Intake and Initial Training We use this information in order to: We
process
(i) complete intake and account Onboarding and
setup processes; (ii)
configuration necessary
initial training performance
Intake,
Initial
Data:
provide Training Information as
As part of the intake, onboarding,
onboarding,
assistance,
for
of
the
our
setup
and
initial
training
and
processes associated with the
Services and the Products, we
regarding the technical operation of contract with you and for
the Products and Services; (iii) our legitimate interests in
may
information provided by you or
generated during such
collect
and
process
deliver
technical
support
and providing,
maintaining,
troubleshooting; (iv) document and and
improving the
manage support and onboarding Services.
interactions. This may include
contact and scheduling details,
interactions;
onboarding, support, and service related data is processed
operations; and (vi) comply with in this context, such
and processing is based on
(v)
improve
our To the extent that health-
account
identifiers,
basic
demographic
information,
applicable
regulatory
safety,
quality,
device,
App
and
data,
and
Platform
technical
documentation your consent. You may
withdraw your consent at
configuration
identifiers,
requirements.
records
of
Such information may be stored, any time; however, please
analyzed, and managed using note that withdrawal of
internal systems and third-party consent may limit our
service providers (such as helpdesk, ability to provide certain
communications with our support
or onboarding teams (including
call
notes,
tickets,
or
correspondence). Depending on
the context and the information
you choose to share, this may
CRM, or support management Services
or
support-
platforms), in accordance with this related functionalities, and
Privacy Policy and applicable law.
does not affect processing
activities lawfully carried
also
include
health-related
information provided in the
course of setup, guidance, or
technical assistance.
out
prior
to
such
withdrawal.
Regulatory,
Safety
and We use this information to: (i) Processing is necessary
Medical Event Reporting Data assess, document, investigate, and for compliance with legal
(Vigilance and Post-Market respond to adverse events, safety obligations applicable to
Surveillance):
signals, and regulatory incidents; (ii) medical
device
and,
comply with applicable medical manufacturers,
As part of our obligations as a
medical device manufacturer, we
may collect, process, and retain
information relating to safety,
regulatory, quality, and medical
device
including reporting obligations to is involved, for reasons of
competent authorities, notified public interest in the area
bodies, or regulatory agencies (such of public health and
as FDA or EU authorities); (iii) ensuring high standards of
maintain and improve the safety, quality and safety of
performance, and quality of the medical devices as well as
Products and Services; (iv) conduct for the establishment,
post-market surveillance, vigilance exercise, or defense of
activities, and corrective or legal, as applicable.
preventive actions; and (v) maintain
legally required records and
documentation.
laws
and
regulations, where health-related data
events
Products and the Services. This
may include reports or
notifications concerning adverse
events, serious incidents,
suspected device malfunctions,
safety complaints, technical
issues with potential clinical
impact, product deficiencies,
associated with
the
usage deviations, and other
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