Existing Chemical

The evaluating standard for standard registration

 

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The acceptance for the data

 

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Designated List of Existing Chemical Substances

    • Guidelines

      OECD 423

 

    • Test system

      SD rats

 

    • Test Aims

      Evaluating the lethal dosage and LD50 of the chemicals through oral route to intake into the body.

 

    • Lead time

      8 weeks

  • Guidelines

    OECD402

  • Test system

    SD rats

  • Test Aims

    Evaluating the lethal dosage and LD50 of the chemicals through dermal route to intake into the body

  • Lead time

    8 weeks

  • Guidelines

    OECD 403

  • Test system

    Wistar rats

  • Test Aims

    Evaluating the lethal dosage and LD50 of the chemicals through inhalation route to intake into the body and observing the effects on lung and/or organs

  • Lead time

    4 months

  • Guidelines

    OECD 407

  • Test system

    SD rats

  • Test Aims

    The chemicals was fed orally for 28 day through three different (low, medium and high) dosage. To evaluate the change in the organs and toxicity after repeated feeding.

  • Test items included

    clinical symptoms, incidence, mortality, fundoscopy, body weight, feed consumption, feed utilization, hematology, serum biochemistry and electrolytes, urology, organ weight, macroscopic and pathological observations, etc. Finally, the results will present as the no observed adverse effect level, NOAEL.

  • Lead time

    7 to 10 months (pre-test was contained)

  • Guidelines

    OECD 408

  • Test system

    SD rats

  • Test Aims

    The chemicals was fed orally for 90 day to evaluate the long-term chronic toxicity. A longer feed period will better to understand the damage on specific tissues and organs. The three different (low, medium and high) dosage were used. To evaluate the change in the organs and toxicity after repeated feeding.

  • Test items included

    clinical symptoms, incidence, mortality, fundoscopy, body weight, feed consumption, feed utilization, hematology, serum biochemistry and electrolytes, urology, organ weight, macroscopic and pathological observations, etc. Finally, the results will present as the no observed adverse effect level, NOAEL.

  • Lead time

    12 to 14 months (pre-test was contained)