Accessibility, Advantages and Challenges of 3D Printing for Designers and Developers

In an article that addresses the accessibility of 3D printing to today’s businesses as well as hobbyists and designers, Nermin Hajdarbegovic, technical editor for toptal, helps to clarify the difference technologies as well as the benefits and challenges of taking on 3D printing. Hajdarbegovic states, “3D printing is not a new technology, but recent advances in several fields have made it more accessible to hobbyists and businesses.” He also poses some important questions.

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Topics: medical manufacturing, 3D Printing

Join KMC at Molecular Med TriCon 2017 in San Francisco

In just a few short days, over 3,500 life sciences professionals will be gathering at Molecular Med Tri-Con 2017 in San Francisco, February 19-24. Discover the latest developments in molecular medicine, genomics, diagnostics and information technology. KMC Systems will be at booth 123. Here's what you can expect to see at this year's #TRICON

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Topics: Trade Shows, Molecular Med Tri-Conference

Explore Life Sciences with KMC at SLAS2017!

What to expect at SLAS 2017

The KMC Systems team is headed to Wasthington DC for SLAS 2017, February 4-8! Industry leaders in life sciences, diagnostics and emerging technologies will meet at the Walter E. Washington Convention Center for SLAS 2017. Be sure to visit KMC at booth #1601! Here's what to expect at this year's SLAS conference. 

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Topics: SLAS

Important Changes to ISO 13485 2016 for Medical Device Manufacturers, Designers

In 2016 new ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes were published. This set into play a new international framework for requirements in an effort to mitigate risk in the production of compliant, reliable medical devices. Companies are granted a 3-year transition period. Are you ready? 

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Topics: quality assurance, regulatory control, ISO 13485

Free SLAS2017 Exhibit Pass or $100 Off Full Registration*

If you haven't already signed up for your SLAS2017 exhibit pass or full conference pass, now is the time. KMC Systems and SLAS are offering a free exhibit pass or $100 off full conference registration for first time attendees*.

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Topics: SLAS2017

The Benefits of Co-located Engineering and Manufacturing Teams

Need engineering and manufacturing expertise to bring your product from concept through production? It helps to chose a firm that offers both engineering and manufacturing as part of a total product lifecycle approach. Keeping your project under one roof optimizes invention and mitigates risk during the transition from engineering and design to production. Medical Device Developments spoke with KMC's Mike Kallelis about this very topic.

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Topics: medical contract manufacturing, Total Product Life Cycle, medical engineering

Expansive Growth Predictions; Medical Device Manufacturing 2017



The medical device market is growing at a rapid rate. With advancements in technology and manufacturing capabilities, medical instrument companies are seeking accelerated time to market and improved quality and cost control. How do these changes influence market sales and the selection of an outsourcing partner?  

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Topics: medical device manufacturing, 3D Printing

Today's the Last Day for AMP 2016 Advanced Registration! Register now.

In less than 3 weeks industry leaders in molecular medicine will gather for the Association for Molecular Pathology (AMP) 2016 Annual Meeting in Charlotte, North Carolina. Today is the last day for advanced registration! If you haven't registered yet, you can do so right here: 

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Topics: Trade Shows, molecular medicine

4 Types of FDA Inspections and What They Mean to Medical Manufacturers

There are many different criteria which medical manufacturing companies and medical instrument companies are required to meet for FDA approval. One of these areas is the inspection of medical device manufacturers.  If you are in the medical instrumentation industry, how do you successfully and seamlessly bring compliant medical devices to market? 

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Topics: KMC Systems, Medical Product Manufacturing, medical device manufacturing, medical device design and manufacturing, medical device quality assurance

Strategies and Standards for Medical Device Signal Detection

In 2012, the Center for Devices and Radiological Health (CDRH), a branch of the U.S. Food and Drug Administration, announced four long term strategies to strengthen its National System for Medical Device Post-Market Surveillance1. Find out how these strategies correlate with medical device signal detection and why medical device firms can benefit from selecting a contracting partner with experience in Pharmacovigilance requirements.

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Topics: quality assurance, regulatory control