient perspectives, leading to optimized study designs and improved enrollment outcomes. Seamlessly integrating into existing processes, this tool ensures more efficient and patient-centered clinical trials.
Drug development digital applications
There are many complexities you face when executing clinical trials. Our innovative software solutions are designed to streamline the process, ensuring you achieve clarity, confidence, and efficiency at every step.
PPD™ Patient First Digital Solutions Smart Screening
SMART pre-screening leverages AI to enhance referral quality by integrating effortless health record extraction for real-time access to medical histories. Advanced algorithms evaluate these records against the protocol’s inclusion/exclusion criteria, offering a “probability-to-enroll” rating. This innovation minimizes the time spent on patients who do not qualify, thereby improving the quality of referrals to sites.
PPD™ Patient First Digital Solutions Patient Recruitment and Engagement
Patient recruitment and engagement is at the core of our strategy, utilizing a patient-first, digitally-enabled approach to streamline the clinical trial process. By leveraging AI-powered tools and extensive data, we ensure precision in identifying and engaging the right participants globally. Our end-to-end recruitment platform maximizes enrollment efficiency and minimizes site burden, ultimately accelerating study timelines. This comprehensive approach transforms traditional recruitment methods, making the clinical trial journey easier and more accessible for patients.
PPD™ Risk Assessment & Mitigation Platform (PPD™ RAMP)
Risk Evaluation and Mitigation Strategies (REMS) are essential to the safe use of high-risk medications and technology plays a key role in streamlining these programs and improving outcomes. Our 21 CFR-compliant, cloud-based platform combines enhanced user functionality and a 360-degree view of the patient journey to drive efficiency, accuracy, and data security. Built to support complex, multi-sponsor REMS, PPD™ RAMP offers real-time visibility and rapid adaptability to evolving regulatory requirements—ensuring long-term program success.
TrialMed Site Operations Management Solutions (SOMS)
Our enterprise site intelligent trial suite, including CTMS, eSource, regulatory, patient payments, and site-to-patient engagement functions, offers a seamless study management tool. The TrialmedTM Site Operations Management solution is a comprehensive ‘one-stop shop’ supporting our global site network across all study phases, enabling full digital integration. It incorporates business-driven functionalities such as operational data model (ODM), site resource management, labs management, cardiovascular monitoring, pharmacy, sample management, recruitment management, and business intelligence reporting.
Leverage over 15 years of expertise in integrating clinical and lab data with Preclarus Lab Solutions.
Our proprietary web-based lab data management system offers project teams real-time access to data, enabling accurate and informed decision-making. It ensures reliable, integrated data, allowing you to make better decisions faster. The Preclarus™ central lab enterprise and information management system guarantees a swift and precise study startup. With its innovative laboratory data management software, it expertly manages every aspect of central lab clinical trials, ensuring efficiency and accuracy throughout the process.
Drug development digital frameworks
To provide the best service and results for our customers, we prioritize optimal efficiency in our operations. We continuously seek ways to enhance and refine our internal processes, enabling us to deliver exceptional quality and success to our customers.
The Modern Data Platform provides seamless access to high-quality, governed data, empowering informed decision-making and cultivating a dynamic, data-driven culture. The platform transcends traditional capabilities, offering a robust solution to optimize data operations, enable advanced analytics and enhance customer experiences, all while maintaining the highest standards of data governance, privacy and security.
Our proprietary generative AI tool helps colleagues boost their productivity and revolutionizes the way we work. This powerful tool transforms how we deliver value to both our colleagues and customers, enhancing efficiency and driving exceptional outcomes across the board. We maintain strict human-in-the-loop oversight of all our artificial intelligence tools to ensure the highest quality outputs.
