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Event :FDA-Regulated Environment Development Team - 2017

Date :Thursday July 13th, 2017

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


 

Further information

Overview:  
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: support@compliance4All.com

Full Details & Registration Link:

http://www.compliance4all.com/control/w_product/~product_id=501361LIVE?channel=doctorama_Jul_2017_SEO

Further information

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Announcer

Compliance4All
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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Details

FDA-Regulated Environment Development Team - 2017 Pharmacy - Medicine - Bio-Technologies - Computer science - Management - Public Health
business analysts, software, medical device webinars, 21 cfr part 11 compliance, clinical diagnostics, medical device engineering, medical imaging, medical-device fabrics manufacturing
Professionals, Business Analysts Requirements Analysts Product Managers Portfolio Managers
100 1 --
English

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