Validation of the Sealing Machine Process for Surgical Packs

Author:

Arredondo-Soto Karina Cecilia1ORCID,Solís-Quinteros Maria Marcela1,Miranda-Ackerman Marco Augusto1,Blanco-Fernàndez Julio2

Affiliation:

1. Universidad Autónoma de Baja California, Mexico

2. Universidad de la Rioja, Spain

Abstract

A manufacturing plant in Tijuana focused on providing medical device solutions to improve the quality of life of patients. The company has developed thanks to its innovative products in the market considerably. As a business strategy at the corporate level, opportunities were detected and involved the transfer of the manufacturing of products to different facilities in Mexico. In order to manufacture a product that complies with standards to ensure the sterile barrier standards to ensure sterilization barrier of the product, this project consists of validating the Max Tray Sealer machine of the kit kat two production lines. The validations process covers all the quality system requirements governed under the ISO-13485 standards, which define the validation stages. The stages of the validation include the installation qualification, the operational qualification, and the performance qualification.

Publisher

IGI Global

Reference19 articles.

1. A Plan-Do-Check-Act Based Process Improvement Intervention for Quality Improvement

2. Creation of Technology-Based Companies: Challenges to Innovate in the Manufacturing Sector of Medical Devices, the Case of Baja California, México

3. Avanos. (2018). About Avanos Leadership. https://avanos.com/about- avanos/#leadership

4. Badii, M. A. (2011). Daena: International Journal of Good Conscience.http://www.spentamexico.org/v6-n1/89a105.pdf

5. Cornejo, M. A. (2010). Control Estadístico de Procesos como Herramienta para la Validación de Procesos (Tesis de pregrado). Universidad Nacional Autónoma de México, Facultad de Estudios Superiores, Mexico, D.F.

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