Understanding GxP (GMP, GCP & GLP) for FDA Regulated Industries

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Microrite, Inc. brings you this unique learning experience in Understanding GxP (GMP, GCP & GLP) for FDA Regulated Industries; Part of Microrite s step-by-step webinar series. Understanding GxP (GMP, GCP & GLP) for FDA Regulated Industries FDA GxP standards are constantly shifting. Your company s GxP compliance systems must be able to meet this challenge proactively to prevent any disciplinary actions that may be imposed by the FDA due to non-compliance, which can result in delayed premarket approval or product recalls in the worst case scenario. GxP compliance must be able to account for an appropriate level of risk management as well as establish policies and procedures. When? October 16 th, 2014 1:30pm to 3:30pm Eastern Standard Time Which industries does this webinar apply to? Pharmaceuticals, Biotechnology, Cosmetics, Medical Devices, and In Vitro Diagnostics Who will benefit? Quality Assurance, Quality Control, Microbiology, Facilities, Manufacturing, Validation, Engineering, Project Management, and Training Personnel

October 16 th, 2014 Benefits to the participants: What is GxP and why it is important Good Manufacturing Practices (GMP) Regulations & expectations Good Laboratories Practices (GLP) Regulations & expectations Good Clinical Practices (GCP) Regulations & expectations How to implement cgmp How to implement GLP How to implement GCP Role of QA, QC, Manufacturing, and Validation in GxP Who will be teaching? M. M. Chowdhury, ChE., PMP is an experienced Quality Assurance/ Validation Project Manager & Consultant/ Engineering & Validation Manager with over fourteen (14) years in the USA Pharmaceuticals, Medical & Biotech Industries. He managed and performed multiple equipment/system, utilities, facilities, computer, process and cleaning validation activities; and overseen Change Control, CAPA, Deviations, Calibration and Maintenance Programs, coordinated multiple USFDA and other regulators inspections. He also have worked in the areas of Validation Project Management, Remediation Projects, GMP Production Supports, QA, Global Outsourcing, Change Control System, GxP Compliance, Engineering, Technical Supports (Deviations, Investigations & CAPAs), Manufacturing, Technology Transfer/Scale Up, Supplier/Vendors/Contract Manufacturers/QA Audits and Quality Control. He has been an employee and consultant for multiple world-class USA pharmaceutical companies including Pfizer, Aventis-Sanofi, Johnson & Johnson, Dow Chemical, Élan Pharmaceuticals, CB Fleet Lab, AVI BioPharma and Cody Laboratories. Currently he supports Sanofi Pharmaceuticals as Quality & Validation Project Manager in Georgia, USA.

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