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Webinar on “Building a Vendor Qualification Program for FDA Regulated Industries” from GlobalComplia

Education

(Free Press Release) GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a webinar on the topic, “Building a Vendor Qualification Program for FDA Regulated Industries” on June 12. Jonathan M. Lewis, a senior regulatory affairs and compliance professional, will be the Speaker at this session.

Webinar on “Building a Vendor Qualification Program for FDA Regulated Industries” from GlobalComplia


      

Description:

Being conscious of the products and services purchased is not only good practice for consumers and most businesses; it is a regulatory requirement for FDA-regulated industries. Decisions relating to where to purchase components, raw materials, manufacturing and testing equipment, and even consulting services, need to be well informed, as well as documented, for FDA-regulated industries.

Ill-informed purchasing decisions can lead to situations that impact product quality, regulatory compliance, company profits, and even the reputation of the company. This webinar offers a practical and compliant methodology for firms in FDA-regulated industries to qualify vendors and hence make well informed purchasing related decisions.

Building a sound vendor qualification program is necessary for organizations that consistently waste time on finding qualifying vendors that cannot or will not meet their requirements. It is for those organizations whose approach to vendor qualification and vendor audits leave them with internal CAPAs, customer audit items, or 483 observations, and for those who wonder if an onsite vendor audit is necessary in the eyes of FDA.

This webinar answers important questions pertaining to a vendor qualification program. The speaker will:

o Define a sustainable structure for a vendor qualification program

o Explain how change control and other quality programs feed into the vendor qualification program

o Discuss compliant, yet sustainable, SOP, forms, and templates associated with vendor qualification

o Explain how to determine the best potential vendor and what a potential vendor needs to supply before qualification

o Explain how to initially identify vendors that meet your requirements prior to qualification

o Explain how to perform on-site and off-site verifications

o Explain how to monitor and re-qualify vendors

o Explain how to estimate costs and time associated with vendor qualification

o Explain how to respond to customer and regulatory audit observations associated with vendor qualification

o Discuss common pitfalls to avoid when qualifying vendors

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When: June 12, 10:00 AM PDT | 01:00 PM EDT

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By whom:

Jonathan M Lewis has about two decades’ experience in the areas of quality control/quality assurance (QA/QC), regulatory affairs, validation, and project management in both industry and consulting roles

 

Mr. Lewis has experience in the medical device, diagnostic, biopharmaceutical, pharmaceutical, cosmetic, nutritional supplement, food, and animal food industries

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For whom:

The webinar will benefit

o Internal Auditors

o Regulators

o Legal Departments

o Compliance Officers

o Purchasing Managers

o QC Managers

o QA Managers

o Quality and Sales Department Staff

o Compliance Consultants

o Senior Management

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Duration: 60 minutes

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To enroll for this webinar, contact

This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Ph: 800-447-9407

 

Fax: 302-288-6884




Webinar on “Building a Vendor Qualification Program for FDA Regulated Industries” from GlobalComplia

Source: Press Release

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