Why Should You Attend:
This webinar will help attendees learn how to apply consistent meta tags and policies to all documents and records. It will also teach how to reduce compliance and e-discovery risks.
This webinar is designed for people tasked with performing audits for their organizations for data integrity. It is also for those tasked with records management. This includes individuals that have Quality Management Systems responsibilities for making general improvements in their organization’s performance specifically related to equipment that produces and stores data, processes and documentation.
Areas Covered in the Webinar:
Applying consistent meta tags to all documents
Applying consistent policies to all records
Achieving a best practice level of compliance
Centralizing management and eliminating silos
Reduce compliance and e-discovery risks
Building a better business case
This webinar will help attendees learn how to apply consistent meta tags and policies to all documents and records. It will also teach how to reduce compliance and e-discovery risks.
This webinar is designed for people tasked with performing audits for their organizations for data integrity. It is also for those tasked with records management. This includes individuals that have Quality Management Systems responsibilities for making general improvements in their organization’s performance specifically related to equipment that produces and stores data, processes and documentation.
Areas Covered in the Webinar:
Applying consistent meta tags to all documents
Applying consistent policies to all records
Achieving a best practice level of compliance
Centralizing management and eliminating silos
Reduce compliance and e-discovery risks
Building a better business case
Speakers
Upon earning a degree in Zoology at North Carolina State University, Joy McElroy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing environmental monitoring and sterility testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their quality control lab. In 1998, Ms. McElroy moved to Wyeth Lederle and worked in quality assurance, performing GMP compliance audits, batch record reviews, and holding annual GMP training for new employees. After working in quality assurance for a few years, she moved into equipment qualification and cleaning validation at Mallinckrodt.With over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of quality assurance, process and cleaning validation, equipment qualification, sterilization, and GMP compliance auditing. Her knowledge, experience, and strong work ethic have made her a highly sought-after engineer in both the pharmaceutical and biotech industries.
In 2013, Ms. McElroy started her own company, Maynard Consulting Company, which provides top engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients across the United States, Canada, and the world.
