Regulated Industries

CRO Group training programs for regulated industries run the spectrum from a one or two hour seminar on a specific requirement to one or two days on the entire EU Medical Device or IVD Directive, the FDA Part 11 (21 CFR 11) Regulation, and or establishing an Internal Audit program addressing ISO 13485:2003  and QSR, Canadian Medical Device Regulation, and EU MDD.

When you arrange a CRO Group training, you're in good company.  CRO Group has conducted training programs for RAPS, Advamed, ASQ, and AAMI.

We offer standards and regulation training programs including:

ISO 13485                    QSR                    Part 11/GAMP5

ISO 14971                    EU MDD/IVDD      Risk Managerment

The Process Approach     CMDR                Internal Auditing

You can select a single topic or combine as many as are applicable to you.

To find out more, click here.