Technipaq Achieves ISO 9001 and ISO 13485 Certifications
Technipaq Inc., a manufacturer of flexible sterilizable packaging materials for the medical device, diagnostic, pharmaceutical, and other industries, announces its 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 its Crystal Lake, IL, facility.
“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,” said Phil Rosenburg, president/CEO of Technipaq Inc., in a press release. "ISO 13485 is especially important as it makes us compliant with the same standards as our medical device manufacturing customers. 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.
Technipaq’s 60,000-sq-ft manufacturing facility, with 120 employees, handles laminating, flexographic printing, slitting, sheeting, die-cutting, and fabricating of flexible bags and pouches. In addition, Technipaq produces both custom and stock laminates in-house.
For further information, visit www.technipaq.com