CEIm

The CEIm of the Alicante – General Hospital Health Department will evaluate

• Any clinical trial involving a medicinal product for human use or a medical device submitted for evaluation and intended to be conducted in any hospital within Spanish territory, as well as any amendments to such trials.
• Observational studies involving medicinal products that are submitted for evaluation.
• Other observational studies submitted to the committee for evaluation.
• Other types of studies (e.g., research involving biological samples) in which ethical considerations are particularly relevant and which are submitted to the Committee for evaluation.
• Research projects that require CEIm evaluation.
• Requests for authorization of Biobank samples.

CEIm Registry

• To register all project and/or clinical study documentation submitted to the CEIm.
• To address the Committee’s requests for corrections.

CEIm

• To register all project and/or clinical study documentation submitted to the CEIm.
• To address the Committee’s requests for corrections.
• Other matters not related to registration.