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2015 International Symposium on Social Sciences and Management ISSSM 2015
2/3/2015 8:00 AM - 2/5/2015 5:00 PM
TOSHI CENTER HOTEL Tokyo Japan
Event Listing
Summary:

All theoretical, empirical and practical papers from scholars and professionals in the above fields are all highly welcome.

2015 Seoul International Conference on Life Sciences and Biological Engineering SICLSBE
1/8/2015 8:00 AM - 1/10/2015 5:00 PM
Courtyard Seoul Times Square Seoul South Korea
Event Listing
Summary:

The Seoul International Conference on Life Sciences and Biological Engineering (SICLSBE) will be held in Seoul, Korea from January 8 to 10, 2015.

2015 Seoul International Conference on Social Sciences and Management
1/8/2015 8:00 AM - 1/10/2015 5:00 PM
Courtyard Seoul Times Square Seoul South Korea
Event Listing
Summary:

2015 Seoul International Conference on Social Sciences and Management (SICSSAM) is scheduled to take place in Seoul, Korea, from January 08-10, 2015.

21 CFR Part 820 Quality System Regulation Applying Principles of Lean Documents
7/30/2014 10:00 AM - 11:00 AM
Online Event Fremont, California United States
Event Listing
Summary:

All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records. Medical device manufacturing plants, required to follow 21 CFR Part 820, have the additional responsibility to ensure that each and every step of the manufacturing process is controlled by work instructions, SOPs, set-up instructions, equipment maintenance, and support functions, and that evidence of this work is maintained by controlled records.

2day Inperson Seminar on Advanced Course Validation and 21 CFR 11 Compliance of Computer Systems
7/24/2014 9:00 AM - 7/25/2014 6:00 PM
WILL BE ANNOUNCED SOON San Francisco, California United States
Event Listing
Summary:

This course will build on the Validation and 21 CFR 11 Compliance Basic Course, to give hands on experience on executing on the computer systems validation of a system, and to discuss related activities such as Validation Master Plan, Infrastructure Qualification, Project Management for Validation and Validation of Test Tools

2day Inperson Seminar on Applied Statistics for QA QC Manufacturing and Design Control
7/24/2014 9:00 AM - 7/25/2014 6:00 PM
WILL BE ANNOUNCED SOON San Francisco, California United States
Event Listing
Summary:

This seminar provides a practical approach to understanding how to interpret and use a standard tool-box of statistical methods, including confidence intervals, t-tests, Normal K-tables, Normality tests, confidence/reliability calculations, AQL sampling plans, measurement equipment analysis, and Statistical Process Control.

2day Inperson Seminar on Global Medical Device Regulation at Denver CO
7/31/2014 9:00 AM - 8/1/2014 6:00 PM
WILL BE ANNOUNCED SOON
Event Listing
Summary:

This course provides an overview of international medical device regulations. Beginning with a discussion of the similarity of global requirements, including both voluntary and mandatory standards and directives, and progressing to in-depth analyses of market specific requirements, the course provides the student with resources to meet the regulatory requirements for the largest world markets.

2day Inperson seminar on Mastering the HIPAA Privacy Security and Breach Notification Rules
7/17/2014 9:00 AM - 7/25/2014 6:00 PM
WILL BE ANNOUNCED SOON
Event Listing
Summary:

The session provides the background and details for any manager of healthcare information privacy and security to know what are the most important privacy and security issues, what needs to be done for HIPAA compliance, and what can happen when compliance is not adequate.

3rd International Conference on Civil Engineering and Engineering
2/3/2015 8:00 AM - 2/5/2015 5:00 PM
TOSHI CENTER HOTEL Tokyo Japan
Event Listing
Summary:

This conference provides opportunities for the delegates to exchange new ideas and application experiences face to face, to establish business or research relations and to find global partners for future collaboration.

A Comprehensive View of FDA Regulations for Medical Devices 2 Day InPerson Seminar
7/22/2014 8:30 AM - 7/23/2014 4:00 PM
Courtyard Chicago Downtown/River North chicago, Illinois United States
Event Listing
Summary:

Don’t let a common misunderstanding get you into trouble! There is more to the US Medical Device Regulations than Part 820.

Companies that don’t understand will face regulatory scrutiny and receive FDA Form 483s and Warning Letters. Recently a device manufacturer got a Warning Letter relating to updates to shipped devices, which said, “The Quality Manager stated he was unaware of the corrections and removal reporting and recordkeeping requirements.”

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