Non conforming product Register
Non conforming product Register Non conforming product meaning is product that manufactured is not meet requirements of product criteria, supplier specific requirement or standard requirement of product. During the manufacturing process product when any mistake, leak of standard procedures…
Supplier Audit Checklist
Supplier Audit Checklist International Standards ISO 9001 gives the guideline to improve quality in working environment as well as quality product to enhance customer satisfactions. ISO 9001 that is quality management system, probably focus on quality management to improve…
Shift wise duty chart
Shift wise duty chart Man power management is very big challenge for the human resource department when nos of employee amount are huge and than also very complicated to manage all the employees as shift wise with effective manpower management…
Internal Rejection format
Internal Rejection format Internal rejection Format is used for the monitoring and controls to reject material during manufacturing various processes, same will be enabling to monitor & calculate reworks and scrape for the particular customer and against order no. Internal…
Re-order level for critical spares parts
Re-order level for critical spares parts Storage department are always find the solutions to maintain stock to being level against user department requirements, for the store department various techniques are used for the maintain stocks, its is very critical incase…
Operational manual /Literature of Equipment
Operational manual /Literature of Equipment List Operational manual / Literature are guideline & instructions to operate the equipments & information of safety & precautions. Operating manual / literature of equipment are comes along with equipment when we buy new. All…
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…
Complaint register for laboratory
Complaint register for laboratory Laboratory is not a industrial type other unit that complains from customers having a huge parameters and other minor and major problems that are customer can understand reason is the all the works and on huge…
Equipment maintenance record
Equipment maintenance record At any location of laboratory having a trouble in equipment / instruments, failed maintenance department / owner of equipment are fill this format for the record to enable further analysis of damage of equipment. This format…