Biogenics Research Chamber can conduct Phase I-IV studies and has the experience and expertise needed to achieve the objectives for each study.  All clinical research is conducted to the standards of Good Clinical Practices.  Our services and experience include:

  • Support in Protocol Design and Planning
  • Project/Data Management
  • IRB Submission
  • Internal and Regulatory Quality Assurance
  • A research team with 35+ years of clinical research experience
  • Ophthalmologists experienced in clinical research
  • Full Data Documentation