Overview


    our service


    1. Pesticide registration risk assessment
    2. Feasibility analysis of pesticide registration
    3. Pesticide registration test agent
    4. Pesticide registration data writing agent
    5. Pesticide registration data and test report review
    6. Pesticide registration change agent
    7. Pesticide registration continuation agent
    8. Data authorization information service
    9. Original drug source certification information service
    10. Veto analysis and solutions
    11. Registration data submission and approval progress attention


    Our advantage 


    Risk assessment technique
    1. A team engaged in pesticide risk assessment research earlier in China 
    2. Master pesticide risk assessment techniques in Europe, America and China 
    3. Help companies complete a complete set of pesticide registration requirements risk assessment 
    4. Conduct risk assessment during the pilot phase to help companies reduce unnecessary trials and schedule high-level trials in a timely manner

    Registration strategy and risk analysis 
    1. Master the registration data and GLP requirements of major countries in the world to help companies carry out global registration layout 
    2. Accurately determine the product registration category and the corresponding trials that need to be completed before registration
    3. Grasping the latest developments, in-depth analysis of the "Pesticide Registration Management Measures" and "Pesticide Registration Data Requirements" to provide an optimal registration plan
    Arrange the trial reasonably, the quality of the report is checked 
    4. Familiar with the formulation and test arrangement process of drug efficacy and residue 
    5. Understand the problems that are likely to occur in the test report and communicate effectively with the test unit 
    6. Understand the time and cost required for each test to be completed, and arrange the corresponding test reasonably 
    Save registration time and cost 
    7. Accurate use of data reduction rules, writing data reduction applications, avoiding unnecessary trials 
    8. Proficiency in the use of data authorization principles, access to information, saving registration time
    9. Flexible use of the same product identification principles to complete registration in the most economical and efficient form 

    Experienced in registration, familiar with operational practices 
    1. Experienced registration of new pesticides and preparations Complete hundreds of product registrations 
    2. Understand the test arrangement operation process in Shandong, Jiangsu, Zhejiang and other regions

    QSAR predicts toxicity
    1.The first team in China to focus on non-test method services 
    2.Use non-test methods to obtain pesticide active ingredient and impurity toxicity data, saving test cost



    Pesticide registration agent


    1. The whole process of pesticide registration test agent, registration data writing, registration approval progress tracking.
    2. Accurate use of data reduction rules and writing data reduction applications to avoid unnecessary trials.
    3. Proficiency in the use of data authorization principles, access to information, saving registration time and costs.
    4. Flexible use of the same product identification principles to complete registration in the most economical and efficient form.


    Feasibility analysis of pesticide registration


    1. Master the world's major national registration data and GLP requirements to help companies with global registration.
    2. Accurately determine the product registration category and the corresponding tests that need to be completed before registration.
    3. Grasp the latest policy developments, and thoroughly analyze the "Pesticide Management Regulations", "Pesticide Registration Management Measures" and "Pesticide Registration Data Requirements" to provide an optimal registration solution.

    Pesticide registration test agent


    Chemical test, efficacy test, residue test, environmental test, toxicology test, formulation identification, strain identification, etc.

    Pesticide registration authorized agent

    Under the newly revised Pesticide Management Regulations, you will find the authorization materials for the same original drug or the same preparation product for high-quality pesticide products, shortening the registration period and saving capital investment.

    Pesticide registration data writing agent

    The new pesticides and preparations have rich experience in registration, and a large number of product registrations have been completed. The registration materials are clearly written. Understand the review process of the pesticide verification department of the Ministry of Agriculture and Rural Areas and be familiar with the initial review procedures for pesticide registration in the provincial pesticide certification departments.


    Pesticide registration change agent


    1. Expand the scope of use;
    2. Use method changes;
    3. Increase the dose used;
    4. Reduce the dosage used;
    5. The quality specification or composition of the original drug (maternal drug) is changed;
    6. Modification of formulation quality or composition;
    7. The toxicity level is changed.


    Pesticide registration continuation agent


    The applicant should apply for continuation before the expiration of 90 days. If the application has not been extended within the time limit, it shall apply for registration again. At present, there is only one chance for registration renewal. The company pays more attention to it and we will provide you with quality registration and renewal services.


    Original drug source information service



    Provide original drug source information


    Pesticide registration risk assessment


    1. Has a team engaged in pesticide risk assessment research earlier in the country.
    2. Master pesticide risk assessment techniques in countries such as Europe, America and China.
    3. It can help companies complete the pesticide registration risk assessment required by the regulations.
    4. Conduct risk assessments during the pilot phase to help companies reduce unnecessary trials and schedule high-level trials in a timely manner.