Other related webinars
Are Genes Patentable in the United States? (A Re...
Friday, 26th August, 2011
Time : 02:00 PM | 11:00 AM
GLP Regulations – A Simplified Overview for Ac...
Friday, 2nd December, 2011
Time : 02:00 PM | 11:00 AM
Understanding FDA Guidance on GLP for Nonclinica...
Thursday, 22nd December, 2011
Time : 02:00 PM EST | 11:00 AM PST
FDA and EMA successful development and approvals...
Friday, 22nd June, 2012
Time : 02:00 PM EST | 11:00 AM PST
Strategic insights into European (CHMP/EMA) and ...
Monday, 3rd December, 2012
Time : 02:00 PM EST | 11:00 AM PST
FDA Approvals and Insights: Understanding US-FDA...
Friday, 1st March, 2013
Time : 02:00 PM IST | 09:30 AM CET
Effective Responses to FDA Warning Letters on Qu...
Friday, 15th August, 2014
Time : 01:00 PM | 10:00 AM
FDA’s view of Purchasing Controls, regulatory ...
Friday, 3rd October, 2014
Time : 01:00 PM EST | 10:00 AM PST
A review of the FDA’s oversight, regulatory re...
Friday, 16th January, 2015
Time : 01:00 PM EST | 10:00 AM PST
Preparing for and Managing EU Notified Bodies Au...
Thursday, 28th January, 2016
Time : 01:00 PM EDT | 10:00 AM PDT
Biopharmaceutical Method Transfer – Using a Qu...
Friday, 20th May, 2016
Time : 01:00 PM EDT | 10:00 AM PDT
Quality systems for Analytical Instrumentation a...
Friday, 24th June, 2016
Time : 01:00 PM EDT | 10:00 AM PDT
Effective Investigation of Deviations & Putting ...
Friday, 2nd September, 2016
Time : 04:00 PM IST | 11:30 AM BST
NO More Written Procedure (Standard Operating Pr...
Friday, 14th October, 2016
Time : 01:00 PM EDT | 10:00 AM PDT
Best Practices in Supplier Management: Evaluatio...
Friday, 20th January, 2017
Time : 10:00 AM EST | 04:00 PM BST
Using Quality Indicators for Successful FDA QSR ...
Friday, 10th February, 2017
Time : 04:00 PM IST | 11:30 AM BST
Effective Management Reviews for FDA and Managem...
Friday, 21st April, 2017
Time : 01:00 PM EDT | 10:00 AM PDT
FDA Internal Audits - An Important Tool for Avoi...
Friday, 30th June, 2017
Time : 04:00 PM IST | 11:30 AM BST
FDA Regulatory Rules for Supply Chain and Manufa...
Friday, 4th August, 2017
Time : 11:00 AM EDT | 08:00 AM PDT
FDA - Training Modules
Friday, 28th September, 2018
Time : Set the Time | Set the Time
FDA Quality Systems Inspection Technique (QSIT) ...
Friday, 26th October, 2018
Time : 01:00 PM EDT | 10:00 AM PST
Key Element of Quality Management System Complia...
Friday, 30th August, 2019
Time : 04:00 PM IST | 11:30 AM BST
A CAPA Primer - Elements of a CAPA Program
Friday, 28th February, 2020
Time : 01:00 PM EST | 10:00 AM PST
How To Respond To FDA 483s
Wednesday, 2nd March, 2022
Time : 01:00 PM EST | 10:00 AM PST
FDA Expectations from Supplier Management for GM...
Friday, 22nd April, 2022
Time : 01:00 PM EDT | 10:00 AM PDT
The clinical, regulatory and business challenges...
Friday, 19th August, 2022
Time : 01:00 PM EST | 10:30 AM PST
The FDA CGMP and Data Integrity in Pharmaceutica...
Friday, 7th April, 2023
Time : 01:00 PM EST | 10:30 AM PST
FDA PMA Submissions - Contents, Process, Pitfall...
Friday, 21st April, 2023
Time : 01:00 PM IST | 10:00 AM PST
Complaint Handling in Compliance with FDA and IS...
Friday, 26th May, 2023
Time : 01:00 PM EST | 10:00 AM PST
Recorded Webinar
FDA Expectations from Supplier Management for GMP
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
To attend this webinar kindly call 1-646-216-8860 or email at marketing@biopractice.com
This training program will provide participants with a working knowledge of supplier audits. The why, when, who, how, and what of conducting a supplier audit will be reviewed to ensure that your supplier can meet all your expectations. When contemplating the use of a supplier you would normally have many requirements and expectations that must be met. These include technical, regulatory, quality, responsiveness, location, readiness, and those less defined but critical. One of the tools at your disposal to verify the supplier’s acceptability is to audit the operation.
Why should you attend
Many organizations conduct supplier audits because they are required to do so by their customers or a regulatory agency. Others conduct the audits because they have been led to believe that it's a good tool for comparing various suppliers against an arbitrary list of criteria.
The presentation will cover the following areas:
- Why audit your supplier?
- Who will audit your supplier?
- When will you audit your supplier?
- What will you audit?
- How will you conduct the audit?
- How to prepare a pre-audit questionnaire
- Areas to be audited and using check lists
- How to conduct effective close out meetings
- The advantages and disadvantages of using numerical audit scores
- Issuing observation reports and recommendations to your management and to your potential suppliers
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.