Hi all,
This is my first post, and I hope that all you experienced people can offer me some input.
I am the one-"man" QA/RA in a small (25 people) IVD company in Europe and often need to review regulatory requirements when our sales people are considering new markets.
I have stumbled upon the Clinivation World View, and obtained a sample report from them, which seems very competent.
Do any of you have any insight to offer regarding the validity of the information in the Clinivation reports?
Best regards
Camilla
This is my first post, and I hope that all you experienced people can offer me some input.
I am the one-"man" QA/RA in a small (25 people) IVD company in Europe and often need to review regulatory requirements when our sales people are considering new markets.
I have stumbled upon the Clinivation World View, and obtained a sample report from them, which seems very competent.
Do any of you have any insight to offer regarding the validity of the information in the Clinivation reports?
Best regards
Camilla