Past Events (3,027)

Raw Material Requirements

February 28, 2022 at 10am to March 1, 2022 at 4pm – online Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology produ… Organized by ComplianceOnline | Type: seminae

Dietary Supplements - Regulatory Compliance Requirements

February 24, 2022 from 10am to 1pm – online This training will review the dietary supplement regulations in the USA and explain how to verify that your products are compliant with the most recent regulations and provisions. It covers the FDA r… Organized by ComplianceOnline | Type: webinar
Human Errors in GMP Manufacturing and Laboratory Processes Identification

February 24, 2022 from 10am to 1pm – online This instructor-led live training webinar will discuss regulatory requirements for detecting, correcting and preventing human errors in manufacturing and laboratory environments as well as developing… Organized by ComplianceOnline | Type: webinar
Design Control for Medical Devices Including Verification/Validation

February 24, 2022 from 10am to 1pm – online Overview of design control for medical devices with and emphasis on verification and validation of design inputs. Webinar will cover basic regulations regarding verification/validation of inputs, tra… Organized by ComplianceOnline | Type: webinar
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations

February 24, 2022 at 7:30am to February 25, 2022 at 1:30pm – online The globalization of the pharmaceutical supply chain has resulted in the increased use of Contract Manufacturing Organizations (CMOs). The use of CMOs provides many benefits; however, it also present… Organized by ComplianceOnline | Type: seminae

Supplier Management: Challenges and Opportunities

February 23, 2022 from 10am to 1pm – online Attend this webinar to learn the QSR and ISO requirements for supplier evaluation, including defining the types of suppliers that require evaluation, including “critical” suppliers and outsourced pro… Organized by Complianceonline | Type: webinar
Analytical Method Validation and Transfer

February 23, 2022 from 10am to 1pm – online This course will provide a thorough review of regulatory guidelines on method validation and transfer. It provides guidance on how to perform QC analytical test method validations and transfers. Why… Organized by ComplianceOnline | Type: webinar

Structuring and Conducting Risk-Based Internal cGMP Compliance Audits

February 22, 2022 from 10am to 1pm – online This training will evaluate the chief areas of an FDA cGMP compliance audit and help you understand the actual and anticipated changes in emphasis based on this new regulatory climate. It will prepar… Organized by ComplianceOnline | Type: webinar
Structuring and Conducting Risk-Based Internal cGMP Compliance Audits

February 22, 2022 from 10am to 1pm – online This training will evaluate the chief areas of an FDA cGMP compliance audit and help you understand the actual and anticipated changes in emphasis based on this new regulatory climate. It will prepar… Organized by ComplianceOnline | Type: pharma

21 CFR Part 111 - Current FDA 483 Observations and Warning Letters Review

February 18, 2022 from 10am to 1pm – online The FDA inspects facilities, online marketing collateral and physical products to determine compliance with the 21 CFR Part 111 dietary supplement regulations. It is very helpful to review their obse… Organized by ComplianceOnline | Type: webinar