35
Providing business consulting services in the field of
regulatory submission management to medical companies to
assist them with applications for medical device approval;
financial record-keeping for regulatory compliance purposes;
business consulting and management in the field of clinical
trials, namely, clinical data and regulatory submission
management on behalf of medical companies to assist them
with clinical research, clinical trials, and applications
for medical device approval
41
Arranging and conducting of educational seminars in the
field of human factors, namely, the usability and ergonomics
of medical devices
42
Medical research; medical research in the field of medical
devices; product development; product development for
others; product research and development services for
others; consulting services; consulting services in the
field of clinical trials of medical and clinical diagnostic
products; consulting services in the field of product design
and development; product design and development in the field
of medical devices and consumer products; product testing;
product quality testing services; product safety testing
services; design and testing of new products for others;
design and testing of new products, namely, medical devices
and consumer products, for others; development of user
instruction manuals for medical devices and consumer
products for others; consulting in the field of human
factors engineering; consulting in the field of human
factors engineering, namely, the usability and ergonomics of
medical devices; consulting in the field of complaint
management systems for clinical trials and medical and
clinical diagnostic products; consulting in the field of
risk analysis for clinical trials and medical and clinical
diagnostic products; product design and development in the
field of medical devices with governmental regulatory
bodies