Indonesia is attempting to simplify regulations by reducing the time needed for review, promoting easier access for license application and to develop the local manufacturing sector.
New Registration Timeline
Indonesia is launching Digital signature system in January 2019. This will allow marketing license approvals to be signed electronically and will not require any stamp and direct signature.
Implementation on Medical Device Import Trade Control
Setting Up Medtech Business in Indonesia
GMP Compliance
Above is a figure shared in Indonesia MoH latest update. By increasing the number of facilities to be audited, it can ensure that a wider range of medical devices will be manufactured to the highest quality possible to protect the health and safety of the end-users.
The Indonesian Ministry of Health has also implemented a medical device import trade control to control the quality of the medical devices being imported as well as to promote the competitiveness and develop the local manufacturing industry.
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