Over two days in which nearly 12,000 visitors came through its doors, the expo served to set up 1,514 meetings between entrepreneurs and investors as well as bringing together 256 experts in business strategy, internationalisation, financing, marketing, innovation and sales.

This training on data security will provide the tools to design and implement effective IT control structures and audit programs to help comply with the current data privacy and confidentiality regulations.

1 Million Cups Kansas City: Slik Hound and Phony Invoices

This training on fraud awareness program will discuss recent history and profile of fraud cases and will help attendees understand specific processes and techniques needed to be effective when providing assistance on fraud issues.

This webinar on Medical Device Reporting (MDR) will cover FDA requirements for importers, manufacturers and hospitals to report medical device adverse events. It will discuss current policies and guidances for Medical Device Reporting and provide update on upcoming regulations.

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 prepare you and your company for tougher US FDA cGMP compliance audits.

Behind every successful e-seed entrepreneur is a trusted mentor and guide. Now, we’re bringing the program that launched hundreds of new businesses right to you.

Each hack night, anyone who wants to lead a project can write their idea on the whiteboard, and spend 5-10 minutes describing what they want to work on. Anyone attending can join up with any of the leaders, and we'll break into 4-5 groups each working on a cool, interesting problem.

This training will teach you how to prepare for a medical staff professional review adverse action hearing, including what steps are necessary to afford the respondent practitioner due process.

This pharmaceutical water systems webinar training will discuss what you should do when your monitoring data tells you that you may have a significant biofilm problem. It covers how to verify that the data and your interpretation of the data are correct, as well as the location of the problem which gives you clues as to what caused the problem and its impact on manufacturing and product.