Design Control SOP - Streamlining with R&D Department

Hi folks.

I'm a newly registered user of the forum and fairly new to the Quality realm. I was looking for tips or samples of SOPs for Design Control (7.3 of ISO-13485) which are more user-friendly for R&D types.

Our company uses an off-the-shelf SOP which is too cumbersome to be of much practical use. Any ideas or samples would be very much appreciated!!

It is a bit depends on your business ...

Thanks. It is a small medical device manufacturer. We have several products on the market and a small R&D team developing enhanced products based on customer and market feedback and new products based on the same.

I do not believe in golden template.
I would suggest, to interpret what is in the standard according to your view and, well, write it down, review with expert and let it go.
Really, I do not think there would be any template you could use.
Alternative is to hire a consultant for this job. Could be a weekly cost as far as I would commit (but I can not, anyway).
Regards!

Thanks again. I am doing that. I'd just like to get some ideas and useful templates from others if possible, to incorporate into our own.

I have moved this post to ISO 13485 and ISO 14969 - Medical Devices - Quality Management Systems sub-forum, for better hits and responses ....

Well, I guess you ask it with reason, if there is any concern you have or specific uncertainty, just let us know.