FDA Compliant Vendor Validation Programs
Date: February 14, 2025
Duration: 60 Minutes
Time: 12 PM EST
In this webinar, we would discuss various aspects of vendor operations, common issues often overlooked, simplified solutions and oversight of vendors by sponsors. Lifecycle management and dynamic contracts will be discussed. This webinar will help attendees learn the best ways to create an ongoing vendor qualification and validation program. It will discuss common issues to avoid when it comes to vendor selection and management.
In an FDA-regulated industry, sponsor companies are only as compliant as their vendors. Any violations at the vendor are liabilities for the sponsoring company. The sponsor is held responsible for its poor vendor selection, vendor non-compliance, and lack of vendor oversight. Sponsors using bad vendors suffer the financial, regulatory, and legal consequences. Similarly for the vendors it is equally critical to have transparent relations with the client.
You need to attend this webinar, if:
- You have wasted time on qualifying vendors that you know cannot or will not meet your requirements.
- Your approach to vendor qualification and vendor audits has led to internal CAPAs, customer audit items, or 483 observations.
- You are unsure whether an onsite vendor audit is necessary as per the FDA
This webinar is designed to help the companies of any FDA regulated products to build or develop a sustainable vendor qualification program.
- FDA requirements for your Vendor
- Aspects of Vendor Qualification
- Vendor Qualifications checklist and forms
- Best Practices for Vendor-Client Relationship
- Vendor Audits
- How to change Vendors
- Quality Agreements
This course will provide valuable assistance and guidance to all FDA regulated companies for building sustainable vendor qualification program. The following job titles/ positions will benefit from attending this seminar:
- QA professionals
- Contracting professionals
- Regulatory specialists
- Legal Departments
- Compliance Officers
- Purchasing Managers
- QC Managers
- QA Managers
- Quality and Sales Department Staff
- Compliance Consultants
- Senior Management
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
We accept credit card, debit card, and PayPal.
Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
