Contract Monitors provides exceptional research services to suit your specific clinical needs by focusing on three principles in the performance of monitoring and study management services: Standardization, Quality and Efficiency.

Standardization

• Experienced monitoring team with an emphasis on former graduates of Medical Research Management, Inc.
• 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

• 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

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 QMS?

If you would like more information on QMS and how we can start providing one of the best managed and experienced monitoring services for your company, please contact us at 617-393-9708 or email at QMS@contractmonitors.com

*offered in conjunction with our partnering organization, CRA Solutions, Inc.