Services provided

Expertise in Pharmaceutical/Cosmetic/OTC/NHP and raw material analysis according to USP, BP, EP, JP, FCC and in-house methods.
Quality control (QC).
Product stability studies according to ICH guideline Q1A(R2).
Development, validation, transfer and qualification of analytical methods according to FDA guideline: Satbility-Indicating Assay, Impurities/Degradation products, Residual solvents, Dissolution, Aflatoxins, Packaging, etc.
Turnkey solution
On special agreement, we can develop an analysis method or improve an existing method.

Licences:

Laboval is accredited by:

Health Canada Controlled Substances Licence and Establishment Licence

Licence of Food and Drug Administration (FDA)

License for Cannabis Testing

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Version 2.6 of OpenLab CDS from Agilent
UPLC detector DAD
HPLC detectors: DAD, ELSD, RID, UV
GC detector FID (direct injection and headspace)
GC-MS
ICP-MS
UV
FTIR
Lovibond
AA
SPE SYSTEM
Temperature controlled centrifuge
Dissolution baths
Karl Fisher
Microbalances
Wet Chemistry
Thin-layer chromatography testing (TLC)
Titration Assays
Aflatoxins
Full range of stability testing and storage services under ICH conditions: 25°C/60%HR, 30°C/65%HR, 30°C/75%HR, et 40°C/75%HR