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MEDICAL SPECIALTIES ...

Which data and systems are subject to Part 11

From Tuesday, January, 16, 2018 to Tuesday, January, 16, 2018 in CA
Starting from:10:00
Concerned sectors: Biotechnology -Medical Informatics -
DESCRIPTION
Overview: 
This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach.

Areas Covered in the Session:
Which data and systems are subject to Part 11
What Part 11 means to you, not just what it says in the regulation
Avoid 483 and Warning Letters
Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation
Ensure data integrity, security, and protect intellectual property

Who Will Benefit:
IT
QA
QC
Laboratory Staff
Managers
GMP, GCP, GLP Professionals

Speaker Profile:
Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
PUBLIC, SECTORS, ACCREDITATION
Accreditations: 0
Concerned Public: General public
Attendance: International
Visitors/Participants: 100
Speakers: 1
Exhibitor: n.c
Event Type: Online Conference
Major Sector: BIOTECHNOLOGY
Concerned sectors: Biotechnology -Medical Informatics -
ORGANIZER / ADVERTISER

COMPLIANCE4ALL
161 Mission Falls Lane, Suite 216,
94539 Fremont
UNITED STATES

COMMENT
REFERENCE
Congress, conferences or medical training REF #28-7700
Which data and systems are subject to Part 11
Published on congres-medical.com on:2017-11-14 13:45:18
Congress, conferences or medical training in BIOTECHNOLOGY
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