Affordable Remote Site Service (RS2) Options
Covigilant Research is committed to working together with you and providing exceptional value in every service we offer.
Covigilant Research understands that most clinical sites are extremely busy with the day-to-day responsibilities of providing patients with high-quality health care. The necessary paperwork and record-keeping associated with clinical trials can seem to inundate.
We have over 30 years of experience in managing clinical trial research and want to share our affordable solutions for managing clinical trial data.
Our Options Provide You With Exceptional Value
Covigilant Research, LLC offers subscribers a regular free list of clinical trials; free onsite recruitment advertising; an affordable validated, 21 CFR part 11 eReg & eSource application; and, the option for sites to pick and choose the services we offer that suit their needs.
Our RS2 Application Provides Research Sites:
- A private, validated, 21 CFR part 11, HIPAA compliant platform
- Fully customizable database for each study
- Controlled file access
- Complete audit trail
- Track all file activity
- Be ready at all times of site audits
- A platform for remote site audits
- Learn how to add and remove the prebuilt categories within the study directory
Your Study Folder
Your Study Folder Is Ready!!
Your RS2 eRegulatory and eSource preset folders are ready for your customization and use.
After subscribing to the RS2 system, we will email your RS2 access URL to you. Additionally, your login credentials and instructions will follow.
If additional assistance is required or you have any questions please contact Covigilant Research RS2 Technical Support (rs2@covigilantresearch.com or (877) 994-2272 ext 3)
When you choose the CRC Assist package, which includes the RS2 application for the duration of your trial, you will receive a custom eBinder, eSource, and complete site assistance during the regulatory approval phase of your clinical trial.
Don’t forget both RS2 and CRC Assist Subscribers have access to our free study advertising.
Never Guess About A File Again!
Our System Tracks All File Activity
With our trial data solution package, you will no longer have to worry about the status of a file.
Additional Site Services | We Will Work With You
Do You Need More or Specialized Services?
We understand.
Without Longterm Contracts…
Choose what Additional Services you need.
Customized Service Options
Additional Services May Include
Administrative
- IRB Submission & Approvals
- E-Regulatory
- Contracting & Budgets
- Study Payments, Invoicing, & Stipends
- Recruitment Campaigns
- Professional Training & CV Updates
- Call Center
Pre-Trial
- Trial Identification & Matching
- Investigator Database Submission & Updates
- Sponsor Outreach & Advocate
- Creation & Maintenance of Source Documentation
- Study Start-up
- Site Study Feasibility
- Site Selection Visit (SSV) & Site Initiation Visit (SIV) Preparation
Trial Period
- Online Charting
- E-Consent
- Televisits
- Electronic Data Capture (EDC) / Query Resolution
- Participant / Patient Scheduling
- Participant Pre-Screening
- Enrollment / Participant Tracking
Affordable Trial Data Management Solutions
RS2 Remote Access
eReg & eSource- Base e-Regulatory & eSource
- Online Charting
- Site Monitoring Assistance
RS2 + CRC Assist
Single Site / Single Study & RS2- Start-up E-Binder
- Regulatory Approval Prepartion
- Supervise *IRB Submissions & Approvals
Additional Services
Choose What Services You Need- Televisits
- EDC Completion
- Participant Recruitment
We offer three value packed options to manage your trial data.
- If you are interested in the basic plan please click or tap on the click here button at the bottom of the CRC Assist column.
- If you would like us to manage your files for you, along with managing your study remotely please select the click here button at the bottom of the CRC Remote column.
- If you need assistance managing any portion of your trial, please call us immediately for assistance. Pricing will be based on the service(s) you need.
