Click me
Transcribed

Quality Management System for Pharmaceutical Companies

TIPS FOR ISO 13485 QUALITY MANAGEMENT SYSTEMS M ISO 13485 1.FREQUENCY Technicians should review their QMS twice per year based on the size and scope of the project. 2.KPIS Each business will have their unique set of key performance indicators. These factors will opt the management process. 3.TECHNOLOGIES Make sure to use advanced quality management software for medical device procedures. It makes tracking easier. 4.ACCESSIBILITY Ease of use & accessibility two of the most important factors to look for when choosing QMS software. 5.OBJECTIVES Effective management reviews are based on agendas. This will help members to keep track of the progress. 6.REVIEW Follow the activities of ISo audits by providing objective *** evidence. If necessary, hire professional auditors. Easy Document collaboration control le Ben Customer satisfaction Efficient Proactive training solutions THIS INFOGRAPHIC IS PRESENTED BY CONTTACT US [email protected] Lumin Logic O Mon-Fri 9.00 AM - 5.00 PM Y Morrisville, NC nefit

Quality Management System for Pharmaceutical Companies

shared by infoluminlogic on Sep 22
0 views
0 shares
0 comments
Our experts have in-depth expertise in all types of medical device regulatory works. Also, they will help you to focus on customer safety and ensuring the products fulfill the safety requirements.

Category

Business
Did you work on this visual? Claim credit!

Get a Quote

Embed Code

For hosted site:

Click the code to copy

For wordpress.com:

Click the code to copy
Customize size