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How Online Videos Have Optimized Researching Manufacturing Equipment
Technology is developing at a rapid rate in the Life Science and Medical Industries. Processes that were once carried out by hand, or developed with slow and tedious...
Thoughts From a Material Sourcing Millennial
It’s Monday morning and I have 5 material sourcing projects laying on my desk that I need to work through before my 10 AM sales call where I need to deliver updates to...
5 Tests Critical to the End Use Applications of Nonwovens
Nonwovens testing of physical and mechanical properties are essential to determining their end-use applications. For example, if a nonwoven has high absorptive capacity,...
How to Improve Manufacturing Workflow: 5S and Gemba Walks
Every medical production facility strives to provide a safe and efficient work environment for its operators to succeed. When it comes to process improvement, the focus...
5 Essential Activities of Current Good Manufacturing Practices
Medical Device manufacturing has to comply with FDA guidelines and regulations for tracking each and every step of the manufacturing process, including raw material...
3 Keys to Strong Supply Chain Management
Supply chain management plays a key role in the success of any business. Building a strong relationship with your suppliers within your supply chain will allow you to...
Continual Improvement Driven by Quality
If you are familiar with medical device manufacturing, certainly you have heard the phrase, “Quality over Quantity.” This phrase is commonly used to denote that it is...
Identifying & Understanding the 8 Wastes
When considering potential waste in a medical manufacturing facility, most precision manufacturer’s first thoughts are only on the material waste. In fact, there are 8...
Effective Guidelines to Launch a Medical Device Product
Developing and commercializing a new product is an exciting and dynamic process. Unfortunately, more products fail to launch than actually do launch and many times this...
The FDA Regulatory Pathway for Premarket Notification 510(k)
The FDA regulatory pathway for Premarket Notification 510(k) is required by anyone who intends to market a Class I, II, or III device in the United States intended for...