The INVpack machines for the pharma sector comply GMP regulations and are designed and built under the strictest manufacturing standards. INVpack has specific suppliers for the materials that come in contact with the product, of which all documentation can be supplied. Among these documents, we can include certificates of materials, sealing, certificates 2.1 and 3.1, rugosity tests, riboflavin tests, X-rays and laparoscopy seal images.
As pharma documentation, INVpack can supply the DQ, IQ and OQ documentation, as well as the functional analysis of the machine or other type of documentation that the customer may need. In addition, our service technicians can assist the customer during the execution of the IQ and OQ. As an option, the machines can be supplied in compliance with FDA 21 CFR part 11.