Jasa Pembuatan SKIP (Surat Keterangan Informasi Produk) Resmi – di PT Multi Jasa Berjaya
Our Services – Fast & Trusted Official Legalization
At PT Multi Jasa Berjaya, we assist in the preparation and submission of SKIP (Surat Keterangan Informasi Produk) for the registration of medical devices (AKL/AKD) and household health supplies (PKRT). We ensure your documents meet the standards set by Indonesia’s Ministry of Health and are ready for submission to the e-Registration system.
What is SKIP (Product Information Letter)?
SKIP is an official letter issued by the Ministry of Health of the Republic of Indonesia that clarifies whether a product falls under the classification of a medical device or household health product (PKRT).
This document is especially useful for importers and businesses to: Avoid importing unregistered or misclassified products, Fulfill regulatory requirements & Ensure proper product supervision according to Indonesian laws
Required Information for SKIP Application
- Product Name
- HS (Harmonized System) Code
- Product Function
- Instructions for Use
- Additional Notes (if applicable)
Why Choose Us?
Experienced in SKIP Documentation (We’ve handled a wide variety of SKIP applications for imported medical devices and household health products), Fully Compliant Format (Our documentation is prepared to align with official MoH templates) & Fast Processing (Ready for submission to the MoH e-registration system without delays).
FAQ – Frequently Asked Questions
- When do I need a SKIP?
You need a SKIP when your product's classification is unclear (i.e., whether it is considered a medical device or PKRT) and you want to import or register it in Indonesia. The SKIP provides formal clarification from the Ministry of Health. - Who must apply for SKIP?
Importers, distributors, or product owners who are preparing for AKL, PKL, or PKRT license applications, and require confirmation of product classification. - Is SKIP only for medical devices and PKRT?
Yes. SKIP is typically used for products that might fall under medical device or PKRT regulations, to ensure correct classification and oversight by the MoH. - Is SKIP mandatory?
Yes, if the classification of your product is unclear, or if requested by regulatory authorities during the licensing or product entry process.
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