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Vendor Qualification - How to Design and Implement an Efficient and Compliant Vendor Program
- Identifying the necessary quality functions of your facility
- Evaluating the capabilities of your facility in terms of quality services
- Putting together a request for proposals
- Evaluating vendors both on service and price
- Understanding when and how to compliment vendor services in-house
- How to integrate vendor information into internal systems
Overview of the webinar
It’s not realistic for a facility to be able to meet all of its quality needs in-house without incurring an inordinate expense. That said, it may become expensive to outsource everything, and it may waste resources to outsource certain quality activities. The goal of this webinar is to make sure that any outsourcing decision is well thought-out.
Who should attend?
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
Why should you attend?
In this session, you will learn how to understand your quality needs, understand what can be outsourced and set up a plan. You will learn how to properly evaluate vendors, understand their capabilities as compared to your facilities needs and pick the best vendors based on service and price. This webinar will also teach you how to properly monitor an outsourcing program, determine areas of concern and allow you to evolve the program as needed. This webinar will teach you when to implement complimentary activities to an outsourced quality function and how to integrate this information into a fully-functioning program.
Faculty - Mr.Todd Graham
Todd Graham, is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. Mr. Graham 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.