Discusiones de Medical Quality Management Systems (Qms)

For USFDA 21 CFR Is must hence please share whether it is compile regulatory requirement

i need some additional functionality which is presently not in software it is possible?

When do you think a planning tool/Calender can be incorporated in Greenlight Guru? This would be very helpful for planning audits, Capa timelines etc.

1) We have to re-route closed document first to an open phase than we can update it in new web services. But in old web services (CommandManager) , we were able to update document. It is difficult sometime for some document to route back to open phase. 2) Some document is not allowing to re-open... Leer más

In building quality documents you have the field for selecting the system elements where you have ISO 9001:2015, ISO 13485:2003, and others, however, ISO 13485 has been updated to version 2016 replacing 2003.

I prefer to download the file directly

We need to create and simulate and create forms easily in reliance

Can the OOB applications be easy to decipher so that modifications are easily made? Saves time.

Currently Meritor uses a software called IValua for onboarding new suppliers. In addition, it's supposed to collect data to generate supplier ratings. However, it's a "off premise" software and our ETQ Reliance instance is "on premise" since we have Export controlled data. Would like to be... Leer más

Artes respecto estuches y prospectos que usamos en el Laboratorio. Podrian circular para su control dentro del sistema?

Search and Find OMAR Areas Designers Input on what fashoons best with a Man with one eye. Cyborg life

How would you recommend setting up your most recent development released documents versus live active documents. I feel these could be implemented in a clearer way (ie numeric and alpha revisions etc. I have used in previous QMS systems)

I see many opportunities to share, reuse and faster learn from each other to better make medical products.