Hazard Analysis following ISO 14971

7 years ago Posted By : User Ref No: WURUR12164 0
  • Image
  • TypeWebinar
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  • Location New York, United States
  • Price
  • Date 07-06-2017
Hazard Analysis following ISO 14971, New York, United States
Webinar Title
Hazard Analysis following ISO 14971
Event Type
Webinar
Webinar Date
07-06-2017
Last Date for Applying
07-06-2017
Location
New York, United States
Organization Name / Organize By
Compliance Global Inc.
Organizing/Related Departments
Compliance Global Inc.
Organization Type
OTHERS
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Business Development

Biotechnology

Location
New York, United States

Overview

The US FDA expects that as part of a product development Design Control Program risk management will be conducted.

FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard.

One of the techniques described in ISO 14971 is Hazard Analysis. This is the most powerful of the risk management techniques because it considers risks in normal operation as well as fault conditions. FMEA and FTA consider only fault conditions and are more suited as reliability tools than as product safety tools.

In this ISO 14971 risk management training we will explain in detail the process of conducting a hazard analysis. The confusing terms “hazard”, hazardous situation”, “harm”, “causative event”, “ALARP”, “risk index”, “residual risk” will be explained. We will go step by step through a template for hazard analysis so that the process is clear. Examples of hazards and hazardous situations will be discussed. Also, how to deal with residual risk will be discussed. We will go step by step through a typical hazard analysis.

We will explain how to integrate Human Factors studies into the Hazard Analysis and how to integrate Hazard Analysis into the design program.

Why Should You Attend

FDA expects that as part of a product development program risk management will be conducted. FDA recommends using ISO 14971 as a guide and has accepted it as a recognized standard. Hazard Analysis is the most powerful of the risk management tools described in ISO 14971 but it is very confusing. Many new concepts are introduced. we will explain these concepts and provide examples so that the process is clear.

Areas Covered in this Webinar

explanation of Hazard Analysis terms hazard analysis process explanation using a template examples of terms will be given hazard analysis examples will be covered step by step

Learning Objectives

Learn to conduct a meaningful hazard analysis

Who Will Benefit

  • Engineering personnel
  • Software developers
  • QA
  • Management

For more detail please click on this below link: http://bit.ly/2moVzlU

Email: [email protected]

Toll Free: +1-844-746-4244

Tel: +1-516-900-5515

Fax: +1-516-900-5510

Others Details

In this webinar, our expert will explain in detail the process of conducting a hazard analysis. Book for this ISO 14971 risk management training now!

Registration Fees
Available
Registration Fees Details
Live Session for one participant Price: $199 Corporate Live Session Group - Max 10 Participants from one Location.(For multiple location please contact our customer support team) Price: $549 Recorded Session Get unlimited access to the link for six months. Login information will be shared 24 hours after the completion of Live webinar Price: $219 Training CD Free shipment within 72 Hours, from the date of webinar completion Price: $399
Registration Ways
Email
Phone
Website
Post Box
Other
Address/Venue
  Online Webinar 
Official Email ID
Contact
Compliance Global Inc.

2754 80th Avenue, New Hyde Park, NY 11040

[email protected]

   5169005515      5169005515
   Fax No: 5169005515
Compliance Global Inc.

2754 80th Avenue, New Hyde Park, NY 11040

[email protected]

   5169005515      5169005515
   Fax No: New York