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There is no doubt that data integrity is the current and future inspection focus of all regulatory heath care agencies. More than 50% inspection reports such as 483's and Warning Letters quote data integrity as deviations from GxP regulations.

This new 2-day course provides the regulatory background and guides attendees through the complete record lifecycle from data entry or acquisition through evaluation, reporting, archiving and retrieval. It also helps to fully understand not only the text but also the meaning of related regulations such as FDA's Part 11 and the EU/PICS Annex 11.

The 2-day course not only ensures a full understanding of the regulations and guidelines for raw data and other records but also provides templates and examples to develop inspection ready documentation. Interactive exercises will be dispersed into and between the presentations. About 50% of the total time will be dedicated to practical sessions. Here attendees work in small groups on case studies and prepare the answers using prepared fill-in templates. After the course a large variety of tools such as SOPs, validation examples and checklists will be readily available on a dedicated website that can be used to easily implement what they have learned in the course.

Learning Objectives:
Attendees will:

Understand what data integrity is and why it is so important for public health
Learn why there are so many data integrity issues
Learn about the FDA/EU/PICS/MHRA/WHO requirements for data integrity
Understand how to define and archive raw data from hybrid systems: electronic vs. paper
Be able to specify and validate Part 11 compliant software functionality

Who will Benefit:
QA managers and personnel
Laboratory managers and supervisors
Production managers and supervisors
IT/IS managers and system administrators
Software developers
Regulatory affairs
Training departments

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

Contact the event managers listed below for more information about how you can participate at the Data Integrity: FDA/EU Requirements and Implementation: 2-Day Workshop by Dr. Huber.

All information in Events In America is deemed to be accurate at the time we add it, and we take steps to verify all details and update our records when new information is provided, but as people, events and circumstances change, we caution users to independently confirm all information. and Events In America LLC make no guarantee of accuracy and assume no liability for inaccurate information.

Conference/Event Dates: 07/05/2016 - 07/06/2016
Conference/Event Hours: 8:30 AM - 4.30 PM
Classification: B2B
Primary Industry: Sciences
Other Industries: Business, Sciences
Estimated Attendance: 30
Cost to Attend: One Registration - $1899
Audience: QA managers and personnel
Laboratory managers and supervisors
Production managers and supervisors
IT/IS managers and system administrators
Venue: Hilton Zurich Airport, Switzerland
Venue Phone: (888) 717-2436
Venue Type: Indoor - Hotel
Show Owner:ComplianceOnline

Booth Size Booth Cost   Available Amenities
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  Water: n/a
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  Marketing Vehicles Allowed: Call
Other Booth Sizes Available: n/a

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