Back to Results
First PageMeta Content
Medical equipment / Medical technology / Product certification / Clinical research / Pharmaceutical industry / CE mark / Notified Body / Medical device / Medicines and Healthcare products Regulatory Agency / Medicine / Technology / Health


Requirements for notified bodies
Add to Reading List

Document Date: 2013-11-01 11:20:25

Open Document

File Size: 118,66 KB

Share Result on Facebook

Company

Notified Body Operations Group / Requirements (A) Resources / EEC / /

Country

United Kingdom / /

Event

Product Issues / Product Recall / /

IndustryTerm

quality system audits / liability insurance policy / appropriate professional indemnity insurance / consultancy services / implantable medical devices / sterile medical devices / adequate insurance cover / manufacturing control / methodology/technology / in vitro diagnostic medical devices / diagnostic medical devices / /

Organization

Medicines & Healthcare Products Regulatory Agency / MHRA / Medicines and Healthcare Products Regulatory Agency / /

Position

General / designer / Secretary of State / authorised representative / /

Product

certificates / /

URL

http /

SocialTag