Global Clinical Trial Consultants, LLC
Training on the following Topics:
HIPAA/Patient Privacy Laws
Monitoring
Study Coordinator Responsibilities
Clinical Investigator Responsibilities
Clinical Research Consultation
Any Organization, including Sponsors:
Clinical Investigators
Contract Research Organizations (CROs)
Customized Classes
Training for Staff:
New, Experienced or Non-Experienced in Clinical Research
On-Site Near Your Location (Local/Regional)
On-Going Training (Initial, Refresher)
Classes Focus on:
Knowledge of, Identifying, and Maintaining Compliance
Field-Proven Specific Skills and Techniques
How to become an "A" Ranking site
Expert Monitoring Services (EMS)
Global Clinical Trial Consultants, LLC is a Contract Monitoring Organization that provides monitoring in addition to all aspects of study management. We are dedicated to providing Expert Monitoring Services (EMS) by perfecting the process through study management, GCP training and continuous quality improvement. EMS utilizes a nationwide regionalized structure of clinical research professionals to serve our clients.
Global Clinical Trial Consultants, LLC provides exceptional clinical research services to suit your specific clinical needs by focusing on three principles in the performance of monitoring and study management services: Quality, Standardization and Efficiency.
Standardization
CRA training that involves using a systematic monitoring method and report writing techniques
Study management guidelines
Study material used by CRAs and CRCs
Quality
GCP/ICH expertise and compliance
CRA education and training
SOP compliance
Efficiency
Web-based* GCP/ICH education
Web-based* monitoring management system, which provides the added feature of real time trial milestone tracking of quality indicators
Study planning flexibility and industry competitive pricing structure
Products and Services
Contract Monitors reviews and develops monitoring reports, guidelines and correspondence templates as well as study specific monitoring tools. GCP/ICH educational materials and standardized documents are offered in conjunction with our partnering organization, CRA Solutions, Inc.
Contract Monitors provides the following products and services:
Investigator qualification and site selection
Quality contract monitoring and comprehensive study management
HIPAA compliant Web-based trial management*
Study specific monitoring plan and report development
Regulatory consultation
CRF review and design
Study specific document development and study site binder
Development of SOPs for all aspects of study site management activities
Want to Learn More About EMS?
If you would like more information on EMS and how we can start providing one of the best managed and experienced monitoring services for your company, please contact us at 866-428-3001 or email info@gc-tc.com
Training on the following Topics:
HIPAA/Patient Privacy Laws
Monitoring
Study Coordinator Responsibilities
Clinical Investigator Responsibilities
Clinical Research Consultation
Any Organization, including Sponsors:
Clinical Investigators
Contract Research Organizations (CROs)
Customized Classes
Training for Staff:
New, Experienced or Non-Experienced in Clinical Research
On-Site Near Your Location (Local/Regional)
On-Going Training (Initial, Refresher)
Classes Focus on:
Knowledge of, Identifying, and Maintaining Compliance
Field-Proven Specific Skills and Techniques
How to become an "A" Ranking site
Expert Monitoring Services (EMS)
Global Clinical Trial Consultants, LLC is a Contract Monitoring Organization that provides monitoring in addition to all aspects of study management. We are dedicated to providing Expert Monitoring Services (EMS) by perfecting the process through study management, GCP training and continuous quality improvement. EMS utilizes a nationwide regionalized structure of clinical research professionals to serve our clients.
Global Clinical Trial Consultants, LLC provides exceptional clinical research services to suit your specific clinical needs by focusing on three principles in the performance of monitoring and study management services: Quality, Standardization and Efficiency.
Standardization
CRA training that involves using a systematic monitoring method and report writing techniques
Study management guidelines
Study material used by CRAs and CRCs
Quality
GCP/ICH expertise and compliance
CRA education and training
SOP compliance
Efficiency
Web-based* GCP/ICH education
Web-based* monitoring management system, which provides the added feature of real time trial milestone tracking of quality indicators
Study planning flexibility and industry competitive pricing structure
Products and Services
Contract Monitors reviews and develops monitoring reports, guidelines and correspondence templates as well as study specific monitoring tools. GCP/ICH educational materials and standardized documents are offered in conjunction with our partnering organization, CRA Solutions, Inc.
Contract Monitors provides the following products and services:
Investigator qualification and site selection
Quality contract monitoring and comprehensive study management
HIPAA compliant Web-based trial management*
Study specific monitoring plan and report development
Regulatory consultation
CRF review and design
Study specific document development and study site binder
Development of SOPs for all aspects of study site management activities
Want to Learn More About EMS?
If you would like more information on EMS and how we can start providing one of the best managed and experienced monitoring services for your company, please contact us at 866-428-3001 or email info@gc-tc.com
Global Clinical Trial Consultants, LLC - 207 N. Boundary St. Manning, SC 29102 - info@gc-tc.com - Ph:803.433.1000 - Fax: 803.433.1001