New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally

This webinar will help clinical laboratories, analyzing samples from clinical trials, understand the

compliance requirements concerning ICH GCP for FDA and EMA (new requirements 2012)

compliance.

Why Should You Attend:

As a result of the FDA and EU Clinical Trials Directive 200/20/EC and subsequent promulgation of laws, EMA inspection and reflection paper in clinical laboratories in the EU covering the

conduct of clinical trials in accordance with Good Clinical Practice (GCP), there is the need for laboratories undertaking analysis of samples from clinical trials to comply with GCP regulations and guidance. The standard to be followed by such laboratories is not well defined in FDA and ICH GCP and hence the development of new EMA standards (finalized in 2012) which provides guidance on the standards which will set the gold standard in the EU, US and potentially

internationally.

This session will review the key requirement for compliance for the analysis of samples collected from subjects participating in clinical trials and forms a key part of the clinical trials process. It is essential that sample analysis and evaluation is performed to an acceptable standard which will ensure patient safety is not compromised and that data is reliable and accurately reported.

This presentation will explain the new standards required by laboratories analyzing clinical trial

samples. The session is aimed at both sponsors using clinical laboratories and those at laboratories who wish to demonstrate to sponsors of clinical trials and government agencies

worldwide that the clinical laboratory operates to a standard that assures the reliability, quality and integrity of the work and results generated.

Areas Covered in this Webinar:

What does GCP and the new guidance require of clinical laboratories? What parts of GCP apply to clinical laboratories?

What standards should the laboratory be working to? How to assess a clinical laboratory? Sponsor companies should assess the laboratory

before placement to ensure that all aspects of GCP are satisfactorily addressed and that the laboratory standards and methods meet GCP requirements.

Facilities, to assess the orderliness, cleanliness and environmental suitability of premises where study specific activities are to be carried out and the arrangements for storage of materials and samples.

Procedures for sample collection, receipt and application of acceptance/rejection

criteria and for the preparation of reagents. What documentation should be available – including SOPs, validation, technical

agreements? What is required to ensure quality and appropriateness of methodology in use in any

laboratory? What should be included in the contract between the laboratory and the sponsor? What is the role of the sponsor company and laboratory during the study for ensuring

clinical trials sample management and analysis meet GCP requirements?

Who will benefit:

This webinar will provide critical assistance to FDA and EMA regulated companies currently carrying out or preparing to conduct clinical trials for pharmaceutical, biotechnology, and biologics products using clinical laboratories. It will also be applicable to personnel working in clinical laboratories.

Clinical Development managers and personnel Clinical research associates

Clinical Research archiving and document management personnel Quality assurance managers and auditors

Clinical Development managers and personnel CROs using laboratories to analyze clinical trial samples Sponsors and non-commercial sponsors Sponsors who have their own laboratories for analyzing clinical trial samples Consultants Laboratories analyzing samples from clinical trials

For more details visit us at: https://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703094?channel=Doc_organic