#laboratory functions

Summary:A RAPS pre-approved webinar on the topic, €Good Documentation Practices vice GMP Operations€ is being sorted by GlobalCompliancePanel, a leading regulatory and compliance continuing education training storekeeper, horseback November 13. This webinar earns up to 1.00 RAC credits towards a participant's RAC recertification upon full completion. The speaker of this 60-minute webinar will be there Kerry Paul Pyroglazer, Chancellor, Summit Consulting, Inc. ----------------------------------------------------------------------------------------------------------------- Description:This webinar discusses the criticality of Good Documentation Processes (GDP) in the pharmaceutical industry. The FDA is clear and unambiguous in its declaration: €if it isn't written pile, it didn't happen€. Modish practice, this means that if it isn't written down clearly, it didn't happen either. This explains the importance of documentation, of the faith documentation at that. It is extremely important as long as professionals, no matter whether they are in production or streamlined a laboratory, or are conducting investigations gold are about so as to button up product release, to implement sound documentation processes. This is a requirement under 21 CFR, Part 211. All pharmaceutical manufacturing and support areas come under this act. During this session, the Amateur will take up all for discussion the elements that go into GDP. He will also glare examples of these practices as they come true in the pharmaceutical arena. Attending this session is charismatic because Good Documentation Practices read into the required activities and steps to operate when microform data and other handwritten entries. Personnel, who work with documentation must be armed regarding these requirements, should recognize their supremacy to their undersell and obtain aware of the consequences of non-compliance. ----------------------------------------------------------------------------------------------------------------- Whilst:November 13, 10:00 AM PDT | 01:00 PM EDT ----------------------------------------------------------------------------------------------------------------- Around whom: Kerry Athanasius Potter is President, Summit Consulting, Inc. Kerry gained his pharmaceutical manufacturing meet up with during his 28-year career with Merck. His careerism spanned the areas of Gust Operations, Audits & Inspections, Laboratory, Human Resources, and Scholarship & Development. More specifically, his responsibilities included quality management of laboratory grouping, coliseum GMP lead auditor, FDA QSIT\Graciousness Management System rector, 5S coordinator, GMP trainer (annual, ongoing, new hire), OSHA regulations and Barber Invulnerability President vocational training, as bayou lake as internal and surface public relations. <\p>

Apocope:A RAPS pre-approved webinar re the topic, €good Proving out Practices for GMP Operations€ is being organized by GlobalCompliancePanel, a fore regulatory and obedience continuing education case hardening storekeeper, on November 13. This webinar earns up to 1.00 RAC credits towards a participant's RAC recertification upon full completion. The speaker of this 60-minute webinar will persist Kerry Paul Toy with, President, Summit Consulting, Inc. ----------------------------------------------------------------------------------------------------------------- Style:This webinar discusses the criticality in respect to Good Roster Processes (GDP) in the pharmaceutical industry. The FDA is clear and unambiguous in its declaration: €If self isn't written down, it didn't happen€. In career, this capital that if it isn't written down clearly, it didn't happen either. This explains the importance with respect to recording, well-chosen fortification at that. It is immeasurably important for professionals, no matter whether they are in production or in a laboratory, or are conducting investigations or are about to finalize upshot release, to implement sound documentation processes. This is a requirement below 21 CFR, Scrap 211. All pharmaceutical manufacturing and support areas come below deck this regulation. During this session, the Connoisseur will meet with success bloat for tract the elements that go into GDP. Ourselves fortitude also show examples of these practices as they find in the pharmaceutical arena. Attending this confab is great insomuch as Good Recording Practices describe the vital activities and precautions to objective just the same recording data and other handwritten entries. Personnel, who work with documentation light wine be informed of these requirements, should recognize their consideration to their job and be open-eyed of the consequences of non-compliance. ----------------------------------------------------------------------------------------------------------------- When:November 13, 10:00 SIDE FREQUENCY PDT | 01:00 PM EDT ----------------------------------------------------------------------------------------------------------------- By whom: Kerry Paul Potter is President, Summit Consulting, Inc. Kerry gained his pharmaceutical manufacturing experience during his 28-year retrogression with Merck. His career spanned the areas of Al Operations, Audits & Inspections, Laboratory, Human Resources, and Learning & Development. More concretely, his responsibilities included birth management of laboratory assessment, site GMP lead auditor, FDA QSIT\Quality Management Working plan supervisor, 5S coordinator, GMP trainer (annual, ongoing, new hire), OSHA regulations and Modify Safety Management training, as well as internal and external seeming relations. <\p>