
Report Recall notification Letter
Report Recall notification Letter Mistake proof working environment is best examples for quality management system, technically in case of non conformance found during the internal activities by quality control department due to used methods, standards or work instruction reference as…

Job responsibility & Authority formats
Job responsibility & Authority formats When the management appoints any person or change duties that Human Resource department / Personal Department being active to reflects are capture in line with management assigned duties to any person, Human resource department…

Action Status on management review meeting
Action Status on management review meeting MRM (Management Review meeting) is command review on previous activity happen during the period defined for management review meeting, like frequency of the management review meeting is quarterly or six month that all…

Test Report for Laboratory
Test Report for Laboratory The result of tested each sample, calibrations by laboratory written accurate, clearly & focus on objective or tests according to standards, specifications instructions & method is test report. Testing report should be cover the all the…

Non standard method test format for laboratory
Non standard method test format for laboratory Laboratories are follows some international standards that almost acceptable methods & validate testing if done by laboratory, if the laboratory follow the standard that customers are believe or acceptable for application’s requirements….

Authorized Signatory
Authorized Signatory : List of qualified Personnel for Authorized Signatory As per international standards ISO 17025 technical requirements as well laboratory internal requirements that each signature has its own requirements, in the laboratory requirements are signatory is important part…

capa audit checklist
CAPA ( CORRECTIVE ACTION PREVENTIVE ACTION ) AUDIT CHECKLIST Is a documented procedure for Corrective Actions preventive action available? Is a Corrective action & preventive action prepared for any non conformity detected? Is the Corrective action reviewed to find…

ISO 17025 – General Checklist
ISO 17025 – General Checklist Are all calibration and measurements are traceable? Traceable flow are available? verified & Controlled? Concern Peoples are aware of calibration & measurement tractability? are inter laboratory comparisons made to establish calibration? Is there a procedure…

equipment checklist – iso 17025 clause no 5.5
Equipment checklist – ISO 17025 clause no 5.5 Is the laboratory adequately equipped? Are all the equipment is calibrated and calibration status are documented, recorded & controlled? Equipment unique number is displayed on the equipment? and same will be…
