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CRITICAL PATH CLINICAL SOLUTIONS

                                                                             FULL SERVICE CLINICAL RESEARCH ORGANIZATION OF TOMORROW...TODAY

CLINICAL INNOVATION AND EXCELLENCE
CRITICAL PATH CLINICAL TRIALS CRO

AGILITY    FLEXIBILITY    EXPERTISE

INNOVATIVE CLINICAL RESEARCH ORGANIZATION

Critical Path Clinical delivers innovative, customized drug development planning and delivery. From trial design and feasibility to site selection, project management, and data analysis, our skilled team of experts ensure your trial stays on a successful path. Our integrated team manages all aspects, including monitoring, biostatistics, and report writing.

Collaborative, communicative, transparent relationship building are at the helm to ensure accelerated trial management. At the onset, we develop a collaborative team portal, keeping you informed with data analytics, meetings, status reports, and prompt responses. Custom data analysis strategies are tailored to your trial, guiding decision-making and clinical development. Our expertise allows for proactive, risk planning and identification and the flexibility to pivot rapidly and adjust plans to maximize your program's success.

Our expansive network of partnerships and resources allow for rapid site activation through centralization of trial assets, a customized work breakdown structure, plans and digital assets.  

Our Approach to Optimizing Clinical Operations

Critical Path Clinical Connect is driven by forward thinking innovations aimed to accelerate quality, safe trial delivery for patients through a pioneering platform that serves as a Clinical Trial in a Box. The pioneering platform integrates all stakeholders and functional roles into a clinical trial phase driven approach providing a birds eye view of the E2E Clinical Trial Lifecyle.

 

We specialize in identifying and implementing cutting-edge solutions to streamline operational workflows and maximize efficiency across clinical trial processes. Our expertise spans the design, development, and optimization of clinical trial management systems (CTMS), ensuring seamless integration with your existing platforms. We enhance data collection and analysis methods to provide actionable insights, ensuring precision and compliance at every step.

CUTTING EDGE CLINICAL DEVELOPMENT

Critical Path Clinical Connect is driven by forward thinking innovations aimed to accelerate quality, safe trial delivery for patients through a pioneering platform that serves as a Clinical Trial in a Box. The pioneering platform integrates all stakeholders and functional roles into a clinical trial phase driven approach providing a birds eye view of the E2E Clinical Trial Lifecyle

FUNCTIONAL ROLE ALIGNMENT
The E2E Work Breakdown Structure is fully functional allowing for  guided clinical trial delivery  using a digital platform integration approach. CPCC is designed to be user-friendly and accessible to all stakeholders involved in the trial, including researchers, clinicians, regulatory authorities, and patients.
 
AI ENHANCED
CPCC is integrated into an AI powered, digital platform, which allows the live embeds of regulatory guidelines to update along with the source requiring little maintenance. The digital platform is hosted on a secure server with appropriate firewalls and encryption measures to ensure the security of the data
 
COMPLIANCE
The immersive, digital E2E lifecycle solution is developed using a foundation of regulatory guidelines that cover the entire lifecycle of a clinical trial, from concept, initiation to completion and submission. Information on each stage of the clinical trial process, including patient activities, regulatory compliance, and best practices are embedded for live sources including regulatory guidance.

  1. COMMUNICATION

  2. CPCC includes clear instructions and guidelines for effective communication and coordination between all stakeholders involved in the trial. This helps to minimize inefficiencies and miscommunications, thereby enhancing the overall success of the trial. This is accomplished through the framework PPM platform which allows for messaging and chat within.

  1. STAKEHOLDER ENGAGEMENT
  2. Critical Path Clinical Connect serves as a platform with multiple channels and  segments allowing for internal and external vendor collaboration.
  1. MICROSOFT INTERGRATION
  2. CPCC can be fully integrated with Microsoft increasing efficiency through Outlook, Teams and other products to allow for emailing from within the platform, sending emails to the platform and full use within teams.

We specialize in identifying and implementing cutting-edge solutions to streamline operational workflows and maximize efficiency across clinical trial processes. Our expertise spans the design, development, and optimization of clinical trial management systems (CTMS), ensuring seamless integration with your existing platforms. We enhance data collection and analysis methods to provide actionable insights, ensuring precision and compliance at every step. Additionally, we offer tailored risk-based monitoring strategies, enabling proactive management of potential risks and ensuring trials are conducted with the highest standards of quality and oversight.

As digital data standards increasingly become regulatory requirements, it's essential for your organization to be ready. Although this may seem like a significant challenge, our dedication to excellence ensures a proactive approach. We’ve rigorously assessed, tested, and developed multiple prototypes, offering the flexibility to customize solutions tailored to your needs. Prioritizing People and Patients.

Creating exceptional patient-centric clinical trial experiences requires a holistic approach that prioritizes the needs and perspectives of patients at every stage. By engaging patients as partners, designing flexible and inclusive trials, improving logistics and support, adhering to ethical standards, and continuously seeking feedback, researchers can enhance patient satisfaction and improve the overall success of clinical trials. Embracing patient-centricity not only benefits participants but also contributes to more robust and reliable research outcomes, ultimately advancing medical science and patient care.

PATIENT TRANSPARENCY

Patients lack access to community support and trial centricity whereas there is limited transparency on the overall clinical trial ecosystem, which may decrease the likelihood of participation. In addition, the current format of informed consents lack consideration for diversity in terms of cultural, learning styles and delivery. Difficulty engaging and retaining patients, which directly impacts trial outcomes.

ENAGEMENT

CPCC also considers the unique needs and activities of patients, providing guidance on how to involve and retain patients in the trial. This includes providing clear instructions on how to obtain informed consent, how to communicate with patients about the trial, and how to ensure patient privacy and confidentiality.

PATIENT CONCIERGE PORTAL

CPCC also considers the unique needs and activities of patients, providing guidance on how to involve and retain patients in the trial. This is crucial for the successful completion of the trial, as patient participation and retention can significantly impact the outcome. The interface comes with the capability to have an investigator site portal and patient communication portal available on the web and app.

PATIENT CENTRIC CLINICAL TRIAL EXPERIENCE
Patient-centricity in clinical trials involves designing and conducting research in a way that is responsive to the needs and values of patients. It is about engaging patients as active partners rather than passive subjects. This approach can lead to higher recruitment and retention rates, better data quality, and more meaningful outcomes. By focusing on the patient experience, trials can become more efficient, ethical, and successful in generating reliable data. 

ENGAGEMENT
Careful coordination and communication for clinical development is critical to ensuring the quality, efficient and successful delivery of clinical trial and there is often a gap in access to sites and site access to CROs or trial Sponsors.


TRAINING AND SUPPORT
Training and coaching programs are developed to support the implementation of CPCC. These programs are designed to equip all stakeholders involved in the trial with the knowledge and skills needed to effectively participate in the trial process. 


PATIENT EXPERIENCE
Collect feedback from participants about their trial experience and use it to make real-time adjustments and improvements.
Foster a culture of continuous learning and improvement within the trial team by regularly revieing patient feedback and incorporating lessons learned into future trials.

Effective clinical trial budget management requires proactive strategies to prevent cost overruns and the "leaky pipe" effect. By leveraging robust forecasting, cost control, and change management techniques, our experts ensure financial accuracy and operational efficiency. Engaging our team early in the process lays a solid foundation for streamlined project delivery, guaranteeing both quality and speed in achieving your trial milestones.

Our consulting services provide comprehensive market insights and intelligence tailored to the life sciences sector. We analyze key industry trends, competitive landscapes, regulatory shifts, and emerging opportunities to deliver actionable intelligence. This enables biotech, pharmaceutical, and healthcare organizations to make informed strategic decisions, optimize their market positioning, and stay ahead in a rapidly evolving industry. With deep expertise and a data-driven approach, we help you navigate complex market dynamics and unlock growth potential.

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Our Approach to Optimizing Clinical Operations

CLINICAL TRIALTREK HOME 1

Tailored Patient Engagement

Master Service Agreement - Budget Management

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OUR PARTNERS

 

Partnering for Excellence in Clinical Research

Our organization emphasizes quality and knowledge, leveraging a global network of over 300 solution partners. Together, we innovate and implement best practices in clinical trials, ensuring that our collaborative efforts lead to groundbreaking discoveries and enhanced patient outcomes. Join us in shaping the future of clinical research through excellence and partnership.

PASSION FOR MAKING A DIFFERENCE

Passion for Making a Difference
At Critical Path Clinical, our passion lies in making a meaningful impact on the lives of patients worldwide. Partnering with us means entrusting your clinical research program to experienced professionals dedicated to helping you achieve your goals. We are committed to accelerating your clinical development program and bringing innovative therapies to market faster.

Get in Touch
Are you ready to revolutionize your clinical research program? Contact Critical Path Clinical today to discover how we can support your journey and help you bring life-saving therapies to market with unmatched efficiency and effectiveness.

By choosing Critical Path Clinical, you're opting for a partner that combines expertise, innovation, and a commitment to quality, ensuring your clinical research program's success every step of the way.