Why Should You Attend:
Familiarity with the clinical protocol permits resource allocation (reagents, instruments analytical, QA and QC personnel) to ensure efficient and timely analysis and reporting. In addition to the resources, attention to the specific informed consent and sample directives reduce the risk of facing regulatory and legal issues. This is to ensure not only that reported results are in the correct format, but also to understand what the subject has agreed to in terms of sample handling, disposition, storage and use.
Application of a patient’s sample to something not agreed upon in the protocol or specifically proscribed in the protocol can lead to personal charges against the clinical trial sponsor and FDA findings of non-compliance. This presentation will discuss responsibilities of the lab in supporting subject requests and orders.
This review will cover the development, evolution and application of Good Clinical Practice, (GCP) and will discuss responsibilities of lab personnel in maintaining GCP, observing and enforcing specific blinding protocols, maintaining the integrity and privacy of personal health information under HIPAA and GDPR.
Because bioanalytical personnel are not generally the drivers, the approach suggested is to identify possible issues and to discuss with the clinic approaches to minimize risk- for example assigning accession numbers to samples and associated documents such that the lab does not “see” or record any personal identification which can be traced and identify trial participants. Specific attention will also be directed at understanding patient directives regarding results and samples.
Areas Covered in the Webinar:
Who Will Benefit:
Dr. O’Connor has been a Director, Manager and Consultant in regulated Analytical and Bioanalytical laboratories in Pharma, Biotech and CROs for over 25 years. He has had direct involvement in lab relocation and design, method development, method, process and instrument/equipment validation.
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.If you have any concern about the content of the webinar and not satisfied 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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