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Contract review: The contract will be reviewed according to requirement of R&D service from the sponsor, based on actual situation, and in aspect of resources allocation (personnel arrangement and material preparation) required to fulfill the task on schedule.

Sponsor relevant material preparation: The sponsor shall prepare the test substance, reference substance and their COAs and MSDSs, and submit written testing application to the test facility management.

Sample and study allotment of Lab:The test facility management will allot the study director according to the test schedule, and transfer the test substance, reference substance and their COAs and MSDSs to TSCO for storage.

Propose the draft study plan:The study director will propose the draft study plan according to test application and submit the draft study plan to QA and sponsor for review.

Conduct experiment:The experiment will be started after the approval of the study director. The QA will supervise the entire experiment procedure.

Data verify and propose the draft report and review of the report:The study director will review the test data, propose the draft report and submit the draft to the QA and sponsor for review.

Finalize the report:The study director will sign on the final report. The raw data generated from the test and one copy of the final report will be archived for 15years. The other copy of the final report will be submitted to the sponsor.

Contract Review:After winning the bidding, the sales department will submit the business requirement to the team leader of testing work group. Then the team leader will call up all the team members to review the contract in aspect of the task type, workload, detailed requirement from the sponsor, and resources allocation (personnel arrangement and material preparation) required to fulfill the task on schedule.

Sample Testing Schedule:Quality assurance unit together with sales department will make a sample testing schedule according to the time node, technical requirement and etc. confirmed on contract review.

Sampling:Sample department personnel will go to the site for sampling according to sample testing schedule. The storage and transportation should meet the corresponding storage requirement (temperature and humidity and etc.) and be kept relevant record.

Businesses Reception and Sample Preparation:When the sample arrives at the lab, the business acceptance specialist will first check the sample and record the relevant information. Then he/she will arrange and allot the testing items according to the sampling plan and at the same time submit the sample to sample department for sample preparation.

Test and Issue the Original Record:The test will be conducted in the lab. Each batch of the test includes several quality control methods such as duplicate samples, quality control sample, standard recovery, blank test and etc.. The quality control of test result and confirmation of positive samples flow will be executed in accordance with relevant document and the original record will be kept.

Report Propose and Approval:Report department personnel will propose the report. QA will review the report and the authorized signatory will approve the report.

Data Submit and Report Analysis:Summarize and submit (upload to system etc.) the data in accordance with the client and make sure its accuracy and timeliness. Propose an analysis report if necessary.

Contract review:The contract will be reviewed according to requirement of the client, the turkey solution of choosing and customizing testing method suitable for specific food matrices, review and training, and in aspect of resources allocation (personnel arrangement and material preparation) required to fulfill the task on schedule.

Testing Item Determination:Determine the testing items according to the product or enterprise standard, or evaluate or design the solution.

Method option or Development:According to product matrix properties, suitable testing method will be adopted or the method will be developed as requested.

Proposal Determination:concern about the .

Method Validation:Method validation should be done for method development and its applicability should be confirmed.

Testing and analysis of the sample and turkey solution Execution:After confirmation of method applicability or completion of method research and method validation, the sample will be tested and analyzed. At the same time, the turkey solution will be proceeded with.

Quality and Technical Management Review:The quality and technical management is responsible for providing quality assurance and technology checking of overall method R&D, method validation and sample analysis, and reviewing the data generated.

Submit Data Report:Submit the data and test report which is reviewed by the quality and technical management along with the summary report of the turkey solution.

Contract review:The contract will be reviewed according to requirement of R&D service of the client, based on actual situation, and in aspect of resources allocation (personnel arrangement and material preparation) required to fulfill the task on schedule.

Project Established:According to client requirement, the R&D project will be established, or the solutions will be evaluated, including developing liquid and gas phase method, supply of impurity standard substance (Synthesis or preparation) and analysis of the structure of the impurities.

Project Execution:After confirmation of method applicability or completion of method research and method validation, the sample will be tested and analyzed. At the same time, the turkey solution will be proceeded with.

Quality and Technical Management Review:The quality and technical management is responsible for providing quality assurance and technology checking of overall method R&D, method validation and sample analysis, and reviewing the data generated.

Submit Data Report:Submit the data and test report which is reviewed by the quality and technical management along with the summary report of the turkey solution.

Contract review:The contract will be reviewed according to requirement of the market or client, based on actual situation and BE R&D or BE customized development against product, and in aspect of resources allocation (personnel arrangement and material preparation) required to fulfill the task on schedule.

Project Established:To start from helping client with solving problems and difficulties, customized the turkey solution, including but not limit to testing, auditing and training, and etc..

Development of Methodology:Exploration and establish of the Methodology.

Method Validation:Taking account of clinic trails, Methodological program will be validated according to related requirement of validation content and acceptance criteria in FDA, CFDA and Chinese Pharmacopoeia.

QA Audit:QA will offer quality assurance for method validation and audit all data generated.

Determination of Sample Analysis Method:Taking account of clinic trails, and based on validated methodology proposal, sample analysis proposal will be made.

Sample Test and Analysis:Sample will be tested and analyzed according to established analysis method.

QA Audit:QA will offer quality assurance for sample analysis and audit all data generated.

Data Submit and Report Proposing:Submit the data audited by QA and propose the final sample analysis report.

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