MDD (Medical Device Directive) and Medical Device Regulation (MDR) Transitional Provisions
If you have CE marked products in Europe, you may already be aware of the change from the Medical Device Directive (MDD) to the Medical Read More »
Importance of standards conformance is undeniable, unfortunately, so is the complexity of becoming compliant. Conformity Technology provides complete compliance solutions, so you can focus on building great products…
Don’t let the complexity of conformance with standards such as ISO-9001 hold you back! Let us help you with your conformance needs so you can focus on solving world problems…
With over 30 years of experience, we are the experts when it comes to conformance. Contact us to find out how our customized solutions can help you with your conformance needs.
Complex standards that hard to understand and follow
Companies need to focus on their core task: product development
Companies need a partner with a track record that they can trust
Existing solutions have prohibitive costs
Conformance needs to be maintained and recertification is required on a periodic basis
Conformity is with you every step of the way. It provide you the best solutions of your problems, we took care of the core issues (Identity, Maintain, Prepare, Acquire). We are dedicated to provide best of the elite alternatives to overcome those issues and make things more feasible for our users.
Identify certification needs
Develop processes, documents etc. for compliance
Help with every step of compliance audit
Follow changes in standards and update accordingly to maintain certification
Conformity is with you every step of the way. It provide you the best solutions of your problems, we took care of the core issues (Identity, Maintain, Prepare, Acquire). We are dedicated to provide best of the elite alternatives to overcome those issues and make things more feasible for our users.
Identify certification needs
Develop processes, documents etc. for compliance
Help with every step of compliance audit
Follow changes in standards and update accordingly to maintain certification
Conformity is with you every step of the way. It provide you the best solutions of your problems, we took care of the core issues (Identity, Maintain, Prepare, Acquire). We are dedicated to provide best of the elite alternatives to overcome those issues and make things more feasible for our users.
CONFORMITY SOLUTION
Identify certification needs of our client to help them to succeed in long run. We work for:
CONFORMITY SOLUTION
Develop processes, documents etc. for compliance.
CONFORMITY SOLUTION
Help with every step of compliance audit.
CONFORMITY SOLUTION
Follow changes in standards and update accordingly to maintain certification.
If you have CE marked products in Europe, you may already be aware of the change from the Medical Device Directive (MDD) to the Medical Read More »
Continuing with the Quality Management discussion that I started in my last blog, let’s talk about how changes may occur within a predefined process. Perhaps Read More »
A Quality Management System (QMS) is a system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. ISO 9001:2015 defined approach to Read More »
The prefix of the standard provides clues as to which country it originates from. For example, ASTM stands for American Society for Testing and Materials Read More »
Although the ISO 9001 Quality System standard can be used by any industry, ISO 13485 is the go-to Quality System standard widely used (and recognized) in Read More »
Super employee Mitch has left the company! Will we ever be able to find someone to replace him? Probably not immediately. But if his work Read More »
If you have CE marked products in Europe, you may already be aware of the change from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR). Currently, the MDD is no longer but if you have products that are CE marked under the MDD, Article 120 of the MDR may allow you to […]
Continuing with the Quality Management discussion that I started in my last blog, let’s talk about how changes may occur within a predefined process. Perhaps your company has a software development process that it has been using for some time. Someone at your company thinks that the process is too burdensome and would like “streamline” […]
A Quality Management System (QMS) is a system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. ISO 9001:2015 defined approach to QMS is the most commonly used. However, not all processes defined by ISO 9001:2015 may be pertinent to your organization. So, the question is: What are the processes needed for […]