Approved suppliers
Schedule:
- Available for private webinars
Duration: 2 hours with questions and answers
Synopsis: The process for identifying, evaluating, selecting and monitoring the firms who provide critical raw materials, components or services generates more questions then any other single ISO clause. How much effort is too much? Why won’t suppliers cooperate? This webinar will provide answers to these and many other questions as we describe what this process should look like including:
- What is a critical supplier?
- How do you evaluate a supplier who has a skill set you do not possess?
- Realistic monitoring process
- Letting poor performing suppliers go, and
- Creating appropriate objective evidence
Description: You need the right materials/services at the right time from suppliers you can trust and this webinar discusses how you can achieve that without burdening either yourself or your supply chain. We point out what is important and what is not and how to solicit cooperation from even the most disinterested suppliers. We will also describe a process that even the most diligent inspectors/auditors will like!
Who should attend: This webinar is ideal for regulatory/quality management staff, research and development teams, inventory or purchasing managers and executives of all types.
Presenter: Tim Duggins, Horizon Phoenix’s Senior Partner has more than 25 years experience in medical device quality systems and product testing. Tim is a skilled and fully accredited consultant and auditor with extensive experience implementing fully compliant regulatory and quality systems using EN/ISO 13485, USFDA QSR, Health Canada CMDR and/or all medical European Directives for more than 100 clients. An avidly sought after expert, he served as a consultant to such diverse organizations as federal governments, international non-governmental organizations, and industry from multi-national manufacturers to a three-person niche-market company. Tim has participated on numerous national and international committees writing product testing standards and helping create government regulatory processes; his product experience spans the entire medical device spectrum from high volume injection molded disposable products, digital radiography systems, in vitro diagnostic test kits to implantable cardiovascular devices.
Expert contributor: TBA
Registration:
$295
For more information or to pose a question about this webinar
contact: info@raqawebinars.com
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