Compliance2go

Medical Records serve many purposes in patient care so any revisions should only be done according to certain procedures and rules, in order to avoid serious compliance consequences.

This interactive webinar explains how to configure and validate a GxP compliant spreadsheet application to avoid FDA 483s.

Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of

This course will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data,

Understanding the potential risks and benefits to your clinical development program is essential if you plan to implement centralized monitoring as described in the recently released FDA Guidance: Oversight of Clinical Investigations —

This 90 minute webinar will help you gain a detailed overview of ICH GMPs and the nuances and differences between requirements in the US, EU and Japan. It will help prepare you for regulatory inspections in these countries.

This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly. Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory

This course will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data,

Enforcement of HIPAA regulations is being stepped up and new fines and penalties make being ready for an audit in advance essential.

Summary "Attendees will receive a complimentary e-book of " How to write standard operating procedures and work Instructions", published by the Instructor in 2010.The e-book will be send out to attendees after the webinar.