Achieving excellence in Mass production |Product Development and Implementation

Achieving excellence in Mass production |Product Development and Implementation

Outsourcing mass production overseas carries the challenge of ensuring the consistency and quality of each product – especially when multiplied by large volumes. Quasar’s high quality manufacturing standards are supported by robust processes at every stage of the process. Each process is broken down into several micro-actions that can be controlled accurately. This method ensures better control of each process as well as consistency.

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oem audit

How to Conduct an OEM Audit for a Medical Contract Manufacturer

Conducting a medical device manufacturer audit, includes a multitude of items to examine. Especially when considering the gamut of OEM activities: from simpler manufacturing operations, to vertical production facilities. In this article we cover the most important items to consider, as well as some additional factors that demonstrate above average OEM operations.

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EU MDR 2020: What to Expect

The EU MDR allowed a 3-year transition period for medical device manufacturers to comply. This runway ends in May 2020, where after the EU MDR comes into full effect. After this point, every part of the medical device supply chain from manufacturers to importers and distributors in the EU, will be required to comply.

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