Technipaq Earns ISO 9001 and ISO 13485 Certifications

Technipaq Inc., one of the premier manufacturers of flexible sterilizable packaging materials for the medical device, diagnostic, healthcare , food and pharmaceutical industries, announces their ISO 9001 certification of compliance with the International Organization for Standardization for quality management and quality assurance and ISO 13485 medical device certification for production in their Crystal Lake, Illinois facility.

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“The certification achievement of ISO 9001 and ISO 13485 is a tribute to the tremendous commitment and dedication of our entire staff to consistently meet customer needs with the highest quality products. The ISO 13485 is especially important as it makes us compliant with the same standards as our medical device manufacturing customers,” said Phil Rosenburg, President/CEO of Technipaq Inc. “We are extremely pleased that our work has been recognized with this certification and are further committed to using only the best company policies and practices to deliver the premium products our customers expect and deserve.”

ISO 9001 is a comprehensive quality management and assurance certification, which represents the company's adherence to international standards on good management practices and policies that consistently meet customer quality requirements. ISO 13485 is a similar certification specifying international requirements on the ability to continuously provide medical devices and related services to meet regulatory and customer requirements.
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