The foundation of Dvine Laboratories is based on our commitment to quality at all levels of the organization. Since inception our company has continually strived for improvements at all levels of the manufacturing process.
Before our industry was federally regulated Dvine Laboratories voluntarily regulated our process based on Quality Management and Good Manufacturing Process’s. Additionally adding a dedicated laboratory equipped with Gas Chromatography to test all aspects of our Raw Materials.
Dvine Laboratories was the First Lab in Canada to achieve and maintain today the following Certifications:
- ISO 9001 Quality Management
- ISO 22716 Cosmetic cGMP
- ISO 17025 Accredited Lab Testing Facility
By maintaining these critical standards our customers can rest knowing that every aspect of our manufacturing processes are Tested, Verified and Traced from the time a raw material enters the building to when the final package is assembled and shipped.
Our facility is also fully automated with Manufacturing Resource Planning Software (MRP) powered by Mysis Manufacturing. Mysis ensures we always have the materials we require in inventory while also tracking every component used in any customer order, rolling this up to a master Lot and Batch ID, where if there was ever an issue we can trace back to each Raw component to identify the failure in the quality of a product.
Additional consideration is also applied to ongoing Batch Sampling where every day our Quality Control team select various finished goods to test in the Lab for correct Nicotine Concentrations, Proper Ratio of PG/VG and screening for any known harmful components that should not be in any e-liquid products. All Raw materials are previously tested and screened before production use, however this is a second step process is to ensure the quality of the ingredients.
We are very proud and confident in the Quality platforms we have built and operate and should you like more information we would be happy to schedule a tour or call with you.