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Quality Policy And Conditions

MUDRA DIAGNOSTICS maintains the highest standards of quality control in all aspects of laboratory work. Our laboratory's Quality Management System ensures adherence

  • To the principles of all accreditations, including NABL – ISO 15189:2012 (National Accreditation Board for Testing and Calibration Laboratories) for each test within the scope of accreditation and beyond.
  • We timely update and fully validate test methods, processes, and control mechanisms to guarantee the accuracy and reliability of our test results.
quality

The revised objectives of our Quality Control system are as follows:

  • Implement Bar-Coded operations to ensure complete traceability throughout the sample flow process, guaranteeing accurate tracking and monitoring of samples.
  • Enhance sample handling procedures and manage environmental conditions meticulously to minimize any potential impact on the results and maintain high-quality outcomes.
  • To continually improve the practices of our clients, franchise partners, associate doctors, clinics, and hospitals, we’ll proactively monitor their training needs, identify gaps in processes, and guide them to provide the best patient care. We’ll ensure accurate and clear reporting of results and conduct root cause analysis for any deviations from protocols.
  • solutions to the specified reasons.

Ensures  a continual enhancement of, performance, and supervision of the quality procedure and aspires to advancement  in the persuasiveness of the

  • We implement a robust quality system, overseen by experts, to ensure that our services consistently meet and exceed expectations. Regular intervals of assessment help us maintain high standards in turn-around time, sample collection hygiene, and the reliability of our services.
  • Ensure that each test is performed by qualified and trained staff, and offer opportunities for them to enhance their knowledge and skills. This will help maintain high-quality standards and foster professional development among the staff.
  • To improve both personal and organizational growth, prioritize using top-notch equipment that is well-maintained and calibrated. Whenever feasible, ensure measurements are traceable to recognized standards. Also, consider optimizing and updating all content accordingly.
  • To improve equipment performance, it’s crucial to adhere to recognized standards and explore cutting-edge methods. Implementing technology upgrades can enhance accuracy and simplify processes, leading to better results. When modifying content, ensure it aligns with the latest advancements and best practices in the field.
  • Utilize internal audits and different assessments to assure the quality procedure complies with prerequisites; assure difficulties are analyzed.
  • Immediately, the fundamental reason(s) were identified, and efficient measures were implemented to avert repetition. Establish a seamless communication system to ensure data is swiftly accessible to those who require it, both within the organization and externally.

Supporting external partners in delivering quality services is a crucial aspect of our organization. We closely monitor and assist our franchise and service partners to ensure they remain sensitive to all aspects of service delivery, while also maintaining consistent quality standards.

Condition of Reporting

  1. It is supposed that the sample accompanying their  TRF (Test Requisition Form where the fragments of the patients are documented) is of the same patient whose attributes are there any in the TRF.
2. A test required might have not been conducted due to the following justifications:
  • 2.1 Insufficient portion of the sample required to perform the test.
  • 2.2 Poor quality of the Specimen not conference the quality standards
  • (hemolysis of specimen/clotted.)
  • 2.3 Incorrect sample classification as directed to perform a test.
  1. Test(s) may be partially or entirely dispensed with due to incorrect test principle, incorrect name of their test, or incorrect type of other sample. A contract shall be created and it is predicted that a renewed specimen

will be dispatched to a laboratory for estimation of the identical parameters (s).

  1. The effects of laboratory research are dependent on the quality of the sample as well as the assay methods/technologies to be used. All specimens accumulated for trials are needed to be formulated, accumulated, marked, and brought up to the processing laboratory as per the prescribed policies of MUDRA DIAGNOSTICS.
  2. MUDRA DIAGNOSTICS. the laboratory cannot be held responsible for inaccurate outcomes of a specimen that changed course from the cases published.
  3. There can be several times aspects like a sample’s unconsenting orientation to warm or transit throughout uneven terrain which affects the quality of test outcomes. Accordingly, a 2% chance of misconception/ digression in consequences is a probability.
  4. For particular classifications of tests, the statement may be carrying a “PRELIMINARY ” level signifying that outcomes are yet to be ascertained for one (or more) tests. For instance, in the possibility of specific microbiology tests, a “FINAL” culture, identification, or medication defenselessness effect might have been pending. In such circumstances, the status “RESULT PENDING” will be touched on in the statement. The exact date shall take the place of the examination outcomes whenever prepared.
  5. If their collection date or any other elements was not declared in the Test Petition Form, the identical will not be published on the report. In cases where the missing assignment information is mandatory for statement generation or conference accreditation policies, the sample shall not be processed ll. Test parameters exuded from the “scope” of NABL accreditation shall be commemorated by asterisks.
  6. In issue you are not the conscious recipients of the report, please immediately inform the issuing entity. Any use, exposure, copy, or allotment of any scope of such report, is illegal and rigidly restricted.
  7. Few examinations may be directed to other laboratories to furnish broader test menus to the patients. The elements of the laboratory where the specimen existed are directed and can be acquired from the Customer.
  8. Care department. Statements describing the relation the effects against the different laboratories shall be skimmed into simply if it lived the precise sample that existed partition and sent it in the similar situations to all laboratories and processed.

12 on the same technology.