Information for Sponsors

Our research team at RCBM has experience in startup, enrolling and conducting a range of clinical trials. To remain on the cutting edge of technology in clinical research, and maximize the effectiveness of all stages of the research process, we ensure that our procedures are bolstered by innovative and cutting edge technology. Our research team at RCBM has experience in startup, enrolling and conducting a range of clinical trials. We have years of experiencing working and collaborating with numerous sponsors on different protocols for different CNS indications. As technology continues to change, so does our research team and our aptitude to change with new technology. Recently, protocols have started to incorporate more and more technology which comes with a learning curve. Vendors we collaborate with include:

The Clinical Trials Group is committed to administering high quality clinical trials. This means we place a premium on adherence to procedure and safety. We do so by providing measuring and monitoring resources, a highly trained and qualified staff, and rigorous internal processes that allow for timely and correct administration of study procedures.

 Resources

The Clinical Trials Group’s facilities include the following on-site clinical resources among others:

  • CLIA certified Lab
  • Electrocardiogram
  • Secure storage for controlled substances
  • Dedicated monitoring spaces
  • Cutting edge software
  • Statistical analysis software

Staff qualifications

Our staff is trained in GCP and HIPAA. The staff includes licensed health care providers, and all have obtained or are close to obtaining post-graduate degrees and training. Our staff’s training in administering safety and tolerability measures as well as a variety of end point measures ensures quality measurement and monitoring.

Procedures

The Clinical Trials Group prides itself on maintaining appropriate rigor in following regulatory rules and study protocols for every clinical trial. Our standard operating procedures include:

  • HIPAA safeguards for personal identifying information
  • Patient screening
  • Regular monitoring of safety and tolerability
  • Initiation and close out procedures
  • On-site availability of PI and medical staff
  • Accurate and efficient maintenance of study records and files
  • Regulatory binder maintenance
  • Drug accountability 
  • Drug dispensing
  • Regular upgrades to technology 
  • Clean and safe patient rooms