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January 14, 2022 from 10am to 1pm – online Data Integrity has been the subject of increasing scrutiny during pharmaceutical regulatory inspections in recent years. Chromatographic data systems have received particular attention because of the… Organized by Complianceonline | Type: webinar
January 14, 2022 from 10am to 1pm – online Corporations are facing more risks in the expanded environment of business. This webinar will provide auditors and audit management with advanced approaches to risk management and internal risk asses… Organized by Complianceonline | Type: webinar
January 13, 2022 from 10am to 1pm – online Dietary Supplement companies must ensure that any product claims they make are “truthful and not misleading” under FDA and FTC regulations. To meet these standards, the FTC has stated that claims mus… Organized by ComplianceOnline | Type: webinar
January 13, 2022 from 10am to 1pm – online This course will look at the new FDA direction and other programs aimed at transforming food safety in 2022 and beyond, including how to manage #483 violations for non-compliances. Why Should You At… Organized by Complianceonline | Type: webinar
January 13, 2022 at 8am to January 14, 2022 at 2pm – online The average cost of a Notice of Proposed Penalty is estimated at US $150,000 including the penalty itself and the added costs for consultants, personnel, remediation of legacy records, etc. Complianc… Organized by ComplianceOnline | Type: seminae
January 12, 2022 from 10am to 1pm – online Attendees of this webinar will learn specific concepts and formulas commonly used to measure the ability of a process to produce output within customers’ specification limits. The focus of this webin… Organized by Complianceonline | Type: webinar
January 12, 2022 from 10am to 1pm – online Attend this course to gain practical approaches for supervision on the floor, strategies to get your group in sync and approach issues in GMP related environments by using a specific methodology to c… Organized by Complianceonline | Type: webinar
January 12, 2022 from 10am to 1pm – online The single most critical document in an FDA inspection is the master manufacturing record and associated batch production record. While the 21 CFR Part 111 regulations have a checklist of elements th… Organized by Complianceonline | Type: webinar
January 12, 2022 from 10am to 1pm – online This 21 CFR Part 11 compliance training will guide you through the requirements of Part 11 and will also explain its 3 primary areas: SOPs, product features and validation (10 step risk based approac… Organized by ComplianceOnline | Type: webinar
January 12, 2022 from 10am to 1pm – online FDA’s recent focus on data integrity during computer system validation inspections and audits has brought this issue to the forefront of importance for compliance of systems used in regulated industr… Organized by Complianceonline | Type: webinar
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