Data Integrity 2016 - Advanced Auditing for Data Integrity - By Compliance Global Inc

Overview:
Any successful records management plan will start with a benchmark assessment of your current state followed by a data integrity audit.
Why Should You Attend:
Where are your records, what are the formats, how are they being tagged and classified, what kinds of policies are you applying to management and how well and consistently are you enforcing those policies?
Areas Covered in this Webinar:
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.
Learning Objectives:
Learn how to establish a baseline
Learn how to apply consistent meta tags to all documents
Learn how to apply consistent policies to all records
Learn how to achieve a best practice level of compliance
Learn how to centralize management and eliminate silos
Learn how to reduce compliance and e-discovery risks
Learn how to build a better business equipment case
Who Will Benefit:
Senior Quality Managers
Quality Professionals
Regulatory Professionals
Compliance Professionals
Production Supervisors
Validation Engineers
Manufacturing Engineers
Production Engineers
Design Engineers
Process Owners
Quality Engineers
Quality Auditors
Document Control Specialists
For more information, please visit : https://complianceglobal.us/product/700440/JoyMcEl...
Email: support-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Level:
Intermediate
Speaker Profile:
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 of 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.