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All pharmaceutical Events (32)
July 24Tuesday
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ICH Q10; moving from GMPs to a Pharmaceutical Quality System - Webinar By ComplianceOnline
July 24, 2012 from 10am to 11:30am – Online Event This ICH Q10 training /webinar will discuss the evolution and interpretation of the pharmaceutical GMPs as a quality control regulation to the Quality Assurance emphasis of the Pharmaceutical Quality… Organized by Referral | Type: pharmaceutical, training
August 20Monday
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Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA
August 20, 2012 from 10am to 11:30am – Online Event This 90 minute interactive webinar will review the dietary supplement regulations and discuss how to verify that your products are compliant, while citing differences with food and drug regulations.… Organized by Referral | Type: pharmaceutical, training
May 2Thursday
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Effective and Compliant Change Control Management - Before, During and After Validation - Webinar By GlobalCompliancePanel
May 2, 2013 from 10am to 11:30am – Online Training Overview: There is a need to implement an adequate formal level of change control during engineering projects (referred to as an Engineering Change Control) after the approval of the equipment/system… Organized by John Robinson | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 7Tuesday
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Common Problems with Software Validation Processes - Webinar By GlobalCompliancePanel
May 7, 2013 from 10am to 11:30am – United States Overview: This webinar covers the fundamentals of 21 CFR Part 11, software validation, and computer system validation. It provides details for company compliance including GAMP, qualification, and va… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 8Wednesday
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CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations - Webinar By GlobalCompliancePanel
May 8, 2013 from 10am to 11am – Online Training Overview: Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations, and hazard analysis / risk management and mitiga… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
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Medical Device Design Control - Webinar By GlobalCompliancePanel
May 8, 2013 from 10am to 11am – Online Training Overview: Understanding, interpreting, and implementing design control requirements in a holistic manner can significantly expedite the regulatory processes, bringing innovative medical products to t… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
May 9Thursday
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edical Device Postmarketing Vigilance Reporting: Update and Expectations for Manufacturers - Webinar By GlobalCompliancePanel
May 9, 2013 from 10am to 11am – Online Training Overview: Major postmarketing vigilance revisions are now in force. A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) came into force on January 1, 2008. Pro… Organized by GlobalCompliancePanel | Type: webinar, healthcare, medical, device, pharmaceutical, clinical
December 12Thursday
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Why and How - Verification of Compendial Methods - USP <1226>
December 12, 2013 from 10am to 11:30am – Online Event This USP <1226> webinar training will discuss the requirements of USP <1226>, what are FDA expectations related to method verification. Why Should You Attend: Analytics continues to be a… Organized by ComplianceOnline | Type: pharmaceutical
January 9Thursday
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Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions: One and a Half-day In-person Seminar
January 9, 2014 at 8:30am to January 10, 2014 at 12:30pm – Residence Inn San Diego Downtown Course Description: Every company regulated by the U.S. FDA establishes procedures, practices and an internal monitoring system all designed to both meet the regulations and manage inspections. Howev… Organized by ComplianceOnline | Type: biotech, and, pharmaceutical
January 15Wednesday
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Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina): 2-day In-person Seminar
January 15, 2014 at 8:30am to January 16, 2014 at 4:30pm – Grand Hyatt San Francisco, CA Course Description: This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registr… Organized by ComplianceOnline | Type: biotech, and, pharmaceutical
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