Inspection Readiness Training

This 1-day accredited course equips Sponsor, CRO, site, and compliance personnel with the knowledge, practical tools, and strategies to achieve and maintain regulatory inspection readiness, including preparation, CAPA, and best practices for successful outcomes.

Inspection Readiness for Clinical Trials

This course targets Sponsor personnel, CRO personnel, Investigators, Site staff, and Compliance teams involved in inspection readiness activities.

Participants will:

  • Understand the difference between inspection preparedness and readiness.
  • Identify triggers for regulatory inspections.
  • Learn critical steps to achieve and maintain inspection readiness.
  • Recognize inspection types, preparation strategies, and processes.
  • Explore best practices for responding to observations, including corrective and preventive actions (CAPA).
  • Gain practical knowledge through lectures, case scenarios, checklists, and interactive Q&A.
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Participants will:

  • Understand the difference between inspection preparedness and readiness.
  • Identify triggers for regulatory inspections.
  • Learn critical steps to achieve and maintain inspection readiness.
  • Recognize inspection types, preparation strategies, and processes.
  • Explore best practices for responding to observations, including corrective and preventive actions (CAPA).
  • Gain practical knowledge through lectures, case scenarios, checklists, and interactive Q&A.
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Course Format

Participants will gain knowledge through lecture, case scenarios, checklists and interactive Questions and Answers.

 

Attendees will receive a certificate for successfully attending and passing the Inspection Readiness Assessment.

CPD Accreditation

Certification is issued upon successful completion of the course and assessment.

Cost

R3000.00

VAT is not applicable.

Booking/Registration

Complete our registration form online, or use the contact details below, and we’ll provide you with more information.

Register Online

HPCSA-Accredited Training Provider

With a professional learning environment and all the resources you need, we are confident this course will be a valuable fit for your professional development—whether you are here to build foundational knowledge or to renew your GCP certification.

“For any questions or support, please reach out—we’re here to assist and look forward to your participation.”

Frequently Asked Questions

1. Who should attend this course?


Sponsor, CRO, site staff, investigators, and compliance personnel involved in inspections.

2. What does the course cover?

Inspection readiness, types of inspections, preparation, checklists, and corrective actions (CAPA).

3. How is the course delivered?

1-day classroom-style with interactive lectures, case scenarios, and Q&A.

4. What is required for certification?

Yes, attendees receive a certificate after completing the training.

5. What is the cost?

R3,000 per person (VAT not applicable).

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Quick Course Summary

  • For Who:
    Aimed at sponsor, CRO, site staff, investigators, and compliance personnel.
  • Content Covered:
    Covers inspection preparedness vs readiness, triggers, processes, and outcomes.
  • Skills:
    Provides practical tools, checklists, and case scenarios for inspection preparation..
  • Format:
    Delivered 1-day classroom-style with interactive lectures and Q&A.
  • Certification:
    Certificate awarded upon successful completion. Cost: R3,000 (VAT not applicable).

Ready to get started?

Should you require any information, if you want to book your place on a course, or would like to discuss training options, please contact us.

Contact Details

Phone: +27 83 225 9656
Email: info@rrtraining.co.za

Course Registration

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Start and improve your clinical research journey with flexible and accessible GCP and clinical research courses, facilitated by a Clinical Research Expert Consultant with extensive and long-standing experience in the clinical trial industry.

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