Our Services
An established leader in the field of clinical research, MedTrials offers a full spectrum of professional services including clinical trial management, monitoring, data management, biostatistical analysis and reporting in all phases and types of clinical trials.
MedTrials compliance experts conduct GxP audits at investigational sites, sponsors, manufacturers, IRBs and other third-party vendors. MedTrials trainers are well known for delivering dynamic and innovative presentations and programs throughout the world.
Our team's organizational and communication skills, responsiveness with both the sponsor and the investigative site, and relationship management are primary discriminating factors between MedTrials and other CROs.
It is these values and characteristics that allow MedTrials to deliver high-quality solutions through every step of the clinical research process. When you select MedTrials as your clinical research partner, you can expect to receive the highest level of professionalism and quality.
Clinical Trial Management
MedTrials has a strong reputation as Clinical Trial Management experts. Our teams are qualified by training and experience with the required knowledge, skills, and abilities to successfully deliver reliable data from protected subjects on time and within budget.
Our Clinical Trial Management services provide you with:
- Effective site management with accelerated study start-up and risk-based approaches.
- A broad range of experience across therapeutic areas of all phases and product types, in adult and pediatric populations.
- Integrated technology solutions for sponsor advantage.
- Reliability and expertise—we don’t just say we can do it; we have a proven track record.
- High-quality service and a values-driven company with a focus on customer satisfaction.
Informatics
MedTrials Informatics Team integrates a skilled team of professionals into the project development process as early as possible. This approach builds team identity and communication and promotes early collaboration in order to provide high-quality data that is accurate, accessible, and ready for analysis in a cost-effective and timely manner.
Our Informatics Team delivers:
- Customized data management solutions to satisfy client, regulatory, and scientific needs.
- Expertise in database development and data management activities using tools that best meet sponsor requirements.
- Assigned staff trained in therapeutic areas and study-specific assessments.
- Integrated technology solutions—automation and access to information to our study sponsor’s advantage.
QA & Compliance
MedTrials GCP quality experts provide support, consultation, and oversight as needed to verify the integrity of data and ensure the proper adherence to protocols. Clinical Quality Assurance (CQA) consultants also serve as virtual team members when contracted to fill open positions or to be available on retainer as needed.
Our QA & Compliance services include:
- CQA and GCP Compliance Support
- Quality System Consulting and SOP Development
- Clinical Quality Audits
- Vendor/Service Provider Qualification and Audits
- Quality System Audits
- Quality Investigations and Root Cause Analyses
- CAPA Planning and Oversight
- Gap Analyses
- Mock Inspections
Training & Professional Development
MedTrials delivers best-in-class, innovative, and impactful training in a variety of modalities—from live presentations to self-paced eLearning and simulations. Beyond just theory, our convenient, dynamic, and engaging presentations and training courses furnish you with a practical, real-world understanding of current issues and trends.
As an approved Continuing Education Provider through the State of Florida Board of Registered Nurses, MedTrials can offer CNE.
Most In-Demand Courses:
- GCP Training
- Annual GCP Update
- Industry Hot Topics
- Inspection Readiness
- Role-Based Training
- Project-Specific Training