This food safety compliance training will provide a comprehensive understanding of FDA’s new Food Safety Law and show how to comply with the new set of requirements for recordkeeping, hazard analysis, supplier verification, etc

This webinar on pharmaceutical stability program will discuss the types of CMC changes in the life cycle of a pharmaceutical product and how it affects the stability program.

This webinar on FDA social media regulations will discuss the best practices utilized by medical device, drug and other FDA and FTC regulated industries when using social media channels, i.e., Web 2.0, like Facebook, Twitter, YouTube and LinkedIn to promote products.

This training will review a number of actions exporters should take to protect their patents (inventions), trademarks (words and symbols that identify products) and copyrights (works of art or authorship) in foreign markets.

This webinar on bioequivalence will use a case study approach to explore the regulatory issues relevant to the approval of medications designed to be bioequivalent with already-marketed drugs. It covers current regulatory definitions, requirements and relative exceptions to bioequivalency and therapeutic equivalency.

This training on accounts payable (AP) automation will highlight its emerging market specifically the invoice side of the process and it will also discuss the special considerations for a move towards invoice automation.

This OSHA Recordkeeping training will address the key concepts in understanding the OSHA recordkeeping analysis through recent OSHA Interpretation Letters. This training will include hypothetical fact scenarios that present common recordkeeping issues encountered by facility record keepers.

This webinar on the role of lab data in drug development and clinical research safety monitoring will provide tips on how to analyze lab data to determine adverse events.

This webinar will discuss the disclosure requirements for clinical investigators under the Sunshine Act. It will discuss the details of the processes; provide templates for reporting formats; and timelines for reporting.

This laboratory compliance training will explain how to qualify and validate vendors for reagents in a GLP/GMP laboratory.