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ERA offers CRO services that save time and contain costs

ERA Clinical is proud to offer a range of traditional CRO services—all based on our years of experience, innovative methodologies, and unique processes—developed to save time and contain costs. Our broad range of services support:
  • Clinical trials
  • Medical device trials
  • Registries (observational)
  • OTC switch studies
  • Consulting services

Clinical Trials

ERA has developed tools and tactical plans for simple Phase IIIb and Phase IV clinical trials that will get your study up and running in record time. Our processes and tools provide maximum support for your Investigators, ensuring data quality with little time spent resolving data queries. Rely on ERA to:

  • Build study kits for your Investigators with the tools and supplies necessary to perform all study functions
  • Partner with Nurse Practitioners Organizations whose members are available as Principal Investigators, keeping costs low and quality high
  • Provide EDC tools and GCP training to ensure consistency and compliance
  • Utilize a “Risk-Based Central Monitoring” process that helps eliminate unproductive and costly monitoring visits
  • Maintain a progressive virtual structure that keeps overhead low and provides expertise as needed
Medical Device Trials
  • Design and management of your device trials, whether 510K registrations, clinical use, or OTC switch
  • Therapeutic and diagnostic expertise
  • Regulatory expertise
Registries
  • Design of registry and observational studies that will meet your regulatory goals and targets
  • Utilization of simple, yet robust, electronic data capture (EDC) systems that provide an accurate and inexpensive platform for long-term data collection and management
  • A tailored and efficient combination of risk-based and traditional monitoring, specific to the needs of each registry
OTC Switch
  • Management of focus groups to help design your label and advertising
  • Design and execution of Label Comprehension studies to support your application
  • Evaluation of Actual Use effectiveness data for your submission
Other Consulting Services
  • Regulatory
  • Medical Writing
  • Biostatistics
  • Monitoring

To discuss your specific needs with an expert at ERA Clinical, call 877-777-ERA1 or use the convenient form in Contact Us.


 
 
 
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IIT, IIS, IIR, IIS, ISR, IST, KOL, MSL, medical affairs, Phase IV, investigator initiated trials, post marketing, post marketing, key opinion leader, medical device; ERA Clinical is the CRO for Investigator Initiated Trials, medical Device and Streamlined Clinical Trials. Quality, Cost & Speed, along with innovative systems & technology offer unparalleled value.