Records Management Applied To FDA Regulatory Compliance
November 28, 2012 - Palo Alto CA US
This webinar on FDA compliant records management will discuss strategies and tools, other than software solutions, for short and long-term archiving of records, while taking into account technology changes in records management. Why Should You Attend: The FDA and other regulatory organizations have short-term, often vague, requirements for retaining records. It is common practice for organizations to keep every document that could possibly be associated with the filing of a drug marketing application and subsequent clinical trials and manufacturing. Because of the increased volume of information being retained, organizations face huge challenges in finding and retrieving specific records that were needed for audits or filings. In this session, the speaker will show how you can build retention schedules based on your business needs. We will present tools, other than software solutions, that will help you ensure that all essential records are captured, protected and disposed of when they have no intrinsic value to the organization. The speaker will also discuss strategies for short and long-term archiving of records, while taking into account technology changes in records management.