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Working With Us

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Keeping it Simple

Clinical drug development is complicated. I2R works with each of our clients…

Clinical drug development is complicated. I2R works with each of our clients to keep protocols and data collection as simple and straightforward as possible. We know that the lack of simplicity leads to errors in implementation and poor data quality which ultimately cost more time and money.

Adding Value

Too many CROs view staff as a commodity where CRAs, Project Managers…

Too many CROs view staff as a commodity where CRAs, Project Managers and Data Managers are interchangeable. I2R takes a different approach. Each team member is invested in your project and adds value with demonstrated expertise. We will ask questions and propose solutions and complement your team with our years of experience and knowledge of best practices. We will offer creative alternatives that meet the needs of the trial because we have the track record to know what works and what doesn’t.

Investing in Relationships

Clinical trials often last a long time…

Clinical trials often last a long time so the relationships between parties are a critical component of a program’s success. We recognize that building an open, honest, productive relationship, and cultivating real camaraderie with your team goes a long way towards running a successful program. Strong relationships with our clients lead to good outcomes on the projects.

Communicating

Clinical drug development requires teams from many disciplines…

Clinical drug development requires teams from many disciplines. Physicians, statisticians, data managers, operations personnel, clinical research associates and medical writers must all work together for a program to be successful. Too many companies work in silos, and as a result obstruct the flow of critical information across functions. In contrast, I2R efficiently and effectively involves all team members in providing input for key deliverables. This allows each area to apply their expertise early in the planning phases and lessens the probability of significant revisions once the trial is live.

Thinking Smart

The unexpected will occur during the conduct of a clinical trial…

The unexpected will occur during the conduct of a clinical trial. We rely on our breadth of experience to anticipate problems and plan for contingencies. I2R is invested in conducting the best run clinical trials to meet your objectives and get the best possible performance from the sites.

What We Do

IND/CTA Preparation and Submission

  • Document Production
  • Document Publishing
  • Electronic Publishing
  • IND Maintenance

Clinical Trial Management

  • Project Management
  • Site Selection and Startup
  • Site Monitoring
  • Medical Monitoring
  • Database Build
  • Data Management
  • Biostatistics
  • Pharmacokinetics
  • Clinical Study Report

Regulatory and
Medical Writing

  • IND/CTA Modules
  • Investigator Brochures
  • Investigational Medical Product Dossiers
  • Protocols
  • Consent Forms
  • Study Manuscripts

Other Services

  • Clinical Development Planning
  • Clinical Program Budgeting
  • Regulatory Strategy and Representation at the FDA
  • Establishment of Clinical/Scientific Advisory Boards
  • Data Safety Monitoring Board Administration and Support
  • GCP Auditing

Who We Are


Contact Us

If you are interested in working with our team,
please contact us.

Corporate Offices
IND 2 Results, LLC
1904 Monroe Drive, NE, Suite 140
Atlanta, GA 30324