Establishing Minerva Research Solutions has allowed us to conduct clinical trials to find solutions for a wide range of chronic and life-threatening diseases. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Services as Solutions
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.
— Optimizing & Delivering Quality
Clinical Data Management & Operations
Minerva Research Solutions is one of the leading clinical support providers. We provide services including efficient and authentic clinical data management and data operations with the assistance of our competent workforce.
Minerva Research Solutions aims to transform the health information system by incorporating cutting-edge technologies in clinical data management and data operations. To cater to the needs of data operations we have a robust quality assurance team — accountable for delivering clean and precise data to minimize the chances of error and ensure quality data.
— Revolutionizing & Delivering Real-world Insights
The success of clinical services is significantly influenced by patient recruitment. Minerva Research Solutions’ direct-to-patient recruitment helps remove barriers that extend recruitment efforts’ time, cost, and uncertainty by utilizing machine learning and patient data and insight.
With the help of hyper-targeted outreach campaigns, Minerva can locate both directly identified participants and site-based patients outside of the site’s known population. We make this happen through our precise clinical data management capabilities and study-specific engagement strategy.
— Transforming Compliance & Accelerating Study Startup
Our regulatory teams are qualified and equipped to provide regulatory consulting and product lifecycle management services ranging from early clinical development to clinical data submissions and marketing authorizations. We provide compliance and real-time risk reduction in study startups by connecting our expertise, technology, and real-time insights. Our regulatory intelligence, data-driven methodology, as well as unparalleled attention to detail, establishes us as leaders in clinical services.
Our regulatory teams assist with the preparation of all major regulatory dossiers, including complex submissions, and clinical trial support services for regulatory. Our regulatory project management oversight includes a quality control review of each document and clinical data management.
Our clinical trial support services include patient recruitment and retention, clinical data management, and site selection services to make sure that quality data and the right kind of information are gathered cost-effectively.
At Minerva Research Solutions, we focus on the big picture and strategize for your specific needs. We work on any software system that brings us success. We don’t offer a single, universally applicable solution. We are available to offer the best representation during your trial in all aspects. However, to fulfill your study requirements, we do use Real-Time CTMS and the sponsor’s or CRO’s respective EDCs to ensure the integrity of the scientific data being collected.
Yes, we do have a medical affairs advisory group that provides quality compliance and regulatory consulting services to deliver guidance with respect to legal and regulatory operations.