Certificate of Good Manufacturing Practices (GMP) Compliance

Natural Health Product (NHP) Site Licence (#302531)

ISO 9001:2015, ISO 14001:2015 and ISO 45001:2018 registration

FDA Establishment Registration for analysis, manufacturing, packaging and labelling of OTC drug products under a monograph in the USA 

Affiliate Biosafety Level 2 (BSL2) Toxins and Pathogen Site License (LA-20-0003765)

Dedicated regulatory compliance group with separate and distinct Quality Assurance (QA) and Quality Control (QC) departments

MasterControl™ EQMS, dicentra™ GMP training, KGK Science Pharmacovigilance support and statistical sampling – ANSI

8,000 sq.ft. GMP separate clean room production space

20,000 sq.ft. GMP climate monitored and controlled warehouse area

10,000+ sq.ft. of QA/QC, R&D and full laboratory services

State-of-the-art negative and positive pressure clean rooms built to ISO 8 specifications (flammables compliant)

Closed-loop distribution clean room

Dedicated sampling and dispensing rooms

In-house packaging manufacturing capacity with sustainable options

Unique, customizable packaging equipment

High-capacity packaging and labelling equipment