KBLI 21012

MANUFACTURE OF PHARMACEUTICAL PRODUCTS FOR HUMAN

This group includes businesses in the manufacture and processing of pharmaceuticals, health supplements, in the form of preparations for humans, for example in the form of tablets, capsules, ointments, powders, solutions, parenteral solutions and suspensions, antiseptic soaps and surgical threads. Including the contraceptive products industry for external use and hormonal contraceptive drugs, the medical diagnostic equipment industry, including pregnancy testing, the radioactive in-vivo diagnostic substances industry, the biotechnology pharmaceutical industry and the medical dressings industry, bandages and the like and cosmetic cotton.

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Key requirements to set up a manufacture of pharmaceutical products for human in Indonesia

The following requirements are based on the Indonesian business classification code 21012

Maximum foreign ownership
0%
Minimum capital
Rp. 0 billion
Local SME partnership required
No

What is a KBLI 21012?

A KBLI is an Indonesian business classification, last revised in 2020. The KBLI determines the regulations for a specific business activity.

21

Division

0

Group

1

Class

2

Indonesian class

21012 stands for manufacture of pharmaceutical products for human

What are the requirements to set up a manufacture of pharmaceutical products for human in Indonesia?

Shareholders

  • This business classification does not allow foreign ownersip.

The process of registering manufacture of pharmaceutical products for human company in Indonesia

The exact process of registering a manufacture of pharmaceutical products for human company depends on the location of your company's registered address.

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