How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters

Instructor: Leonidas Lambrinidis
Product ID: 701793
  • Duration: 60 Min
This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense.

recorded version

1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Oct-2011

Training CD / USB Drive

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

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Read Frequently Asked Questions

Why Should You Attend:
Applying GCP in a real life situation is often subjective, requires experience and training. A Clinical Trial, like any other project is divided in stages with tasks running in parallel or in sequence and affecting one another in a cause and effect relationship. Over the years, findings of inspectors and experiences of monitors have identified clusters of deficiencies in complying with GCP principles, key areas that emanate straight from the GCP guidelines.

This presentation will shed light on what one needs to pay attention to, in order to run a clinical trial in a GCP compliant manner, securing both results and quality. By defining the key parameters and providing lists of common deficiencies, an understanding of how to progress through each stage of a project and what to watch out for will be gained. As a result, working knowledge of GCP will increase.

Areas Covered in the Seminar:

  • Importance of Good Clinical Practice.
  • Key areas of deficiencies in Clinical trials.
  • Common findings in audits and inspections.
  • Definition of ranking of findings: minor-major-critical.
  • Definition of Adverse and Serious adverse events.
  • ICH guidelines on the Informed consent process.
  • Management of investigational drug.
  • Investigator site file and essential documents.
  • Source data.
  • Site and people management.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in: Pharmaceutical, Biotechnology, CROs and Research Facilities Conducting Clinical Trials including:
  • Managers in Clinical Development and Project Leaders
  • Quality Assurance Managers and auditors
  • Clinical Research Associates
  • Clinical Operations Staff
  • Regulatory Compliance Associates and Managers
  • Investigators, site coordinators and subinvestigators

Instructor Profile:
Leonidas Lambrinidis, BSc Biochemistry, MSc Biochemical Engineering, MBA. 10 years in clinical research. Held various positions in the industry from CRA to Associate director of project management. Worked both in the Pharmaceutical industry and CROs. Experience in sponsor, FDA and EMA inspections. Conducted both internal and external trainings.

Follow us :
Seminars by Ex-FDA Officials
Latin America: Regulatory Compliance Requirements for Life Science Products

Refund Policy

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.

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