E&O Labs

E&O Labs

E&O Laboratories

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E&O Laboratories Ltd’s head office is based in Central Scotland with two fully automated manufacturing facilities and two licenced donor animal blood harvesting farms. All operational functions adhere to the required industry compliance criteria.
E&O Laboratories Ltd is certified to ISO 9001:2015 & ISO 13485:2016 for “The development, manufacture and supply of ready-to-use culture media, dehydrated culture media, blood products, microbiological supplements/reagents and microbiological analytical services. ”
Quality control methods are accredited by UKAS to EN ISO/IEC 17025:2017.
E&O Laboratories manufacture a comprehensive range of Ready-To-Use Culture Media in various formats along with Dehydrated Culture Media, Antibiotic Supplement/Reagents, donor animal Blood and Serum, all available in a wide range of volumes and containers.
Clinical Veterinary Aquaculture Pharmaceutical Industrial Cosmetic Food, Water & Environmental
E&O Laboratories Ltd is the UK’s largest, and leading, privately owned, manufacturer of Culture Media. E&O supply a comprehensive, high quality product range in various formats and in a wide range of volumes and containers to satisfy all the different business sector’s compliance criteria and laboratory requirements.
E&O have two cGMP manufacturing sites to facilitate their fully automated production lines, steam sterilisation areas, validated clean-rooms and associated warehouse logistics function. Customer service, technical support, R&D, QC and QA are all sited at the main office in the Burnhouse facility.
All clinical products are CE marked, with industrial products being compliant with the Harmonized (USP/EP/JP) Pharmacopoeia standards.
Both sites are certified to ISO 9001:2015 & ISO 13485:2016 with quality control accredited by UKAS to EN ISO/IEC 17025:2017.
Pre-poured plates Bottled media Bagged media Tubes/Vials/Jars
E&O manufacture a wide range of formulations in controlled and validated production facilities equipped with the most modern automated equipment. Following an accurately controlled and documented formulation protocol, a defined weight of raw materials is added to a measured fluid prior to sterilisation/filtration/pasteurisation or inspissation.
Production batches range from 2 – 400litre and are transferred via colour coded sterilised tubing for automated dispensing into petri-dishes, bottles, tubes, vials or bags of varying sizes and volumes depending on client requirements. Dispensing, ink-jetting and final packaging are all performed in environmentally controlled clean-room defined areas validated to: ISO 14644-1 (Class7), EU GMP (Grade C).
General Purpose Media Differential Media Selective Media Enrichment Media
E&O’s powder department pride themselves on their raw material selection process of complex nutritional components from around the globe. Following extensive testing criteria, batch reservation is contracted on an annual basis. Milling and blending using controlled and validated formulations and SOP’s guarantee batch to batch consistency of performance. All processes are housed in a controlled environment to ensure minimum degradation from moisture, heat and lighting effects.
Finished product is available in pre-weighed 500gm – 50kg containers/bags to suit customer requirements.
E&O offer a wide range of complementary antibiotic supplements and reagents for the selectivity, enrichment and chemical differentiation of media. They are manufactured in formats to suit varying requirements and batch volumes of different industry sectors. Packed in powder sachets, lyophilised vials, deep frozen bottles and tablet formats for 500ml – 100lt batch production.
Donor Horse Blood Donor Sheep Blood Filtered Serum Lyophilised Plasma
E&O Laboratories have been harvesting donor animal blood since 1978 on their two dedicated farm units. Careful animal selection, strict quarantine procedures and rigorous veterinary inspections ensures high quality donor blood products. Validated seasonal feeding regimes and high quality stock management guarantees consistent shelf-life with minimal red cell fragility and a defined Pack Cell Volume.
All donor collection procedures are carried out under a Project Licence from the Home Office under the Animals (Scientific procedures) Act 1986.
Defibrinated donor harvested blood is transferred from the farm unit to the laboratory where it is pooled into varying batch sizes, depending on customer requirements, before being dispensed into sterile bottles or bags. All blood products are routinely quality controlled within our UKAS accredited laboratory before being released for shipping.
Donor Horse Serum is separated from the red cells aseptically and then filtered through a series of filters before being pooled into a 300 litre batch and then, through a final 0. 2µm sterile filter prior to bottling and deep freezing.
E&O Laboratories

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  • Worldwide locations
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E&O Laboratories

E&O Laboratories Ltd’s head office is based in Central Scotland with two fully automated manufacturing facilities and two licenced donor animal blood harvesting farms. All operational functions adhere to the required industry compliance criteria.
E&O Laboratories Ltd is certified to ISO 9001:2015 & ISO 13485:2016 for “The development, manufacture and supply of ready-to-use culture media, dehydrated culture media, blood products, microbiological supplements/reagents and microbiological analytical services. ”
Quality control methods are accredited by UKAS to EN ISO/IEC 17025:2017.
E&O Laboratories manufacture a comprehensive range of Ready-To-Use Culture Media in various formats along with Dehydrated Culture Media, Antibiotic Supplement/Reagents, donor animal Blood and Serum, all available in a wide range of volumes and containers.
Clinical Veterinary Aquaculture Pharmaceutical Industrial Cosmetic Food, Water & Environmental
E&O Laboratories Ltd is the UK’s largest, and leading, privately owned, manufacturer of Culture Media. E&O supply a comprehensive, high quality product range in various formats and in a wide range of volumes and containers to satisfy all the different business sector’s compliance criteria and laboratory requirements.
E&O have two cGMP manufacturing sites to facilitate their fully automated production lines, steam sterilisation areas, validated clean-rooms and associated warehouse logistics function. Customer service, technical support, R&D, QC and QA are all sited at the main office in the Burnhouse facility.
All clinical products are CE marked, with industrial products being compliant with the Harmonized (USP/EP/JP) Pharmacopoeia standards.
Both sites are certified to ISO 9001:2015 & ISO 13485:2016 with quality control accredited by UKAS to EN ISO/IEC 17025:2017.
Pre-poured plates Bottled media Bagged media Tubes/Vials/Jars
E&O manufacture a wide range of formulations in controlled and validated production facilities equipped with the most modern automated equipment. Following an accurately controlled and documented formulation protocol, a defined weight of raw materials is added to a measured fluid prior to sterilisation/filtration/pasteurisation or inspissation.
Production batches range from 2 – 400litre and are transferred via colour coded sterilised tubing for automated dispensing into petri-dishes, bottles, tubes, vials or bags of varying sizes and volumes depending on client requirements. Dispensing, ink-jetting and final packaging are all performed in environmentally controlled clean-room defined areas validated to: ISO 14644-1 (Class7), EU GMP (Grade C).
General Purpose Media Differential Media Selective Media Enrichment Media
E&O’s powder department pride themselves on their raw material selection process of complex nutritional components from around the globe. Following extensive testing criteria, batch reservation is contracted on an annual basis. Milling and blending using controlled and validated formulations and SOP’s guarantee batch to batch consistency of performance. All processes are housed in a controlled environment to ensure minimum degradation from moisture, heat and lighting effects.
Finished product is available in pre-weighed 500gm – 50kg containers/bags to suit customer requirements.
E&O offer a wide range of complementary antibiotic supplements and reagents for the selectivity, enrichment and chemical differentiation of media. They are manufactured in formats to suit varying requirements and batch volumes of different industry sectors. Packed in powder sachets, lyophilised vials, deep frozen bottles and tablet formats for 500ml – 100lt batch production.
Donor Horse Blood Donor Sheep Blood Filtered Serum Lyophilised Plasma
E&O Laboratories have been harvesting donor animal blood since 1978 on their two dedicated farm units. Careful animal selection, strict quarantine procedures and rigorous veterinary inspections ensures high quality donor blood products. Validated seasonal feeding regimes and high quality stock management guarantees consistent shelf-life with minimal red cell fragility and a defined Pack Cell Volume.
All donor collection procedures are carried out under a Project Licence from the Home Office under the Animals (Scientific procedures) Act 1986.
Defibrinated donor harvested blood is transferred from the farm unit to the laboratory where it is pooled into varying batch sizes, depending on customer requirements, before being dispensed into sterile bottles or bags. All blood products are routinely quality controlled within our UKAS accredited laboratory before being released for shipping.
Donor Horse Serum is separated from the red cells aseptically and then filtered through a series of filters before being pooled into a 300 litre batch and then, through a final 0. 2µm sterile filter prior to bottling and deep freezing.
E&O Laboratories Ltd - rapidmicrobiology

E&O Laboratories Ltd – rapidmicrobiology

E&O Laboratories Ltd
E&O is a privately owned company which has been supplying the UK’s NHS as well as several European and Middle Eastern distributors with high quality sterile blood products for the last 30 years. In 1995 the company diversified its core business into the manufacture of ready-to-use microbiological culture media. Primarily the focus was on the clinical sector and then latterly the business has grown to incorporate all food, water, veterinary, pharmaceutical, industrial and cosmetic laboratories’ media requirements.

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