Description : Complying with GLP regulations can increase the cost of a laboratory up to 30%. Companies or employees either don't know exactly what GLP really means, or what procedures are required and how to implement GLP regulations. Lack of GLP knowledge is also an inspection issue as training plans should include basic GLP knowledge for everybody working in a GLP environment. Attend the seminar to get a good understanding on GLP regulations and get best practice guides and strategies for easy implementation.Areas Covered in the Session :FDA and International GLP regulations: 21 CFR Part 58, OECDExamples for FDA 483 inspectional observations and warning lettersObjectives, scope and concepts of GLP'sSpecial organizational requirementsResponsibilities: Management, Study director, QA, analystsSOP requirements: type, formats and enforcementGLP studies: preparation, conduct, documentationKey requirements for equipment, facilities reference material, peopleData generation and evaluation: raw data, intermediate results, final resultsRecords keeping: format, length of time, archiving and reprocessingStrategies for Multi-site GLP StudiesPreparing for FDA inspectionsWho Will Benefit:Everybody getting involved in GLP studiesLab Supervisors and managersQA managers and personnelGLP auditorsAnalystsConsultantsTeachersPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada Customer Support : 4169154458