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ICMED 13485 QCI Certification for Medical products consultancy by GQS

CE for Medical products

CE for Medical products

With the launch of Medical Product Regulations since 2017, all medical products falling under

CLASS 1, CLASS2 and CLASS 3 shall have to undergo certification to Quality Council of India QCI accredited ICMED Indian Certification for Medical devices.

The legal requirements will be in force w.e.f 2018 and shall comply to all the specifications and requirements for factories manufacturing, trading or supplying medical products falling under CLASS 1, CLASS 2 or CLASS 3 type.

QCI has launched ICMED in 3 categories for certification

  • ICMED 9000 –  based upon ISO 9001  plus additional requirements
  •  ICMED 13485  — based upon ISO 13485  plus additional requirements
  • ICMED 13485 Plus  – based upon ICMED 13485 pluS Product specifications prescribed by MoH

All organisations supplying, trading or manufacturing have to mandatorily achieve certification by QCI accredited Notified body.

GQS was one of the first to attend major seminars on this subject and has been in the field of Medical product certification since 2001 and registered by QCI since its inception.

Drop in an email to SHAKTI@GQSINDIA.COM or RAJ@GQSINDIA.COM to know more details about ICMED, QCI, Certification, Consultancy, ISO 13485.

Assistance regarding ISO certification to all kinds of industries


From engineering, banking, food to hospital assistance for all

All can get guidance to get their ISO certification done in a moment.

All you have to do is to come to General Quality Service, one of the largest and prominent firms of India and just relax. Do not be anxious; they will take care of all your problems.

With their service all around India ISO certification became child’s play for everyone. Their service provision includes almost every field: – Service Industries, Pharmaceutical, Banking, Engineering, Food, Hospital, Education and Software and Chemical Industrial sectors. Not only this, they also furnish your systems through designing the formats and framing the quality procedures and manuals.


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