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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
