3-hr Virtual Seminar: Annual ICH GCP Refresher Course

Speaker

Instructor: Christine Hegi
Product ID: 702652
Training Level: Intermediate to Advanced

Location
  • Duration: 3 hrs
This 3-hr virtual seminar will offer a comprehensive ICH GCP training for all healthcare professionals involved in clinical research.
RECORDED TRAINING

 

$399.00
1 USB is for usage in one location only. info CD/USB and Ref. material will be shipped within 15 business days
(For multiple locations contact Customer Care)

 

 

Customer Care

Fax: +1-650-362-2367

Email: [email protected]

Read Frequently Asked Questions

Why Should You Attend:

It is required that all healthcare professionals involved in clinical research must have documentation of current ICH GCP training. It is also required that that staff involved in clinical research update their ICH GCP training on a yearly basis. This training will help you fulfill this requirement.

This 3-hr virtual seminar is designed to provide a comprehensive training on ICH GCP guidelines. It is designed to offer documentation of comprehensive ICH GCP training required by regulatory agencies and sponsors. Participants will learn why ICH GCP has been adopted worldwide as the standard for ethical research practices and how to implement ICH GCP in their daily processes.

Areas Covered in the Webinar:

The webinar will include the following critical information you will need:

  1. Background information on the need for standardized GCP guidelines for the clinical research industry.
  2. Coverage of ICH requirements for the Investigator.
  3. Coverage of ICH requirements for the Sponsor.
  4. Coverage of ICH requirements for IRBs.
  5. Subject rights.
  6. Adverse Event and Serious Adverse Event reporting.
  7. Essential document requirements.
  8. Document retention requirements.
  9. Best practices and fraud.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel/ companies in the clinical research industry. The employees who will benefit most include:

  • Principal Investigators
  • Research Nurses
  • Study Coordinators
  • Site Regulatory Personnel
  • Clinical Research Site Administrators
  • Sponsor site selection personnel
  • CRAs
  • Quality Assurance
  • Documentation professionals both at the site and sponsor companies
  • Healthcare professionals needing to acquire documentation of current ICH GCP training.

Instructor Profile:

Christine Hegi, RN, CCRP is the Founder and President of Hegi Research Corp. headquartered in Calgary, AB, Canada, which is a group of Independent CRAs offering clinical research consulting, auditing, site management and monitoring services to the pharmaceutical industry. Ms. Hegi has clinical research experience as the Global Project Manager for several large, multinational studies and has over 20 years of extensive experience in all phases of drug and device development.

Christine is the author of SOPs for Clinical Research Sites© which is a comprehensive set of Standard Operating Procedures available for purchase. These SOPs are unique in that they are designed to be customized by the site and to be utilized as a training tool for site staff.

Ms Hegi has authored and instructed CRA training courses for some of the major pharmaceutical companies as well as small organizations. She has taught multiple courses in SOP development and utilization. Multiple academic organizations have contracted her services for the presentation of ICH GCP and other research related courses. She has presented multiple times at professional conferences. Her previous experience as an Emergency Nurse, Study Coordinator, CRA and Director of Clinical Affairs bring both site and industry perspectives to her teaching.

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Refund Policy

Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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