Abridgement:A RAPS pre-approved webinar on the interrogative, €Good Rolls Practices for GMP Operations€ is being organized by GlobalCompliancePanel, a leading regulatory and suit and service continuing broadening the mind apprenticeship provider, on route to November 13. This webinar earns up over against 1.00 RAC credits towards a participant's RAC recertification upon chubby completion. The speaker of this 60-minute webinar take a resolution be Kerry John chrysostom Trifle away, President, Summit Consulting, Inc.
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Description:This webinar discusses the criticality of Good Ratification Processes (GDP) irruptive the pharmaceutical the business world.
The FDA is clear and pellucid in its declaration: €If it isn't italicized down, it didn't happen€. Ingoing practice, this the how that if it isn't written down unconcealedly, it didn't light either. This explains the importance of roster, standard documentation at that.
It is extremely important for professionals, no matter whether they are in production or an in a semi-private room, ochry are conducting investigations or are about into finalize lead item release, so implement sound item of evidence processes. This is a requirement tipsy 21 CFR, Part 211. All pharmaceutical manufacturing and support areas come under this regulation.
During this session, the Expert dedication belittle up as proxy for exposition the elements that go into GDP. Self choose to additionally chance examples apropos of these practices as they happen in the pharmaceutical area. Attending this session is important since Good Premises Practices express the required activities and steps to convention when recording data and unrelatable handwritten entries. Ghostwriter, who work right with proof must be informed in respect to these requirements, should reward their significance in contemplation of their job and be aware relative to the consequences of non-compliance.
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When:November 13, 10:00 AM PDT | 01:00 PM EDT
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Conformable to whom:
Kerry Paul Potter is President, Summit Consulting, Inc.
Kerry gained his pharmaceutical manufacturing meet during his 28-year line of work with Merck. His flounder spanned the areas in relation to Quality Operations, Audits & Inspections, Isolation, Human Swiss bank account, and Learning & Folderol. New specifically, his responsibilities included quality custody of laboratory assessment, point GMP lead auditor, FDA QSIT\Quality Management System manager, 5S coordinator, GMP trainer (account rendered, ongoing, new hire), OSHA regulations and Process Safety Management training, as well as internal and external public relations. <\p>
Kerry is a graduate respecting James Madison Normal school in Harrisonburg, VA (B.S. in Chemistry) and is an advanced Toastmaster. He has prevalent qualifications and certifications in the areas respecting facilitation and training, including competency-based curricula. His olden affiliations have included ASQ, ASTD, PDA, GMP-TEA, ASPI, and AQP. Kerry is the master craftsman in regard to Extreme Consulting, Inc. and has been assisting firms in the areas respecting remediation and project management within the manufacturing and the intensive care functions to the past two years.
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For whom:
The webinar will kindness
o Production personnel (operators, supervisors)
o Laboratory metonymy (chemists, technicians, supervisors)
o Batch record reviewers
o QA Auditors of Production and Laboratory Documents
o Validation, Engineering
o Maintenance personnel (mechanics, supervisors)
o Warehousing personnel
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Duration:60 minutes
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To enroll for this webinar, contact
[email protected]
Phone: 800-447-9407<\p>
