Regulatory

  • Program Strategy, Roadmap, Guidance
  • FDA Meetings
  • Modules 1, 2, 3 Authoring, Formatting, and Submission
  • Controlled Correspondences and Electronic Communications to Health Authorities such as:
  • Deficiency Letter Responses
  • Suitability Petitions
  • Comparability Protocols
  • Audits and Inspection Readiness