Vendor Qualification - How to Design and Implement an Efficient and Compliant Vendor Program

Instructor: Todd Graham
Product ID: 703066
Training Level: Intermediate
  • Duration: 60 Min
This webinar will tell you what you need to know to design a compliant vendor program, implement it throughout the organization, manage the necessary documentation and effectively communicate with vendors your requirements, needs and issues.

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Aug-2013

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

Why Should You Attend:

No one company can reasonably provide for all its possible needs for GLP/GMP compliant supplies. There is also a need to be able to reasonably adjust suppliers due to company needs, supplier issues, budgetary concerns and a whole host of other issues. In order to be able to manage your vendors properly, you need to figure out not only what materials you need from your vendors, but how you need them delivered, what information you need for regulatory reasons and how to manage relationships with your vendors as both your and their abilities change. In this seminar, you will learn how to develop, maintain and implement those relationships with vendors.

In addition, you will learn how to communicate with internal stakeholders about these relationships so you can effectively communicate your organization’s needs and help your internal stakeholders deal with the various issues they need to get work accomplished. No vendor program can work without internal buy-in from everyone in the organization, as it is rare that every need can be met by one set of vendors in a standard way. With this seminar, you will be able to learn the key factors needed in managing the needs of vendors.

After this seminar, you will be able to have an agile, efficient and compliant vendor program that will meet the needs of everyone in your organization while being cost-effective as needed. You will also be to deal with the vendors in a clear, defined manner which will allow them to provide the necessary materials you need in order to support company goals.

Areas Covered in the Webinar:

This webinar will help you learn how to develop and implement and effective vendor program. The webinar will include the following critical information you will need:

  1. What you need from your vendors and how to evaluate them
  2. What people within your company need
  3. How to learn the capabilities of your vendors
  4. How to manage the vendors based on their capabilities
  5. How to creative effective communication between internal stakeholders and your vendors
  6. How to manage a vendor program based on company needs

Who will Benefit:

This topic applies to personnel/ companies in the biotechnology and pharmaceutical industry. The employees who will benefit most include:

  • Senior management
  • Quality Assurance
  • Research and Development
  • Supply chain personnel
  • Project management
  • Process scientist
  • Regulatory Affairs
  • Audit

Instructor Profile:

Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertise are molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He is also in the process of establishing a consultancy that assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.

Follow us :
Latin America: Regulatory Compliance Requirements for Life Science Products
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

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