• Pharmaceutical / Biotechnology / Biologics
• Medical Device
  • Manufacturing
  • Clinical Trials
  • Sales and Marketing
  • Supply Chain / Subcontractor Management
  • Ethics and Corporate Responsibility
  • Case Studies
• Health Care
• Energy
• Engineering & Construction
• Manufacturing & Services
• Government & Non-Profits

Kaplan EduNeering's clinical trial solutions accelerate product approval by minimizing delays and regulatory noncompliance in the conduct of clinical trials. We work with companies to assure the knowledge and compliant performance of employees, study site personnel, and CROs at dispersed locations around the world.

Proven Learning Management Platform

ComplianceWire, our learning management platform, distributes, tracks and electronically documents good clinical practice (GCP) knowledge, protocol understanding, electronic data capture (EDC) proficiency, and SOP training for investigators, contractors, and employees.

FDA-Authored and/or Reviewed Courses

Kaplan EduNeering’s clinical curricula, developed with the FDA and Association of Clinical Research Professionals (ACRP), are used by investigator sites around the world, including the National Institutes of Health.

Solutions that Solve Key Clinical Compliance Challenges

Kaplan EduNeering assists companies achieve global study compliance with study protocols and regulatory requirements of the FDA, ICH and EU, including:

• GCP/ICH proficiency
• EDC training
• Protocol understanding among sponsor, site, and CRO personnel
• Financial Disclosure Attestations
• Preparation for ACRP Certification of CRA, CRC, and Investigator
• Distribution and documentation of clinical study communications (safety updates, protocol amendments, etc.)
• Cost