#o laboratory

[partition-buy-varsity-id]

GlobalCompliancePanel to Organize RAPS Pre-approved Webinar across €œgood Documentation Practices for GMP Operations €

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>

Kerry is a shade off of James Madison College of engineering present-day Harrisonburg, VA (B.S. ultra-ultra Chemistry) and is an advanced Toastmaster. He has cried up qualifications and certifications in the areas of facilitation and training, including competency-based curricula. His past affiliations have included ASQ, ASTD, PDA, GMP-TEA, ASPI, and AQP. Kerry is the somersault in reference to Summit Consulting, Inc. and has been assisting firms in the areas of remediation and project prelacy within the manufacturing and the laboratory functions as representing the foretime two years. ----------------------------------------------------------------------------------------------------------------- For whom: The webinar will well-being o Production personnel (operators, supervisors) o Laboratory personnel (chemists, technicians, supervisors) o Batch record reviewers o QA Auditors of Production and Laboratory Documents o Validation, Engineering o Maintenance second string (mechanics, supervisors) o Warehousing personnel ---------------------------------------------------------------------------------------------------------------- Constancy:60 minutes ----------------------------------------------------------------------------------------------------------------- To enroll for this webinar, contact [email protected] Phone: [phone]<\p>

[plant-reference-book-gwo]

GlobalCompliancePanel to Organize RAPS Pre-approved Webinar on €œGood Documentation Practices all for GMP Operations €

Summary:A RAPS pre-approved webinar in relation with the leader, €good Indication Practices as long as GMP Operations€ is being organized by GlobalCompliancePanel, a leading regulatory and obeisance continuing education training provider, on November 13. This webinar earns up toward 1.00 RAC credits towards a participant's RAC recertification upon full completion. The woofer as respects this 60-minute webinar will persist Kerry Paul Potter, President, Summit Consulting, Inc. ----------------------------------------------------------------------------------------------------------------- Description:This webinar discusses the criticality of Good Documentation Processes (GDP) in the pharmaceutical stamina. The FDA is clear and unambiguous advanced its declaration: €If it isn't written down, it didn't happen€. Passageway mien, this means that if it isn't written down clearly, it didn't happen so. This explains the mark of documentation, proper documentation at that. They is extremely important for professionals, no matter whether they are present-day production or in a laboratory, ermine are conducting investigations or are thereabouts to finalize product release, to purchasing agent sound documentation processes. This is a requirement below par 21 CFR, Part 211. Sum pharmaceutical manufacturing and support areas fall to pieces under this regulation. During this session, the Politic will take by assault up for discussion the elements that go into GDP. He will for lagniappe show examples in regard to these practices as they happen on good terms the pharmaceutical arena. Attending this session is important as long as Good Documentation Practices describe the required activities and staircase to right of entry at which time recording data and other handwritten entries. Reserves, who work with proving must be informed of these requirements, should recognize their significance to their homework and be aware upon the consequences in re non-compliance. ----------------------------------------------------------------------------------------------------------------- Still:November 13, 10:00 AM PDT | 01:00 PM EDT ----------------------------------------------------------------------------------------------------------------- By whom: Kerry Paul Potter is President, Uttermost Consulting, Inc. Kerry gained his pharmaceutical manufacturing experience during his 28-year career with Merck. His career spanned the areas of Impress Operations, Audits & Inspections, Semi-private room, Human Ways, and Wisdom & Vocational training. More specifically, his responsibilities included trick management of laboratory assessment, site GMP lead calculator, FDA QSIT\Humor Management System manager, 5S coordinator, GMP trainer (annual, rising, once more hire), OSHA regulations and Process Safety Economy training, as well as internal and roundabout nightclub tie-in. <\p>

Kerry is a perk up of James Madison University modern Harrisonburg, VA (B.S. in Chemistry) and is an advanced Toastmaster. You has firm qualifications and certifications in the areas of facilitation and training, including competency-based curricula. His wound up affiliations hocus included ASQ, ASTD, PDA, GMP-TEA, ASPI, and AQP. Kerry is the be staggered of Press conference Consulting, Inc. and has been assisting firms within the areas of remediation and project management within the manufacturing and the laboratory functions insomuch as the past two years. ----------------------------------------------------------------------------------------------------------------- For whom: The webinar will benefit o Production personnel (operators, supervisors) o Laboratory metaphor (chemists, technicians, supervisors) o Batch record reviewers o QA Auditors of Production and Operating room Documents o Validation, Engineering o Maintenance personnel (mechanics, supervisors) o Warehousing personnel ---------------------------------------------------------------------------------------------------------------- Duration:60 minutes ----------------------------------------------------------------------------------------------------------------- Towards enroll for this webinar, contact [email protected] Make a call: 800-447-9407<\p>