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Understanding and Implementing the Medical Device Directive 2Day Inperson Seminar
7/25/2014 8:30 AM - 4:00 PM
Courtyard Chicago Downtown/River North chicago, Arizona United States
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Summary:

This course will address the details of the MDD and includes other significant issues such as the Quality Management System (EN ISO 13485:2012), Risk Management (EN ISO 14971:2012), Clinical Evaluation (MDD Annex X), the role of harmonized standards, and the vigilance system.

Coding and Cupcakes
7/26/2014 9:00 AM - 12:00 PM
Sprint Accelerator Kansas City, Missouri United States
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Summary:

Join us for a brand new coding series, Coding & Cupcakes. Mothers and daughters are invited to attend sessions to learn about code and how to build websites together.

Best Practices in Supplier Management
7/29/2014 10:00 AM - 11:00 AM
Online Event Fremont, California United States
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Summary:

Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.

FDA Device Software Regulation
7/29/2014 10:00 AM - 11:00 AM
Online Event Fremont, California United States
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Summary:

Software's level of complexity and use is expanding at exponential levels. Likewise the potential risks to health follow suit. Problems with software create a number of different hurdles. Software may be a standalone device, control a device's performance, make calculations, identify treatment options or begin to play a more active role in making clinical decisions regarding patient management and treatment.

Whats New in Windows Server 2012
7/29/2014 10:00 AM - 11:30 AM
Online seminar Fremont, California United States
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Summary:

Why should you attend: What do you get when 10,000 engineers work on developing a software product for four years? Windows Server 2012, of course. There are literally hundreds of new features in this exciting version of server operating system. Before you deploy Windows Server 2012 in your environment, take a closer look at the new features presented in this Webinar.

Areas Covered in the Session:

The New Windows Server 2012 Interfaces

Navigating the Server

Sign Out, Shutdown, & Restart

Server Manager Dashboard

Windows Server 2012 Storage Spaces

What are Server Groups?

The New File Explorer

What's New in Virtualization?

What's New in the File System?

What's New in RDP?

What's New in SMB Support?

What's New in Active Directory?

What's New in DNS?

What's New in BitLocker?

What's New in Smart Cards?

What's New in Security Auditing?

What's New in File Storage?

What's New in Task Manager?

Speaker Profile:

Zubair Alexander is a Microsoft MVP, a Microsoft Certified Trainer, and the founder of SeattlePro Enterprises, LLC, an IT training and consulting company. He holds more than 25 industry certifications including MCT, MCSE, MCSA, MCDST, MCITP, MCTS, MCP+I, MCSA 2000/2003: Security, MCSE 2000/2003: Security, CNA, A+, Network+, Security+, CTT+ and CIW. His experience covers a wide range of spectrum: trainer, consultant, systems administrator, security architect, network engineer, author, technical editor, college instructor and public speaker.

DevOps Kansas City Michael Goetz of Chef
7/29/2014 5:30 PM - 8:30 PM
Red Nova Labs
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Summary:

Michael is a Sr. Consulting Engineer with Chef, where he helps customers manage their infrastructure automation.

Hack Night
7/29/2014 6:00 PM - 10:00 PM
Assembly Coworking Space Calgary Canada
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Summary:

Every Tuesday night from 6pm to 10pm, “Hack Nights” come alive with hustlers, hackers and hipsters coming together to work on their start-up ideas. If you are working on something tech related, and are in the pre-investment stage, this event is for you!

Weekly Open Make Night
7/29/2014 6:00 PM - 9:00 PM
Tampa Hackerspace Tampa, Florida United States
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Summary:

Lets get together to build some cool projects and meet some very cool people. Join us to work on your stuff, bounce ideas off of members and socialize.

Occasionally, we'll throw in a small class.

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
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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.

Combination Products FDAs Proposed Rule for GMP Requirements and Introduction and Expectations for
7/30/2014 10:00 AM - 11:00 AM
Online Event Fremont, California United States
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Summary:

What is a combination product? What are some examples of combination products? How are combination products assigned for review? Where can I find guidance for how master files can be used in the submission of information relevant to my combination product? Determine which Center will review my combination or non-combination product?

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