1 / 1

How to get ISO 13485 certification

Remember that the process of obtaining ISO 13485 certification can be complex and time-consuming, but it demonstrates your commitment to quality and regulatory compliance in the medical device industry. It is essential to involve relevant stakeholders, allocate resources, and continuously improve your QMS to achieve and maintain certification successfully.

siscertification
Télécharger la présentation

How to get ISO 13485 certification

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. How to get ISO 13485 certification Obtaining ISO 13485 certification involves several steps and requires a commitment to implementing and maintaining a quality management system (QMS) that complies with the standard's requirements. Here's a general outline of the certification process: Familiarize Yourself with ISO 13485: First, thoroughly review the ISO 13485 standard and understand its requirements. This will give you a clear idea of what is expected to establish a compliant QMS. Gap Analysis: Conduct a gap analysis to identify the areas where your current quality management system aligns with ISO 13485 requirements and where improvements are needed. Develop and Implement a QMS: Based on the results of the gap analysis, create and implement a QMS that fulfills the ISO 13485 requirements. This may involve updating existing processes, procedures, and documentation. Internal Audits: Perform internal audits to assess the effectiveness of your QMS. Identify and address any non-conformities to ensure readiness for the certification audit. Management Review: Conduct regular management reviews to ensure top management's involvement and commitment to the QMS. Choose a Certification Body: Select an accredited ISO certification body that is authorized to provide ISO 13485 certification. Accreditation ensures the credibility and reliability of the certification process. Certification Audit: The certification body will conduct an on-site audit to assess your organization's compliance with ISO 13485. This audit may be performed in stages, focusing on different aspects of the QMS. Remember that the process of obtaining ISO 13485 certification can be complex and time-consuming, but it demonstrates your commitment to quality and regulatory compliance in the medical device industry. It is essential to involve relevant stakeholders, allocate resources, and continuously improve your QMS to achieve and maintain certification successfully. Unit No – 514, 5th Floor, Sector – 48 Vipul Business Park, Sohna Road Gurgaon, Haryana, 122018 Phone: +91-7011768166, 8860610495 Email: support@siscertifications.com

More Related