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Here's your one-stop resource for the medical device industry's most frequently asked questions—and answers! The Oliver Answer Team is continually updating our FAQ&A resource; check back often for the latest information on industry trends and regulations. Have a specific question? Ask the Oliver Answer Team.
 

FAQ: I'm getting ready to make a material conversion on one of my packaging lines. What can I do to maximize my chances for success and also minimize the timeline and amount of testing required for the project?

FAQ: My management is challenging me to reduce the cost of packaging. How can I lower my packaging material costs?

FAQ: What should be considered when designing a thermo form/fill/seal tool for a sterile medical package?

FAQ: How can I lower my packaging costs without fear of compromising quality?

FAQ: What kind of quality systems are medical device packaging suppliers typically required to employ?

FAQ: Are medical device packaging suppliers required to have electronic documentation systems that are compliant with FDA 21 CFR Part 11 (Electronic Records; Electronic Signatures) requirements?

FAQ: How can I determine the best top web material solution for a form/fill/seal device package application?

FAQ: When evaluating package seal strength, is there a correlation between peel strength and burst strength?

FAQ: Where can I find more detailed information regarding the physical properties (thickness variation, porosity, etc.) of Tyvek® and other materials?

FAQ: Are there any industry standards for creating specifications and tolerances for medical-grade pouches?
 

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