FDA-Regulated Environment Development Team - 2017

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Category Business Analysts, Software, Medical Device Webinars, 21 CFR Part 11 compliance, clinical diagnostics, medical device engineering, medical imaging, medical-device fabrics manufacturing, contract lyophilization, clinical trial software

Deadline: July 12, 2017 | Date: July 13, 2017

Venue/Country: Online, U.S.A

Updated: 2017-05-16 20:27:24 (GMT+9)

Call For Papers - CFP

The Agile approach is well established in other industries adoption of Agile in medical device development has been increasing in the past five years.

Why Should you attend:

Medical device development struggles with huge pressures: the need for innovation, keeping cost down, and minimizing time to market. With all its success in other industries, it appears that the Agile approach be a huge should help - but even after years of use and multiple reports, criticism of, and doubts about, Agile methods exist in the medical device field.

Areas Covered in the Session:

Laying the Groundwork

Recognize your context

What Agile solves - and requires

Selecting a project to pilot

Change needs to be shepherded

Who Will Benefit:

Software Developers

Business Analysts

Requirements Analysts

Product Managers

Portfolio Managers

Speaker Profile:

Brian Shoemaker consults for healthcare products companies on computer system validation, software quality assurance, and electronic records and signatures. He has conducted validation both on product software and on internal software, developed software quality systems, audited software quality processes (including agile methodology), and evaluated 21 CFR Part 11 compliance.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com