All the ingredients that we used are tested and certified as pharmaceutical grade. All the flavours we use have been rigorously screened for any known respiratory sensitisers by a team of qualified and accredited toxicologists.
We apply pharmaceutical practices to the mixing and bottling of our e-liquids, including supporting functions such as contamination control, record keeping, training, maintenance, cleaning and cleanliness, etc. For every batch produced, we record and store all relevant data relating to its storage, handling, manufacture and testing prior to release by our Quality Control team.
With a facility which has held a MHRA licence for over 25 years, and a longstanding and committed workforce highly trained in Pharmaceutical manufacturing practices, accompanied with years of experience in e-liquid manufacturing, we guarantee consistency, quality, safety and control when manufacturing our products.
We know the importance of Product Quality, and therefore we commissioned on-site a specialised custom-built laboratory, staffed with analysts who are highly experienced in testing pharmaceuticals, e-liquids and e-liquid vapours.
We meticulously test all raw ingredients as well as every batch of finished product for all Critical Quality Attributes at a standard far higher than required by TPD.
Our experience, quality disciplines and accreditations are unrivalled in the e-liquid market. We volunteer to be regularly inspected by internationally renowned Quality Certification bodies, and our external accreditations speak for themselves:
✓ The manufacturing site has held an MHRA European GMP Licence for 25 years for the handling and assembly of medicinal products
✓ BSI GMP (Good Manufacturing Practices)
✓ BSI HACCP (Hazardous Analysis & Critical Control Point)
✓ ISO 9001:2015 Quality Management System accreditation
✓ ISO 13485:2016 Medical Device accreditation
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