Asgard

Quality Guarantees

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Quality, Health & Safety
& the Environment

At Asgard, our entire team understands the need for cGMP (GxP) compliance and always adhere to the highest regulated standards set out by the various regional and regulatory bodies, such as ISO and the FDA. Our success is strengthened by our total commitment to quality, health and safety and the environment. Asgard Cleanroom Solutions are accredited under I.S. EN ISO 9001:2015 (Quality) and ISO 45001:2018 (Health & Safety).

Our Gaurantees

All BioPharmaceutical environments are specified, designed and built by Asgard Cleanroom Solutions are in accordance to the following:
  • ISO 14644

Classification of air cleanliness by particle concentration.

  • Biosafety

In Microbiological and Biomedical Laboratories, 5th Edition, 2007.

  • EU EudraLex

Volume 4 EU GMP
(Medicinal Products for Human & Veterinary Use).

  • 21 Code of Federal Regulations Part 210

Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs.

  • EN10326-1:2016

For mechanical vibration within Laboratories.

  • ISPE

Good Engineering Practice & Maintenance and FDA requirements Products and installation with all qualifications (FAT / SAT / IQ / OQ).

  • ASTM Standard E2500, 2007

(Standard Guide for Specification, Design, and Verification of Pharmaceutical & Biopharmaceutical Manufacturing Systems and Equipment).

Our Accreditations

Asgard Cleanroom Solutions continuously show commitment to health and safety standards by having ConstuctionLine Gold Membership status, achieving the Acclaim Accreditation certificate for 2021, SSIP & PAS91 Contractor Accreditation certificates, a certificate of accreditation with Building Confidence powered by Achilles and most recently our CHAS Premium Accreditation.