Events Happening Now
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems
(www.complianceonline.com) – All pharmaceutical, biologics, and medical device facilities are likely to have high purity water systems. In spite of this purity, microorganisms can flourish within these systems and lead ... Read More
Events Happening Later
Auditing and Administrating Human Resource Policies and Practices
(www.complianceonline.com) – This two-day seminar provides information and techniques for handling human resources practices legally and effectively. Beginning with an overall audit of human resources practices, this se... Read More
Accelerating Bioassay Transfer in a GMP Environment
(www.complianceonline.com) – This Bioassays webinar will systematically outline the steps needed to successfully transfer validated biological assays between GMP/GLP labs and also acquire non-validated assays for GMP/GL... Read More
Understanding Design Controls for Medical Devices
(www.complianceonline.com) – This webinar will cover the basics of design controls for medical devices, and provide recommendations for implementation of a compliant design control system. Read More
Submission Documentation for Sterilization Process Validation - A Comprehensive View of Content for an Approvable CMC Section
(www.complianceonline.com) – In this sterility assurance documentation webinar, you will learn specifically what information is required in sterility assurance documentation for injectable drug products and how to prese... Read More
The Regulation of Pet Food in the United States
(www.complianceonline.com) – This 90-minute training will provide an introduction to FDA’s rules governing pet food product development and formulation, manufacturing, labeling; and marketing and promotion. Read More
Validation of Analytical Procedures for Use in the Pharmaceutical Industry
(www.complianceonline.com) – This 6-hr virtual seminar will review analytical procedures used in assessing quality, safety and efficacy of drug products. It will cover the ICH and USP guidelines for procedure validation... Read More
Leaping into Lab: Everything about Waived Testing
(complianceonline.com) – This CLIA Webinar training will feature an in-depth look at CLIA Waived Testing. It will present the rules and regulations as well as the pros and cons of testing using Waived methods. Wh... Read More
What’s New in HR Auditing
(www.complianceonline.com) – This HR Audit training will help you assess your organization's risks and discusses the use of HR audits as a continuous audit process that strengths internal controls, provides assuran... Read More
International Trade Finance Payment Methods
(www.complianceonline.com) – This 90-minute will help exporters and importers understand the three international trade finance methods of payment; to include Letters of Credit, Documentary Collections and Open Account; ... Read More
Child Support: Complete and In-Depth
(www.complianceonline.com) – This 3-hr virtual seminar on child support regulations will focus on federal and state requirements to compliantly and effectively handle child support withholding orders. Why Should You ... Read More
Global Data Transfer Solutions – Complying with EU Laws & Regulations
(www.complianceonline.com) – This webinar will help you understand the EU data transfer regime and the significant differences within the EU member states in relation to the way in which data transfers are permitted fro... Read More
OSHA Recordkeeping: Recent Recordkeeping Interpretations
(www.complianceonline.com) – This 90-minute OSHA Recordkeeping training class will incorporate the lessons learned from OSHA’s recent Interpretation Letters into the existing OSHA recordkeeping analysis as well as OSH... Read More
Defending Against an OFAC Investigation
(www.complianceonline.com) – This webinar on Defending Against OFAC Investigations is designed to teach participants to successfully navigate the OFAC enforcement process and reduce any OFAC penalties. Read More
Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results
(www.complianceonline.com) – This 2-hr Dissolution Instrument Qualification webinar will discuss recent FDA requirements for dissolution instrument qualification and provide practical suggestions to avoid pitfalls in pe... Read More
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials
(www.complianceonline.com) – This 90-minute webinar will provide an overview of regulatory management for clinical trials. It will discuss key regulatory aspects of a clinical project such as clinical protocol managemen... Read More
DMR & DHR - What Is Really Required
(www.complianceonline.com) – This 90-minute training will discuss the FDA's QSR requirements for a Device Master Record (DMR) and how you can use it to build your Device History Record (DHR). Read More
Solutions to the Challenges of Phase I and FIM Studies in Today’s World
(www.complianceonline.com) – This 90-minute webinar will help you identify the challenges in Phase I and FIM studies and present solutions on how to overcome these challenges. Why Should You Attend: As need for mo... Read More
South Korea: Navigating the Regulatory and Clinical Trial Environment
(www.complianceonline.com) – This 6-hr virtual seminar will focus on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products in South Korea. Read More
SSAE 16 (formally known as SAS70), SOC1 to SOC 3 Reporting Demystified
(www.complianceonline.com) – In this 90-minute training you will learn more about SSAE 16 (formally known as SAS 70), SOC 1, SOC 2 and SOC 3 reporting, how to choose the right report for your organization and how to get... Read More
