Labcompliance On-line Audio Seminar
This seminar has been recorded and is
available on CD and for instant download. All reference material as
listed below and more is available on a special seminar website. The
website is regularly updated with most recent information. In case
there are questions related to the topic, they can be submitted
through a web form and will be answered by the speaker. For ordering
info
click here)
On-line Audio Seminar 217
IT Infrastructure and
Network Qualification
Introduction and
Strategies for Compliance and System Uptime
Recorded, Available on
Demand

Federal laws and regulations mandate to put controls and
measures on a company network to ensure security and data integrity. Examples
are 21 CFR Part 11, Sarbanes-Oxley Act, and HIPAA. With this legislation IT
infrastructure and network qualification and compliance become a much more
recognizable issue at higher levels of management. However currently there is no
official guideline and the situation is similar to what happened with computer
validation in early 90's and with early Part 11 issues. Until there will be an
industry wide accepted approach companies either waste valuable resources
because doing too much or take a risk to fail inspections because not doing
enough or doing it wrong. With FDA's renewed focus on computer validation and IT
systems, industry is looking for advice on how to comply for networks and
infrastructure.
Key Questions are:
- What does network compliance mean?
- Is there an official guidelines from the
FDA?
- What do inspectors ask and what do they
want to see?
- What is the approach of the GAMP5 and
GAMP/ISPE Good
Practices Guides?
- What does the approach of the IVT
proposed standard?
- Should networks comply with 21 CFR Part
11?
- What about other legislation such as
Sarbanes-Oxley and HIPAA?
- We validate the application running on
the network, so we know that it works, why should we qualify the
infrastructure?
- How much testing is enough: should we
test each network component, like switches, routers and servers?
- How to verify accuracy and integrity of
file transmissions?
- How to qualify PC clients, servers and
data centers?
- I have multiple clients with the same
configuration, should I qualify/validate all of them?
- We have an existing network, where and
how should we start?
- How to deal with security patches?
- Our network changes so often, how can I
keep it in a validated state?
How does the this audio seminar help:
Answers will be presented by Dr. Ludwig Huber
in a new interactive audio seminar. During the seminar, the speaker
will present strategies and give practical recommendations. After
the seminar, an extensive list of reference material like SOPs,
templates and examples will help immediate and cost effective
implementation.
During the interactive presentation you learn
about:
- Laws, regulations and guidelines- 21 CFR
Part 11, HIPAA, Sarbanes-Oxley
- The FDA Industry Guide: Cybersecurity for
Networked Medical Devices
- The GAMP/ISPE Good Practices Guide
- The IVT proposed NIQ standard
- Principles of network infrastructure
qualification
- Compliance concepts for infrastructure
vs. networked systems
- Configuration management and change
control as the most important network qualification steps
- Qualification of PC clients, servers,
data centers
- What and how much to test with the risk
based cost/benefits in mind: network components, servers, PC
clients, applications, initial vs. on-going testing
- How to ensure highest system uptime with
on-line monitoring tools
- Documentation requirements
- Going through a life inspection
- Software tools for infrastructure
qualification
And for easy and instant implementation:
download 15+ documents from special seminar website
- Example: Network Infrastructure
Qualification Plan
- SOP: Qualification of PC Clients
- SOP: Qualification of Data Centers
- SOP: Qualification of Servers
- SOP: Handling Security Patches
- SOP: Testing File Integrity of E-Mail
Attachments
- SOP: Using the Internet in Regulated
Environments
- SOP: Change Control for Networks and
Systems - Planned Changes
- SOP: Change Control for Networks and
Systems - Unplanned Changes
- Gap Analysis/Worksheet: Network
Infrastructure Qualification and System Validation
- SOP: Risk Based Qualification of Network
Infrastructure
- SOP: Development and Maintenance of Test
Scripts for Equipment Hardware&Software
- IVT Standard: Network Infrastructure
Qualification
- Article published in Biopharm:
Qualification of Network Infrastructure and Validation of
systems
- Example: Testing Authorized System Access
- Template: Network Infrastructure and
System Identification
- FDA Inspection Report: Five page FDA
inspectional inspectional observation and several warning
letters with deviations related to network infrastructure
- NIST Guidelines related to IT Security
- Related laws and regulations
Who should attend?
- IT managers and personnel
- Everybody responsible for FDA compliance
of computer systems
- Managers from purchasing, documentation
and operations
- All users of computer systems used in
regulated environments
- QA managers and personnel
- GLP/GMP/GCP auditors
- Consultants
- Teachers
How to order
Pick one of the options in the table that fits your needs.
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Recorded seminar -
Web Download
- Multiple persons - single site
- Learn at your desk, meet in a seminar or conference
room or share the audio file and reference material at your site.
- Order includes all reference material.
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US$ 399.-

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Recorded seminar -
CD
- Get the CD in your mail
- Order includes all reference material.
|
US$ 399.-

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Special offer for
Labcompliance Usersclub Members
Recorded Seminar- CD or Web download.
- Order includes all reference material.
- for Usersclub information and registration,
click here
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US$ 299.-

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About audio seminars

Online audio seminars are
presented over the phone. During the live presentation attendees
can:
- Study the printed slide material
- Watch the slides on a computer
- Watch the slides on a video screen in a
seminar room
- Ask questions through email and web form
About Dr. Ludwig Huber
Dr. Ludwig Huber is the author of the Labcompliance
Newsletter. Since over 10 he has been conducting over 150 web and audio or video
based seminars. He is chief advisor for FDA compliance at Labcompliance.
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Dr. Ludwig Huber is a frequent presenter
at IVT conferences and has been awarded as the 'Presenter of
the Year' out of 170 speakers. This photo is from IVT's
conference on Network Qualification with Ludwig Huber as
plenary speaker. |
Dr. Huber has published several books related
to validation and compliance, for example: Validation of
Computerized Analytical and Networked Systems. He was or still is a
member of several committees, e.g., of the GAMP Special interest
group (SIG) on Laboratory Computers, PDA Part 11 task force, IVT
task force on network infrastructure qualification and the European
Compliance Academy. He frequently visits FDA in Rockville, VA, and
participates in panel discussions with FDA professionals. For more
information,
click here.