Wednesday, January 12, 2022

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
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
Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance

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
SaaS/Cloud Risk-Based Validation With Time-Saving Templates

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
21 CFR Part 111 - Master Manufacturing Records and Batch Production Records

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
Human Error Reduction Techniques for Floor Supervisors

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
Calculations for Process and Product Capability

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