Solve rare diseases in the front end
Early detection, early diagnosis
and early intervention

AI Solution for Rare Disease Research
Solve rare diseases in the front end Early detection, early diagnosis and early intervention
AI Solution for Rare Disease Research
AI Solution for Rare Disease Research

Background

In recent years, national policies on rare diseases has been issued frequently, and great emphasis has been placed on the registration and related processing of rare disease diagnostic and treatment information.
The establishment of an information system to collect relevant data facilitates the understanding of the epidemiology, clinical diagnosis and treatment, and also the status of medical insurance of rare diseases in China. The information system also provides scientific basis for formulating population intervention strategy, improving the system of diagnosis and treatment services, improving the standards of medical insurance of patients, and improving drug accessibility.
Difficulties in the clinical diagnosis, treatment and scientific research of rare diseases
  • Detection

    It's not uncommon
    But it's hard to find out
    Often overlooked
  • Diagnosis

    It is difficult to diagnose due to the involvement of many disciplines
    There is a general lack of professional knowledge of rare diseases
    High rate of misdiagnosis and missed diagnosis
  • Treatment

    It is difficult to use drugs accurately
    More than 7000 rare diseases are known, but only 10% of them have a treatment plan
    More than 700 rare diseases have been well-defined, yet 95% of them have no specific drugs
  • Research

    Registration of rare diseases started later than foreign countries
    There is a severe lack of data for research
    The research is of great value

Background

In recent years, national policies on rare diseases has been issued frequently, and great emphasis has been placed on the registration and related processing of rare disease diagnostic and treatment information.
The establishment of an information system to collect relevant data facilitates the understanding of the epidemiology, clinical diagnosis and treatment, and also the status of medical insurance of rare diseases in China. The information system also provides scientific basis for formulating population intervention strategy, improving the system of diagnosis and treatment services, improving the standards of medical insurance of patients, and improving drug accessibility.
Difficulties in the clinical diagnosis, treatment and scientific research of rare diseases
  • Detection

    It's not uncommon But it's hard to find out Often overlooked
  • Diagnosis

    It is difficult to diagnose due to the involvement of many disciplines
    There is a general lack of professional knowledge of rare diseases
    High rate of misdiagnosis and missed diagnosis
  • Treatment

    It is difficult to use drugs accurately
    More than 7000 rare diseases are known, but only 10% of them have a treatment plan
    More than 700 rare diseases have been well-defined, yet 95% of them have no specific drugs
  • Research

    Registration of rare diseases started later than foreign countries
    There is a severe lack of data for research
    The research is of great value

Solution

Based on the advantages of data and intelligent application platform knowledge base system, BaseBit has launched an intelligent solution for the integration of clinical research on rare diseases. It is a multimodal and multidimensional AI solution integrating diagnosis and treatment registration of rare diseases, data mining, research and analysis, output of scientific research value and diagnosis and treatment plan. This solution highly conforms to the needs of medical workers, government departments and researchers to perform their jobs, thus providing research value, sharing value and clinical value.

Solution

Based on the advantages of data and intelligent application platform knowledge base system, BaseBit has launched an intelligent solution for the integration of clinical research on rare diseases. It is a multimodal and multidimensional AI solution integrating diagnosis and treatment registration of rare diseases, data mining, research and analysis, output of scientific research value and diagnosis and treatment plan. This solution highly conforms to the needs of medical workers, government departments and researchers to perform their jobs, thus providing research value, sharing value and clinical value.

Program Advantages

    • Improve the standards of diagnosis and treatment of rare diseases
    • Support the decision-making power of health management
    • Improve the ability of sequencing analysis
    • Improve the ability of report interpretation
    • Enhance academic influence
    • Deliver scientific research value

Program Advantages

    • Improve the standards of diagnosis and treatment of rare diseases
    • Support the decision-making power of health management
    • Improve the ability of sequencing analysis
    • Improve the ability of report interpretation
    • Enhance academic influence
    • Deliver scientific research value

Scheme Flow Chart

Scheme Flow Chart

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