HIPAA Compliance for Electronic Records
Instructor:
David Nettleton
Product ID: 704422
- Duration: 75 Min
Why Should You Attend:
This webinar will detail the regulations for electronic records related to Health Insurance Portability and Accountability Act (HIPAA) patient medical data. What makes this session unique is the understanding of how Part 11 and HIPAA industry standards have evolved together thereby reinforcing each other.
Areas Covered in the Webinar:
- Evolution of 21 CFR Part 11 to the latest HIPAA regulations for patient medical records.
- Specifics of the regulations, 45 CFR Parts 160, 162, and 164 the HIPAA electronic record security regulation that became effective in 2005.
- How to configure your system and processes for compliance.
- Which data and systems are subject to HIPAA
- What HIPAA means, not just what it says?
- Examine the regulatory requirements for the four primary areas of compliance: SOPs, software product features, infrastructure qualification, and validation documentation.
- Evaluate the regulatory requirements for security, data transfer, audit trails, electronic signatures, digital pens, and biometric signatures.
- SOPs required for the IT infrastructure.
- Reduce validation resources by using easy to understand fill-in-the-blank validation documents.
Who Will Benefit:
- Computer system users
- IT personnel
- QA/QC personnel
- Managers
- Executives
Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, software validation, and computer system validation. He is involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications.
He has completed more than 260 mission critical laboratory, clinical, and manufacturing software implementation projects. His most popular book is Risk Based Software Validation - Ten easy Steps, which provides fill-in-the-blank templates for completing a COTS software validation project.
More Training By Experts
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- Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance
- 10-Step Risk Based Computer System Validation for SaaS/Cloud/Local Hosting
- Use Risk Assessment to Reduce Validation Time for 21 CFR Part 11
- Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR
Refund Policy
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
