The approaches and protocols are available on the homepage of the ministry of health, consumption and welfare section profesionales-farmacia:
Since 1 july 2019 it must follow these new â criteria â and to present all requests for treatment in these protocols that are designed to be directly enforceable before printing.
The request of the treatment to the advisory committee should be carried out by completing the protocols of start-up and specified in models, and attachments containing all parameters to assess that authorisation criteria and renewal of treatment. It should be attached, together with the beginning, patients' informed consent duly filled in. The absence of the completion of each and every one of the requested data can be a negative report for the commencement or continuity of treatment with growth hormone .
- The request of the beginning of treatment
- The follow-up
- Informed consent