Compliance
Company compliance ensures all manufacturing processes and services meet the required Environmental, Health and Safety and Quality Standards regulated within the different industry sectors using Microbiological Culture Media both nationally and internationally.
Compliance
Quality Assurance
Quality underpins every part of E&O’s manufacturing and service operations. All processes are designed and controlled to meet the highest Environmental, Health & Safety and Quality standards required across the microbiological culture media industry.
E&O Laboratories Ltd is certified to ISO 9001:2015 & BS EN ISO 13485:2016 for “The development, manufacture and supply of microbiological prepared culture media, dehydrated culture media, blood products, microbiological supplements/reagents and microbiological analytical services”
The Quality management system is designed and written to ensure accuracy and traceability throughout the business.
All manufactured Culture Media & raw material testing is subcontracted to Quality Control Department for quality control.
Test methods are accredited by UKAS in compliance with BS EN ISO/IEC 17025:2017. Methodology is based on ISO 11133:2014.
E&O Laboratories Ltd’s farm division holds a Home Office Project License for the Animals (Scientific Procedures) Act 1986 to routinely harvest & process donor animal blood products.
All Animal technicians hold personal licenses and two farms are licensed designated areas.
E&O Laboratories Ltd are an MHRA registered supplier and provide an extensive range of clinical reagents which are CE marked in compliance with the European In-Vitro Diagnostics Medical Devices Regulation 98/79/EC.
Pharmaceutical culture media manufacture comply with the Harmonized MTL methods in the US/EU/JP Pharmacopoeias – International Standards and ISO criteria.
E&O Laboratories Management System incorporates the relevant criteria of Good Manufacturing Practice (cGMP) and Good Laboratory Practice (cGLP) to ensure products are consistently manufactured and controlled to defined quality.
Quality Assurance
Quality underpins every part of E&O’s manufacturing and service operations. All processes are designed and controlled to meet the highest Environmental, Health & Safety and Quality standards required across the microbiological culture media industry.
E&O Laboratories Ltd is certified to ISO 9001:2015 & BS EN ISO 13485:2016 for “The development, manufacture and supply of microbiological prepared culture media, dehydrated culture media, blood products, microbiological supplements/reagents and microbiological analytical services”
The Quality management system is designed and written to ensure accuracy and traceability throughout the business.
All manufactured Culture Media & raw material testing is subcontracted to Quality Control Department for quality control.
Test methods are accredited by UKAS in compliance with BS EN ISO/IEC 17025:2017. Methodology is based on ISO 11133:2014.
E&O Laboratories Ltd’s farm division holds a Home Office Project License for the Animals (Scientific Procedures) Act 1986 to routinely harvest & process donor animal blood products.
All Animal technicians hold personal licenses and two farms are licensed designated areas.
E&O Laboratories Ltd are an MHRA registered supplier and provide an extensive range of clinical reagents which are CE marked in compliance with the European In-Vitro Diagnostics Medical Devices Regulation 98/79/EC.
Pharmaceutical culture media manufacture comply with the Harmonized MTL methods in the US/EU/JP Pharmacopoeias – International Standards and ISO criteria.
E&O Laboratories Management System incorporates the relevant criteria of Good Manufacturing Practice (cGMP) and Good Laboratory Practice (cGLP) to ensure products are consistently manufactured and controlled to defined quality.
Research & Development
E&O Laboratories employ a highly qualified team of scientists to formulate new media, improve on existing formulations and work with clients to design specialised diluents/reagents and new culture media.
A dedicated laboratory area with calibrated modern equipment allows a wide variety of media assays to be performed and designed before scaling up for final customer verification.
E&O can source raw materials worldwide and has the in-house expertise to mill, blend, sterilise, aliquot and quality control to any specification in volumes/weights and containers to satisfy clients individual requirements.
Research & Development
E&O Laboratories employ a very highly qualified team of scientists to formulate new media, improve on existing formulations and work with clients to design specialised diluents/reagents and new culture media.
E&O can source raw materials worldwide and has the in-house expertise to mill, blend, sterilise, aliquot and quality control to any specification in volumes/weights and containers to satisfy clients individual requirements.
Quality Control
Quality underpins every part of E&O’s manufacturing and service operations. All processes are designed and controlled to meet the highest Environmental, Health & Safety and Quality standards required across the microbiological culture media industry.
Quality Control Department carries out quality control testing on the manufactured ready-to-use microbiological culture media, donor animal blood & sera and the antibiotic supplements/reagents.
See Our Range
Quality Control Department is responsible for the reporting of all the results from the rigorous testing and monitoring regime of E&O Laboratories controlled environment areas regarding air supply, DI water and general cGMP/cGLP hygiene for the manufacturing areas in their facilities at Burnhouse and Westfield.
See Our Range
E&O Laboratories Ltd's technical team are continually striving to improve product performance through selective raw material sourcing, sensitive & accurate media sterilisation, innovative packaging/storage solutions and continual ongoing shelf-life analysis.
See Our Range
Quality control certification is available on-line for all production batch manufacture following the completion of the QC protocol and all specifications are met and the batch is formally released for stock.
See Our Range
Quality Control
Quality underpins every part of E&O’s manufacturing and service operations. All processes are designed and controlled to meet the highest Environmental, Health & Safety and Quality standards required across the microbiological culture media industry.
Quality Control Department carries out quality control testing on the manufactured ready-to-use microbiological culture media, donor animal blood & sera and the antibiotic supplements/reagents.
See Our Range
Quality Control Department is responsible for the reporting of all the results from the rigorous testing and monitoring regime of E&O Laboratories controlled environment areas regarding air supply, DI water and general cGMP/cGLP hygiene for the manufacturing areas in their facilities at Burnhouse and Westfield.
See Our Range
E&O Laboratories Ltd's technical team are continually striving to improve product performance through selective raw material sourcing, sensitive & accurate media sterilisation, innovative packaging/storage solutions and continual ongoing shelf-life analysis.
See Our Range
Quality control certification is available on-line for all production batch manufacture following the completion of the QC protocol and all specifications are met and the batch is formally released for stock.
See Our Range