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FDA 21 CFR Part 11
Presented By 247compliance
Thursday, October 24th at 1:00pm EST
Online sale ends: 10/24/19 at 12:00pm EST
2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 19702
Online, DE 19702
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Willi Ramseier

This webinar will show you that there is no sense in tackling the ‘keeping’ of the records, by trying to follow Part 11, because the record requirements must come from the parties who provide, create, or change the records.

If you are part of the process of ‘Collecting’ (e.g.: from study nurse to x-ray specialist), ‘Using’ (e.g.: from sponsor to report programmer, or statistician), or ‘Keeping’ (e.g.: from coder, software provider, to server and backup specialist), then this webinar will answer the questions: of how important your part is in this process, and how you can help the company safe resources and be compliant.

If an effort is made to collect research-, study-, patient- or other important records, they should be kept safe, in a controlled and organized way. That way is defined by the requirements.

The cost of lost data/records can be staggering; also, the mishandling of records or lack of safekeeping. Withdrawing or the wish of deleting could be a big problem too.

It is not only about data or records but different samples as well which must be managed in the same way.

There is never ‘one fits all’ but the FDA’s 21 CFR Part 11 is still perfectly usable after many years. The main reason for that is, that it points to the requirements of predicate rules.

You have to provide an assured level of quality right from the beginning of the process (collecting records); that at the end the inspector, with the Part 11 in hand, will find no negative observations.

Overview and Definitions
The reasons why only talking about records or data is not enough
The relationship between the owner or provider, the collector or user, and the keeper
The forgotten loop
Common mistakes and today's problems (including ‘Big Data’)
Best practices or the ideal process
Course Level - Overview of the relationship between the groups which take part in the process of providing, using and safekeeping of records and samples. The fundamental importance of requirements; who needs to provide them, and what they are used for.

Clinical Operations Professionals (from study nurse to x-ray specialist)
Clinical Quality Assurance Professionals
Data Management Professionals
Clinical Investigators and Clinical Investigator Site Staff
Sponsors Clinical Study Groups
Clinical Trial Statisticians and Statistical Programmers
Clinical Electronic Systems Developers (also Big Data)
Service Providers (for saving and maintaining any samples of importance)

Willi Ramseier is the pragmatic system thinker, project management skills, risk management know-how, expertise in CAPA system and QMS (quality management system), a consultant for general quality issues (especially for start-ups)

For more detail please click on this below link:
Email: support@247compliance.com
Tel: +1-(510)-868-1040

Presented By

1:00pm to 2:00pm
Doors open at 1:00pm

General Admission: $199.00

All Ages

247compliance.com<br> 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 19702<br> Online, 19702


FDA Compliance


Tuesday, October 22nd

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