chevron_left Categories

Other related webinars

US FDA Regulations: Food, Drugs, Biologics and M...

Friday, 9th December, 2011
Time : 02:00 PM | 11:00 AM

FDA GLP compliance in conducting non-clinical re...

Friday, 13th January, 2012
Time : 02:00 PM EST | 11:00 AM PST

FDA BIMO Inspection: Do's and Don'ts

Friday, 24th February, 2012
Time : 02:00 PM EST | 11:00 AM PST

FDA Compliant Practice for Labeling and Off-Labe...

Friday, 30th March, 2012
Time : 02:00 PM EST | 11:00 AM PST

FDA Compliant Good Laboratory Practice (GLP) For...

Friday, 11th May, 2012
Time : 02:00 PM EST | 11:00 AM PST

Conducting Successful FDA Meetings

Friday, 19th April, 2013
Time : 01:00 PM EST | 10:00 AM PST

Best Practices for Preparation for, Behavior dur...

Friday, 5th December, 2014
Time : 01:00 PM EST | 10:00 AM PST

Understanding the Mindset of an FDA Employee

Thursday, 2nd April, 2015
Time : 11:30 AM EDT | 04:30 PM CET

FDA's Import Requirements and Managing the Impor...

Friday, 24th April, 2015
Time : 11:30 AM EDT | 04:30 PM CET

UDI and GUDID - The Unique Device Identification...

Friday, 8th May, 2015
Time : 01:00 PM EST | 10:00 AM PST

Good Distribution Practices

Friday, 26th June, 2015
Time : 02:00 PM EST | 11:00 AM PST

Premarket and Postmarket Data Collection - A Fas...

Friday, 28th August, 2015
Time : 01:00 PM EDT | 10:00 AM PDT

FDA’s ‘Refuse to Accept’ Process for 510(k...

Friday, 30th October, 2015
Time : 02:00 PM EDT | 11:00 AM PDT

FDA Medical Device Regulation – Effective Cor...

Wednesday, 9th December, 2015
Time : 02:00 PM EDT | 11:00 AM PDT

Protecting Patient Privacy

Monday, 25th April, 2016
Time : 01:00 PM EDT | 10:00 AM PDT

Best Practices for FDA Inspection: Preparation, ...

Friday, 27th May, 2016
Time : 01:00 PM EST | 10:00 AM PST

Navigating FDA Import Requirements for Food, Dev...

Friday, 3rd March, 2017
Time : 01:00 PM EST | 10:00 AM PST

FDA Warning Letter, FDA-483's and Import Alerts ...

Friday, 13th October, 2017
Time : 01:00 PM EST | 10:30 AM PST

A Bulletproof, Cost-efficient Supplier Managemen...

Friday, 12th January, 2018
Time : 01:00 PM EDT | 10:00 AM PDT

FDA Good Clinical Practice (GCP) for Drugs, Biol...

Friday, 8th June, 2018
Time : 01:00 PM EST | 10:00 AM PST

FDA Case Scenarios – Best Practices for Managi...

Friday, 14th December, 2018
Time : 01:00 PM EDT | 10:00 AM PDT

Registries - The latest FDA trends, Reducing Cos...

Friday, 26th June, 2020
Time : 01:00 PM EST | 10:00 AM PST

CAPA and Critical Documentation of Clinical Tria...

Friday, 7th May, 2021
Time : 01:00 PM EST | 10:00 AM PST

Fellowship in Clinical Cardiology

Thursday, 4th November, 2021
Time : 01:00 PM EST | 10:00 AM PST

Fellowship in 2D Echocardiography – Edition II...

Friday, 7th January, 2022
Time : 01:00 PM EST | 10:00 AM PST

FDA and Medical Device Advertising in the 21st C...

Friday, 20th January, 2023
Time : 01:00 PM EST | 10:00 AM PST

Capturing Justifications in Change Control, Risk...

Friday, 27th January, 2023
Time : 01:00 PM EST | 10:00 AM PST

FDA Good Clinical Practice and More! HOW TO PLAN...

Friday, 10th February, 2023
Time : 01:00 PM EST | 10:00 AM PST

How FDA Trains Its Investigators to Review CAPA,...

Friday, 31st March, 2023
Time : 01:00 PM EST | 10:00 AM PST

How FDA Evaluates Your Quality Management System...

Thursday, 22nd February, 2024
Time : 01:00 PM EST | 10:00 AM PST

Recorded Webinar

A Bulletproof, Cost-efficient Supplier Management Program

timelapse 60 mins with 10-15 mins of Q and A

Note:

This webinar occured in the past
Along with recorded webinar, copy of presentation slides will be shared
Recorded Webinar can be played unlimited times

Speaker/Presenter

Short Abstract

A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA cannot regulate component suppliers, it is imperative that your company's purchasing and supplier control requirements provide the assurance that only acceptable components are used to manufacture finished devices. Most medical device manufacturers have acceptable systems in place to assure component quality. But what about supplier quality? Your company must have a procedure in place that describes the methods you use to evaluate potential suppliers, and set forth requirements that your suppliers must meet to be considered “approved.” You must also have a system in place to routinely assess your suppliers, and set forth the applicable criteria they must meet to remain “approved.” You may never have to pay a visit to your supplier if you have a great supplier control program in place.

The presentation will cover the following areas:

  • QSR and ISO 13485 requirements for supplier selection and assessment
  • How to qualify new suppliers in a cost efficient manner
  • How to assess current suppliers in a cost efficient manner
  • How to perform supplier-related corrective action
  • Minimum documentation requirements for supplier qualification, assessment, and related corective action


Apply for this webinar

Content Disclaimer

Contents in our website are from external websites. Links to and content from external website are provided for the convenience of users. Biopractice.com takes no responsibility for the content of such links and websites.

//