Manufacturing Rules for the Medical Devices in India

Posted on August 2, 2011. Filed under: GHTF, GMP, india, ISO, ISO 13485, learn for free, medical devices, orthopedics, sampling plan for the medical devices, USFDA |

REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

Free download for the educational and noncommercial purpose only

These are the requirement from the Indian government to setup the shop in India.

India has the potential for the growth and has many good suppliers and cheaper labour.

The cost of production of the medical devices is very low as comparable to the other countries.

Only we need to conform to the rules mentioned in the MIII schedule of the GMP.

For Entire Indian GMP, please refer to the next post.

If you require any further information, comment below.

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