What do you need to know?
Orthopaedic establishments and orthopaedic sections of pharmacies in Catalonia must obtain operating authorization from the Department of Health.
These establishments offer orthopaedic medical products, such as prostheses and orthoses, intended to compensate for the loss of autonomy, functionality, or physical capacity of users.
Attention: If orthopaedic medical products made to measure according to the prescription of a specialist, with characteristics designed for a specific patient, are dispensed, this is not the correct procedure. In this case, authorization must be requested from companies manufacturing custom orthoprosthetic health products.
This procedure can only be done online. Any documentation you provide through another channel will not be considered and will not be valid for the purposes of the submission date.
Specific forms have been enabled for requests or communications for this procedure, which are mandatory to use. You can download them from this page, and it is important to always use the latest version. If you submit the request or communication using other forms, they will be considered not submitted.
Authority responsible
For individuals or legal entities who own orthopaedic establishments or pharmacy offices with an orthopaedic section where these products are not custom-made.
You can submit the application at any time, but keep in mind:
- Substantial modifications: You must obtain prior authorization from the Department of Health before making the modification.
- Non-substantial modifications: You have a period of one month to communicate the modification made.
The documentation you must attach to the application varies according to the type of modification:
For relocation, expansion of premises, and structural changes in the facilities that imply expansion, redistribution, or restructuring of the facilities.
- Plan of the establishment, issued and signed by the competent technician.
For change of technical director:
- Annex: responsible declaration of the technical director.
- Title or official documentation accrediting the professional exercise of the technical director with a minimum of three years of experience as of May 14, 1999. Documents that serve to accredit professional competence:
- Declaration indicating the establishment of the activity communication, carried out according to Royal Decree 414/1996, of March 1, which regulated medical products, where the person who wants to obtain recognition as a technical director was listed as the responsible technician.
- Certification from the General Treasury of Social Security, or the mutual society to which they were affiliated, indicating the company, the labour category (contribution group), and the period of employment.
- Copy of the employment contract or certification from the company where the work experience was acquired, specifying the duration of the contract periods, the activity performed, and the time interval in which the activity was carried out.
- Have the operating authorization as an orthopaedic establishment or section, issued by the Department of Health.
- Maintain compliance with the necessary requirements for the operating authorization.
- In no case can orthopaedic medical products made to measure according to the written prescription of a specialist, with characteristics designed for a specific patient, be dispensed. In this case, authorization must be requested for companies manufacturing custom orthopaedic products.
Types of modifications:
- Modifications that require prior authorization (substantial modifications):
- These modifications cannot be initiated until authorization has been granted.
- Include:
- Change of ownership of the establishment.
- Expansion, restructuring, or redistribution of the establishment.
- Relocation of premises.
- Modifications that only require communication (non-substantial modifications):
- These modifications can be carried out once the communication has been submitted.
- The communication must be submitted as soon as they occur.
- Include:
- Change of company or establishment name.
- Change of establishment address for administrative reasons.
- Change of social address.
- Change of technical director.
Steps to follow
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1
Step one
Report and/or apply for
This procedure can only be done online.
If you are a legal entity, to submit the form you will need a digital representation certificate. If you act on your own behalf, you can use idCAT Mobile or a digital certificate.
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2
Step two
Check the status of the procedure
You can do it at:
You can do it at:
- In the Private Area (with idCAT Mobile or digital certificate)
- In the Status of my procedures (with the procedure identifier code and your NIF/NIE).
- Phone 012 (with the procedure identifier code and your NIF/NIE).
Check more information on How to monitor and check the status of a procedure.
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3
Step three
Pay the fee
Once you have submitted the form, if the requested modification is subject to a fee, you will find the documentation for payment in your Private area of Canal Empresa (this may take a few hours or [...]
Once you have submitted the form, if the requested modification is subject to a fee, you will find the documentation for payment in your Private area of Canal Empresa (this may take a few hours or days).
You can make the payment:
- With a bank card (VISA or MASTERCARD)
- With a payment letter
Consult all the information on how to pay a procedure.
You must make the payment of the fee to continue the procedure.
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4
Step four
Submitting documentation
Once your application has been reviewed, the Administration may request additional documentation. You can submit it through:
Once your application has been reviewed, the Administration may request additional documentation. You can submit it through:
- Private Area(using idCAT Mobile or digital certificate)
- Status of my procedures(using the transaction identifier code and your DNI/NIF)
Check the video tutorial on how to submit documents for a request.
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5
Step five
Receive response from the Administration
When will I receive the response?
When will I receive the response?
It depends on the type of modification:
- Modifications that do not require authorization (non-substantial modifications): The procedure is considered completed at the time of submitting the communication.
- Modifications that require authorization (substantial modifications): The Administration has a maximum period of one month, counting from the date of entry of the application, to issue and notify the authorization resolution. If this period elapses without an express resolution, the application will be considered approved by administrative silence.
How will I receive the response?
You will receive the notification through the e-NOTUM system.
Can I file an appeal?
Yes, you have one month to file an appeal. The appeal must be addressed to the Secretary General of the Department of Health.