BEGIN:VCALENDAR PRODID:-//github.com/rianjs/ical.net//NONSGML ical.net 4.0//EN VERSION:2.0 BEGIN:VEVENT DESCRIPTION:Good Manufacturing Practices (GMP) describe the requirements f or manufacturing drug product in each country or region and cover areas s uch as facility design and sanitation\, product testing\, product identif ication\, equipment\, packaging\, warehousing and distribution\, and reco rdkeeping. These requirements include the required education\, training a nd experience for employees whose activities affect the quality of drug p roducts. Among those educational requirements are a course in Introductor y GMP upon employment at a pharmaceutical company\, and annual refresher GMP training.\n\nThe goal of this seminar is to enable you to:\n\n\nDemon strate a basic knowledge of GMP requirements\nInterpret these requirement s for your day-to-day operations\nAvoid the negative consequences of nonc ompliance\nInstill a culture of compliance in your organization\n\nThe su bject of introductory GMP includes a discussion of the pivotal events tha t have shaped US laws on food\, drugs and cosmetics\; use of the terms GM P and cGMP (Current Good Manufacturing Practices)\; key sections in the U S Code of Federal Regulations that impact drug manufacture\; and how an o rganization can remain compliant with these regulations in their day-to-d ay operations.\n\n \;\n\nWhy should you attend:\nThe laws that govern Good Manufacturing Practices (GMP) are a cornerstone of pharmaceutical p roduction. Still\, many companies fall short of the requirements that are written into US\, UK\, European and other laws\, which can have disastro us consequences for patient health and a company's reputation\, not to me ntion the resultant losses in revenue due to fines\, declining sales and withdrawal of products from the market. It is expected that all employees who are involved in pharmaceutical production will attend GMP-related tr aining on a regular basis.\n\n \;\n\nAreas Covered :\n\nFood and drug oversight\nPivotal events that shaped laws in US and scope of FDA action s\nGMP vs. cGMP\nConsequences of noncompliance\nBuilding a culture of com pliance\nEmphasis on education and decision-making\nTraining\, memory ret ention\, and accountability\nAvoiding over-reliance on metrics\nRecent tr ends in GMP enforcement and lessons learned\n\nWho will Benefit:\nThis co urse will be of benefit to anyone whose responsibilities fall under the u mbrella of manufacturing\, packaging or distribution of pharmaceutical pr oducts (e.g.\, Quality Assurance\, Packaging\, Operations\, Planning).\n DTEND:20260417T140000 DTSTAMP:20260417T061521Z DTSTART:20260416T080000 LOCATION:\, SEQUENCE:0 SUMMARY:Good Manufacturing Practices (GMP) describe the requirements for m anufacturing drug product in each country or region and cover areas such as facil... UID:f1e7d472-96cb-4f0b-84d8-e0b5f86cab06 END:VEVENT END:VCALENDAR