QC Certificate Requests
Use the tool below to retrieve historical quality control certification for product batches.
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Quality Certificate Lookup
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Supporting Quality & Compliance
Every batch of E&O culture media is manufactured and quality controlled in accordance with our validated procedures before release. Our online certificate lookup provides quick access to historical Quality Control Certificates, helping laboratories maintain complete documentation for audit, accreditation and regulatory compliance.
Compliance
Quality Assurance
Quality underpins every part of E&O’s manufacturing and service operations. All processes are designed and controlled to meet the required standards across all the microbiological culture media industry sectors.
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.