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We undertake raw material and finished product analysis as per the International Standards (British Pharmacopoeia and United States Pharmacopoeia).

Through continuous inspection of Pharmaceutical and Non-Pharmaceutical products, we aim to take on our role in assuring widespread community health by the reduction of counterfeit products in the market.

Among the tests carried out include Assay Identification by High Performance Liquid Chromatography (HPLC), Gas Chromatography- Mass Spectrophotometer (GC-MS), Liquid Chromatography Mass Spectrophotometer (LC-MS), Atomic Absorption Spectroscopy (AAS), UV/VIS Microbial Identification and Bioassay.

Parameters tested for:

01. Pharmaceutical finished product analysis:

01
01

Assay by HPLC, Assay by UV. VIS spectrophotometer, Assay by Titration, Dissolution test, Loss on drying. Identification (pH, melting point , FTIR and by IR), etc

02
02

ELEMENTAL ANALYSIS BY AAS (Sodium, Copper, Zinc, Calcium, Iron, Magnesium, Selenium, Potassium, Chromium, Nickel, Cadmium, Lead, Manganese), etc

03
03

Microbial identification, Microbial Bio assay, etc

02. Pharmaceutical raw product analysis

01
01

Assay by HPLC, Assay by UV. VIS spectrophotometer, Assay by Titration, Identification (pH, melting point, FTIR and by IR), etc

02
02

ELEMENTAL ANALYSIS BY AAS (Sodium, Copper, Zinc, Calcium, Iron, Magnesium, Selenium, Potassium, Chromium, Nickel, Cadmium, Lead, Manganese), etc

03
03

Microbial identification, etc

Sampling Guide
Sampling Guide


A minimum volume of 20 tablets/capsules, 2 suspensions/syrup bottles and 100g of raw materials is advisable for each requested test. Samples should be brought in before 10am for the turnaround time to begin on the sample submission day.
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