Contract Research Organization
Aligning the Art & Science of Clinical Research®
Services Overview
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
Therapeutic Specialties
Ophthalmology
Working with ophthalmologists and their technical staff requires a special kind of CRO—MedTrials is that CRO. Since the mid-1990s, we have specialized in the monitoring and trial management of ophthalmology trials.
MedTrials staff have been repeatedly requested due to their specific understanding of ophthalmology trial management and data monitoring. Our extensive work in the field of ophthalmology means that we know the technical assessments and data requirements, and we "speak ophthalmology."
Dermatology
Dermatology drug development is filled with many unique challenges, such as the need to minimize diagnostic subjectivity in order to increase clinical and regulatory confidence in a trial’s findings.
Our clinical research services provide you with a body of experienced and dedicated professionals well-versed in that, and more.
From the intense monitoring of data in dose escalation trials to cost-saving approaches, such as targeted data monitoring, our experts know how to enhance the quality and timeliness of your particular dermatology trial results.
Cardiology
Experience has taught us that successful trial management begins with a thorough understanding of the science behind the process, including knowledge of this crucial therapeutic area.
MedTrials has vast cardiology experience, including supporting trials for catheters, stents, vascular closure devices, multi-use scalpels, and syringes.
Our MedTrials experts and project leaders serve as valuable consultants regarding project planning and oversight.
Gastroenterology
At MedTrials, we know that engaging the right people and the right processes are essential to providing exceptional service. Our project team members are well trained and have the resources and site relationships needed to move quickly and get the program started with efficiency.
With over 30 years of experience, MedTrials has the expertise necessary to plan and implement Phase I-IV programs for gastroenterology trials in a wide range of indications.
What Product Types Does MedTrials Have Experience In?
Medical Device
Pharmaceutical
BiotechnologyWho Can MedTrials Help?
Sponsors
Sponsors of pharmaceutical, biotech and medical device clinical trials can rely on MedTrials to deliver reliable data from protected subjects on time and on budget.
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Investigators
Clinical investigators who are responsible for conducting clinical trials can rely on MedTrials to help them navigate through heavily-regulated research requirements.
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Study Participants
Interested in participating in a clinical trial? Individuals who volunteer to participate in clinical trials are the most important part of the research enterprise.
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