From raw materials to finished products, we connect you with accredited
laboratories across North America for all your analytical testing needs.
Raw materials, bulk, and finished products
Safety and efficacy testing
Cannabinoid profiling and compliance
Microbial limit and sterility testing
ICH-compliant stability programs
Comprehensive testing capabilities using state-of-the-art instrumentation and validated
methods.
FTIR
UV-Vis spectroscopy
HPLC
TLC
HPCL
GC
UV-Vis
FT-IR
Titration
HPCL
GC
LC-MS/MS
HPCL
ICP-OES
AAS
USP Apparatus I
USP Apparatus II
GC-FID
GC-MS
GC-MS
pH
Viscosity
Moisture
Hardness
Friability
X-ray Diffraction
Differential Scanning CalorimetryMS
Chiral HPLC
LC-MS/MS
GC-MS/MS
Complete microbial quality control testing following USP <61>/<62> and other pharmacopoeial methods.
Comprehensive stability testing programs designed per ICH Q1A(R2) guidelines to
support your product registration.
25°C ± 2°C / 65% RH ± 5%
Up to 36 months
40°C ± 2°C / 75% RH ± 5%
6 months
30°C ± 2°C / 65% RH ± 5%
6 months
2–4°C
Up to 24 months
ICH Q1B Guidelines
As per protocol
Multiple cycles
As per protocol
Our expert team provides comprehensive analytical R&D support including method
development, validation, verification, and transfer.
Contact us today for a free consultation and competitive quote.
Your trusted partner for analytical testing services and reference standards acrossNorth America.