NABL - Location Kochi accredited as per ISO/IEC 17025: 2017, vide certificate No. TC-6338                                                                 AGMARK - QUALITY CERTIFICATION MARK FOR AGRICULTURAL PRODUCTS.                                                                 APEDA - AGRICULTURAL & PROCESSED FOOD EXPORT DEVELOPMENT AUTHORITY                                                                 POLLUTION CONTROL BOARD                                                                 EIC - EXPORT INSPECTION COUNCIL, GOVT. OF INDIA                                                                 DRUGS CONTROL DEPARTMENT - KERALA                                                                 TEA BOARD OF INDIA                                                                 FSSAI - FOOD SAFETY STANDARD AUTHORITY OF INDIA                                                                  BIS - BUREAU OF INDIAN STANDARDS                                                              

About us

INTERFIELD LABORATORIES is an independent testing laboratory, established in 1995 for the organoleptic and microbiological testing of marine products.  Subsequently the facilities of the laboratory were enhanced to include chemical analysis and biological analysis, anticipating the potential in other industries like spices, cashew kernels, and various other agricultural products.  Since 2000, the laboratory has been accepting samples other than marine products.

INTERFIELD LABORATORIES has a facility of about 11000 sq.ft.

Legal identity: The laboratory is approved by the Export Inspection Council of India, Agricultural Produce Export Development Authority, Food safety & Standards Authority of India, Kerala State Pollution Control Board as ‘A’ grade laboratory and approved by the Drugs Controller of India to analyse the drugs and pharmaceutical products.

Quality Policy

Team Interfield Laboratories shall build and continuously improve this laboratory to create a center of excellence in Biological and Chemical analysis.  The management at every level shall be transparent and will maintain the highest ethical standards to create an environment conducive for continual improvement and at all times ensure compliance with IS:ISO /IEC 17025:2017

 We achieve this goal through                                            

  • Establishing and implementing a well defined and documented management  system
  • Adopting internationally recognized  test procedures
  • Installation of appropriate state-of-the-art equipments
  • Imparting systematic training to staff
  • Uncompromising quality checks
  • Maintaining  cordial relationship with Customers
  • Continual up- gradation of the management system based on customer feedback.
  • Quick, fair and ethical response to customer complaints.
  • Familiarizing all the testing personnel with the quality documentation and implement the policies and procedures of the quality system based on ISO IEC 17025: 2017 in their work and ensuring compliance to the standard.

Quality Assurance

  The Quality assurance includes demonstrating the following:

  • having trained, competent and knowledgeable personnel
  • having suitable laboratory facilities
  • using validated methods providing estimates of the measurement uncertainty
  • demonstrating traceability of measurement by using calibrated instruments and equipment and certified reference materials
  • demonstrating sample traceability by logging, labelling, storing and tracking samples appropriately
  • monitoring performance with QC standards, control charts, replicate samples and proficiency testing.

Interfield Laboratories has a dynamic and ongoing process of quality assurance which encompasses all the three phases of laboratory activities, ie preanalytical, analytical and postanalytical.

Preanalytical includes the availability of trained personnel, sampling based on statistical methods wherever required, verification of condition of sample at the time of receipt, proper storage of sample till analysis in order to  protect the integrity of the sample till it is taken for analysis, delivery of the sample in the lab for analysis, giving a unique identification to each sample so that the samples can always be traced with ease etc.

Analytical phase includes the use of standard method or a validated method, calibration of instrument and reaffirming the confidence in the calibration as per laid down schedule, use of valid reference material, internal standards, quality control samples and use of quality reagents.

Post-analytical phase encompasses interpreting and verifying results, reporting the results with all the necessary details and reviewing the QC.