Title: ISO 13485 Certification
1ISO 13485 Certification Quality System for
Medical Device
- For details visit Here http//www.ursindia.com/is
o_13485.aspx
2ISO 13485 Certification
- We provide ISO 13485 certification, an
international standard that defines quality
management system (QMS) requirements for
manufacturers of medical devices. The primary
objective of the standard is to facilitate
harmonised QMS requirements for regulatory
purposes within the medical device sector.
For details visit Here http//www.ursindia.com/is
o_13485.aspx
3ISO 13485 Requirements
- In order to achieve ISO 13485 certification, you
must - develop written policies for the following
functions - Document and record controls
- Internal auditing procedures
- Controls for non-conformance
- Corrective and preventative actions
- Process and design controls
- Record retention
- Accountability and traceability
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o_13485.aspx
4 Planning the Quality System
- ISO 13485 Standard includes a requirement for
Quality Planning. Writing a Quality Manual is not
sufficient to meet this requirement. You need
documented Quality Plans for implementing changes
to your Quality Management System, and creating a
new Quality System from scratch is a big change.
There is no required format for quality plans.
Spreadsheets and Gantt Charts are the most common
tools for quality planning.
For details visit Here http//www.ursindia.com/is
o_13485.aspx
5How is ISO 13485 recognized worldwide?
- ISO 13485 focuses on the harmonization of the
Quality Management Systems in the framework of
Medical Device regulatory requirements. It is not
surprising to see that many jurisdictions
recognize or even require that Medical Device
manufacturers obtain ISO 13485 certification in
order to access their market.
For details visit Here http//www.ursindia.com/is
o_13485.aspx
6Contact details
- NOIDA HEAD OFFICE
- F-3, Sector 06 Noida- 201 301,NCR Delhi,
IndiaTel-91-120-6404223 - 26,Tel91-9971853337
,Fax91-120-4297916E-info_at_ursindia.com - W-http//www.ursindia.com/
7THANK YOU