Basic information
Outline of the system
As a general rule, the importation of products does not require import licences; however, there are some products that require permits, authorizations, certificates and/or approval for importation, for reasons of public safety, animal or plant health, or environmental protection.
El Salvador has the Import and Export Processing Centre (CIEX El Salvador) of the Central Reserve Bank, Import Section, which is the body responsible for centralizing, streamlining and simplifying import and export procedures.
Interested parties can contact the Centre by email: cieximportaciones@bcr.gob.sv; or telephone: (+503) 2281 8000. Some import procedures are available online at: https://www.ciexelsalvador.gob.sv/ciexelsalvador/.
A process to improve governance is under way to reduce response times for products requiring import authorization, provided the required documentation is complete and submitted in advance of importation.
In accordance with Legislative Decree No. 417, authorization must be obtained and the fees must be paid for the licence to import or manufacture chemicals and compounds, pharmaceutical products, fertilizers and preparation for pharmaceutical and cosmetic use, hygiene products and medical imports. The authorization will be issued once the product has been assessed and approved by the regulatory authority.
Product coverage
Chemicals and compounds, pharmaceutical products, fertilizers and preparations for pharmaceutical use and cosmetics, hygiene products and medical inputs
Nature of licensing
Automatic
If Automatic, administrative purpose
Non-Automatic
If Non-Automatic, description of the notified Non-Automatic Licensing regime
Products under restriction as to the quantity or value of imports
The purpose of these licences is not to restrict the quantity or value of imports, but rather to verify compliance with chemical and pharmaceutical product standards for human consumption/use.
Questions for products under restriction as to the quantity or value of imports
Not applicable.
The system applies to products originating from which country?
It applies to all countries, irrespective of the origin of the products.
Expected duration of licensing procedure
Legal requirements
Is the licensing statutorily required?
This type of product is governed by Legislative Decree No. 417, entitled "Fees applicable in the National Directorate of Medicines for services and licences for health establishments".
Does the legislation leave designation of products to be subject to licensing to administrative discretion?
Is it possible for the government to abolish the system without legislative approval?
Eligibility of applicants
Is there a system of registration of persons or firms permitted to engage in importation?
What persons or firms are eligible to apply for a licence?
All persons/importers have the right to apply for import authorizations, whether natural and legal persons, including foreign nationals with a residence permit.
Is there a registration fee?
Is there a published list of authorized importers?
Contact point for information on eligibility
Ministry/Authority
Address
Telephone
Fax
E-mail address
Website
Contact officer
Submission of an application
Administrative body(ies) for submission of an application
Documentation requirements
What information is required in applications?
Importers must be registered in the CIEX-BCR Imports System (SIMP), by following the steps described here: https://www.ciexelsalvador.gob.sv/ciexelsalvador/pasos-para-registrarse-....
They must have a user name and password for the DNM administrative procedures portal. These can be requested electronically by sending an email to: importaciones.exportaciones@medicamentos.gob.sv or in person at the counters in the DNM by completing the form set out in Annex II (a). Information on the importer and the product to be imported is required. For each section by product, the application form is attached.

What documents is the importer required to supply with the application?
The documents required are described in detail for each product in the section entitled "Documentational and other requirements for application for a licence", such as the certificate of free sale or other official document containing the same information, etc.
Window of submission of an application
How far in advance of importation must application for a licence be made?
Prior to importation, so that when the product enters the country, it already has the import licence (permit).
Are there any limitations as to the period of the year during which application for licence can be made? If so, explain
There are no limitations on the date of submission of an application.
Issuing the license
Can a licence be granted immediately on request?
Generally speaking, import permits are granted promptly, provided all documentation is complete.
Can licences be obtained within a shorter time-limit or for goods arriving at the port without a licence
Import licences (permits) are generally issued in an expeditious and timely manner. Work is currently under way on a government improvement process to reduce response times, provided that the required documentation is completed prior to importation.
Which administrative body is responsible for approving application of licences?
The importation of these products can be processed through the single window of the Import and Export Processing Centre (CIEX-BCR).
The importer must be registered in the Imports System (SIMP) of CIEX-BCR.
To import medicines, the importer must apply to the National Directorate of Medicines (DNM) to create a user name and password for the administrative procedures portal, so that the import voucher can be generated, which will then be submitted through the CIEX single window together with the import application.
The import application must be submitted through the CIEX single window, with the supporting technical documentation.
More details about the procedure for requesting authorization to import chemicals and compounds, pharmaceutical products, fertilizers and preparations for pharmaceutical and cosmetic use, can be found at: https://www.medicamentos.gob.sv/index.php/es/66-como-importar.
Must the applications be passed on to other organs for visa, note or approval?
Are there any other conditions attached to the issue of a licence?
No, these products are not subject to quantitative restrictions.
There are no other conditions.
Fees and other administrative charges
Is there any licensing fee or administrative charge?
Yes.
What is the amount of the fee or charge?
Authorization to import chemicals and compounds, pharmaceutical products, fertilizers and preparations for pharmaceutical and cosmetic use, hygiene products and medical inputs is subject to payment of a product-specific tariff, which is set forth in Legislative Decree No. 417. See Annex II (c).

Is there any deposit or advance payment required associated with the issue of licences?
No, none.
Amount or rate?
Is it refundable?
What is the period of retention?
What is the purpose of this requirement?
Refusal of an application
Under what circumstances may an application for a licence be refused other than failure to meet the ordinary criteria?
Authorization is refused only when the established legal requirements are not met.
Are the reasons for any refusal given to applicants?
Applicants are informed in writing.
Have applicants a right of appeal in the event of refusal to issue a licence?
Appeals for review may be filed before the same institution from which the import licence or permit was requested.
If so, to what bodies and under what procedures?
In El Salvador, the Law on Administrative Procedures regulates the administrative review procedure for settling disputes when authorization is refused.
Once administrative remedies have been exhausted, there is also the option of filing a claim before the administrative tribunals, which have jurisdiction to verify the legality of and settle any administrative disputes that might arise between the public administration and individuals.
Importation
Are there any limitations as to the period of year during which importation may be made?
What documents are required upon actual importation?
The import application must be submitted through the CIEX single window, with the supporting technical documentation. Document requirements can be found in the CIEX Guía de importaciones de medicamentos, cosméticos, higiénicos, productos químicos e insumos médicos (Manual for imports of medicines, cosmetics, hygiene products, chemicals and medical inputs), attached in Annex II (b). The approved import licence or permit.

Are there any other administrative procedures, apart from import licensing and similar administrative procedures, required prior to importation?
No, none.
Conditions of licensing
What is the period of validity of a licence? Can the validity be extended? How?
It is generally 30 days. (Phytosanitary, animal health and food certificates) It varies depending on the type of product. The validity of licences cannot be extended, they must be requested again. Consideration will be given to special cases where the goods are in transit and there has been some delay.
Is there any penalty for the non-utilization of a licence or a portion of a licence?
No penalty is imposed for the non-utilization of import licences or permits.
Are licences transferable between importers? If so, are any limitations or conditions attached to such transfer?
Import licences or permits are non-transferable, as they specify the particulars of the importer and the specific product/quantities to be imported.
Foreign Exchange
Is foreign exchange automatically provided by the banking authorities for goods to be imported?
The legal currency in circulation in El Salvador is the United States dollar and the exchange rate is set by the Central Reserve Bank and has been fixed since 2001.