Date: | August 1, 2019 - 8:30am - August 2, 2019 - 4:30pm |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | Venue to be announced shortly, Boston, MA, 02101, United States |
Website for Event: | https://www.complianceonline.com/human-error-reduction-program-gmp-environments-... |
Topic: | Seminars and Workshops |
Description: | If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconvenience, you must do it because the regulation requires it. This training will provide you with the steps required to help you implement a Human Error Reduction Program at your site. It includes practical tools, and how to measure effectiveness to continuously improve human reliability at your site. The CFR - Code of Federal Regulations Title 21 Subpart B_Organization and Personnel Sec. 211.22 talks about the “Responsibilities of quality control unit.” and it states that “(a) There shall be a quality control unit that shall have the responsibility and authority to approve or reject all components, drug product containers, closures, in-process materials, packaging material, labeling, and drug products, and the authority to review production records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated…” Also, the European Commission reads “Where human error is suspected or identified as the cause; this should be justified having taken care to ensure that process, procedural or system-based errors or problems have not been overlooked if present. Appropriate corrective actions and/or preventative actions (CAPAs) should be identified and taken in response to investigations. The effectiveness of such actions should be monitored and assessed, in line with Quality Risk Management principles.” |
Contact Name: | Ashutos Swain |
Contact Email: | referral@complianceonline.com |
Contact Phone: | 8887172436 |