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SCLERODERMA CLINICAL TRIALS CONSORTIUM, INC. (the SCTC) APPOINTMENT OF MEMBERS PROXY I have been designated by the SCTC Member identified below (the Member) to serve as the Members Coordinating Investigator

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Who needs scleroderma registry amp repository?

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Patients diagnosed with scleroderma who want to contribute their data for research purposes

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Researchers and healthcare professionals studying scleroderma and looking for data to analyze

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What is scleroderma registry amp repository?

The scleroderma registry and repository is a centralized system for collecting and storing data about individuals diagnosed with scleroderma, facilitating research and improving understanding of the disease.

Who is required to file scleroderma registry amp repository?

Healthcare providers who diagnose and treat patients with scleroderma are typically required to file data with the scleroderma registry and repository.

How to fill out scleroderma registry amp repository?

To fill out the scleroderma registry and repository, healthcare providers must complete a standardized form that includes patient demographic information, clinical data, and other relevant medical history.

What is the purpose of scleroderma registry amp repository?

The purpose of the scleroderma registry and repository is to gather comprehensive data to enhance research, improve patient care, identify patterns in the disease, and promote awareness.

What information must be reported on scleroderma registry amp repository?

Information required includes patient demographics, clinical diagnosis, treatment regimens, disease progression, and any related comorbidities.

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