Quality
PRP Quality Systems
PRP Optoelectronics has an established history of Quality covering our
Design, Development and Manufacturing activities. Our operations have been
independently inspected and approved via regular third party assessment
by the British Standards Institute (BSI).
From our beginning in 1989, PRP was registered to AQAP-1, and in 1993
our Quality Management System (QMS) evolved to meet the requirements of
ISO 9001: 1994. We subsequently upgraded our systems to comply with the
current International Quality Standard, ISO 9001: 2000.
Alongside our ISO 9001: 2000 Certification, PRP also hold approval for
the production of Medical Devices through BSI assessment against EN46002,
ISO 13485: 2003, and MDD 93/42/EEC Annex V, Section 3.2. Our light sources
and associated electronic control systems for Medical Products thereby
carry the CE mark.
In our daily operations, PRP maintain appropriate Quality Management Systems
to support the requirements of all of our customers.
Quality System Certification and Scope
Our BSI Certification of Registration to ISO 9001: 2000 bears the UKAS
Accreditation mark for the activities detailed in the following scope:
Design, development and manufacture of solid state technology devices
for the emission, detection and control of visible and infra-red radiation,
including display modules and sub-systems using optoelectronic devices
integrated with electronic drive circuitry.
From assessment by BSI, PRP hold EC Certification enabling the CE mark
to be affixed to our medical devices in respect of:
The manufacture of light sources and associated electronic control
systems for medical purposes.