ISO 13485 Certification

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ISO 13485 Certification

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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. – PowerPoint PPT presentation

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Title: ISO 13485 Certification


1
ISO 13485 Certification Quality System for
Medical Device 
  • For details visit Here http//www.ursindia.com/is
    o_13485.aspx

2
ISO 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
3
ISO 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

For details visit Here http//www.ursindia.com/is
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
5
How 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
6
Contact 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/

7
THANK YOU
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