iBase-t Experts

In the world of medical device manufacturing, mistakes on the plant floor can have dire consequences. That’s why meeting FDA requirements such as 21 CFR Part 820, 21 CFR Part 11 and ISO 13485 are so critical.

The bi-annual EURONAVAL event is said to be the world’s largest meeting of naval technologies with 355 exhibitors, over 400 journalists and nearly 25,000 trade visitors.

iBase-t conducted a survey among Manufacturing Technology experts to identify topics of the utmost importance to those working within the manufacturing industry.

Tackling the price of quality goes beyond reducing the number of defects. It involves evaluating the entire quality management system.

Conrad Leiva, Vice President of Product Strategy and Alliance will be presenting as part of two different speaking sessions at Deltek Insight 2016.

In today’s global medical device manufacturing environment, supply and manufacture is more dispersed and nuanced than it ever has been.

Starting a new project, a new initiative, or new journey to a new product solution causes a variety of questions to arise when trying to find a Manufacturing Execution System (MES)

The Solumina MES can quickly identify your defect, stop production anywhere in operations, then diagnose and resolve the problem so production can resume.

On September 1, 2016 iBase-t celebrated the opening of their new office space and improved working environment in India.