Past Events (3,027)

January 12Wednesday

Analytical Instrument Qualification and System Validation

January 12, 2022 at 10am to January 13, 2022 at 5pm – online Analytical equipment should be qualified, and computer systems should be validated to demonstrate suitability for their intended use. To be acceptable to regulatory authorities, electronic records mu… Organized by ComplianceOnline | Type: seminae

January 11Tuesday

Clinical Research Revenue Cycle: Bridging Health Systems and Clinical Research

January 11, 2022 from 10am to 1pm – online Clinical research revenue cycle (CRRC) is an integral part of a clinical research portfolio. It is a complex environment that bridges a health systems revenue cycle with clinical research activities.… Organized by ComplianceOnline | Type: webinar
Pharmaceutical Water System: Design, Testing and Data ManagementIn this pharmaceutical water system webinar attendees will learn how to design, validate and maintain the new and existing water systems

January 11, 2022 from 10am to 1pm – online In this pharmaceutical water system webinar attendees will learn how to design, validate and maintain the new and existing water systems used in drug product manufacturing process. Different types of… Organized by Complianceonline | Type: webinar
Good Documentation Practice and Record Keeping Regulations (FDA & EMA)

January 11, 2022 from 10am to 1pm – online In this webinar, we will discuss the definition, purpose, importance of GDP, General rules of GDP, GDP as it applies to laboratory notebook documentation, US Pharmacopeia General Chapter <1029>… Organized by Complianceonline | Type: seminae
Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

January 11, 2022 at 9am to January 12, 2022 at 4pm – online This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirem… Organized by ComplianceOnline | Type: seminae

January 10Monday

Transfer of Analytical Methods according to USP <1224>

January 10, 2022 from 10am to 1pm – online In this analytical method transfer webinar attendees will learn the options available for the transfer of validated, non-compendial methods to a different site. In addition to current regulatory guid… Organized by ComplianceOnline | Type: webinar
Validation Sampling Plans

January 10, 2022 from 10am to 1pm – online This webinar will discuss setting up statistically justified sampling plans for process validation. Discussion will also involve using the sampling plan to set acceptance criteria for process validat… Organized by Complianceonline | Type: webinar
Supplier Management with the new Medical Device Regulation EU MDR 745/2017

January 10, 2022 from 7am to 10pm – online In this webinar, learn how to implement the changes required by the new regulation EU MDR 745/2017 in your current quality management system in a simple and quick way. The information in this course… Organized by Complianceonline | Type: webinar

December 16Thursday

Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines

December 16, 2021 at 10am to December 17, 2021 at 5pm – online Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect the regulated industry to h… Organized by ComplianceOnline | Type: seminae
Lifecycle Management of Analytical Methods and Procedures according to new USP and ICH Guidelines

December 16, 2021 at 10am to December 17, 2021 at 5pm – online Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect the regulated industry to h… Organized by Complianceonline | Type: webinar