FindTestingLabs
Registers refreshed 2026-10-18.See refresh dates
United Kingdom

Total Clean Air

Units 1-4, Gravenchon Way, Street Business Park, Street, BA16 0HS, Somerset, United Kingdom

UKAS|27642ISO/IEC 17025Register refreshed 2026-10-09
Certificates
1
Scope items
2
Standards
6
Locations
1

Free. We check which accredited labs can do it, starting with this one, and reply within two working days with who can do it, how fast, and roughly what it costs.

Only the laboratory you pick gets your contact details. We ask the others without them.

Follow this lab

We will email you if this laboratory’s accreditation status or scope changes. No newsletter, only changes.

Work at Total Clean Air?

Claim this profile to keep it accurate.

Register record

UKASRefreshed
27642Active

Accredited standards

6

Our reading of the UKAS scope: each standard once, with its official name where we have checked it. Click a standard to see the scope line it comes from, word for word.

EN 14175-3Name not checked yet
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

EN 14175-4Name not checked yet
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

ISO 14644-1Cleanrooms and associated controlled environments - Part 1: Classification of air cleanliness by particle concentration
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

ISO 14644-2Cleanrooms and associated controlled environments - Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

ISO 14644-3Cleanrooms and associated controlled environments - Part 3: Test methods
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

ISO 14644-4Cleanrooms and associated controlled environments - Part 4: Design, construction and start-up
As written on the certificate · Line 2 (UKAS 27642)

BS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025

Scope as published by UKAS

2 lines
UKAS

ISO/IEC 17025

Active

27642

View scope

Accredited scope, certificate 27642

LineDisciplineMethodMatrixRange
1-ISO/IEC 17025:2017Ambient air-
2Biological TestingBS EN ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; BS 7989; ISO/IEC 17025:2017 Schedule of Accreditation issued by United Kingdom Accreditation Service 2; ISO 14644-1:2015 BS EN ISO 14644-2:2015 BS EN ISO 14644-3:2019 BS EN ISO 14644-4:2022 BS EN 14175-3:2019 BS EN 14175-4:2004 BS 7989:2001 EU EudraLex Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use: Annex 1: Manufacture of Sterile Medicinal Products 2022 HSG258; IEC 17025Ambient air0.25 to 25 m/s

Ranges are reproduced from the accredited scope document as published, and only where we found that range printed in the document for the line. Otherwise the cell reads “See scope document”. An absent range means the register did not state one. Line numbers are ours, for cross-reference; they follow the order of the scope document.

Location

Units 1-4, Gravenchon Way, Street Business Park, Street, Somerset, BA16 0HS, GB

51.16175, -3.07539

Open in Maps

Accreditation data refreshed from the UKAS register on .

This page mirrors a public register. For a purchasing, audit or regulatory decision, confirm against the UKAS entry linked above.