Technipaq's Crystal Lake, Illinois production facility has received ISO 9001 certification of compliance with the International Organization for Standardization for quality management and quality assurance and ISO 13485 medical device certification.
Technipaq is a manufacturer of flexible sterilizable packaging materials for the medical device, diagnostic, healthcare, food and pharmaceutical industries.
Technipaq’s 60,000 square foot manufacturing facility, with 120 employees, provides laminating, flexographic printing, slitting, sheeting, die-cutting and fabricating of flexible bags and pouches for the healthcare industry.
In addition, Technipaq produces both custom and stock laminates in-house.
ISO 9001 is a 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.