Raw Material Testing
Every incoming ingredient is verified for identity, purity and specification before it is ever used.
Trust, Tested At Every StepIndependent quality control and assurance overseeing every batch — from incoming raw material to finished, released pack.
At Aurika, an independent Quality Control and Quality Assurance function oversees every batch — from incoming raw material to finished, released pack.
Our laboratories are equipped to test identity, purity, potency, dissolution and stability against established pharmacopoeial standards, so that every dose performs exactly as intended.
Every incoming ingredient is verified for identity, purity and specification before it is ever used.
Continuous monitoring during production — weight, hardness, thickness, disintegration.
Assay, dissolution, uniformity and microbial testing on every finished batch.
Real-time and accelerated studies confirm shelf-life across climatic conditions.
Complete batch records enable full traceability from source to patient.
No batch is dispatched without independent Quality Assurance sign-off.
We hold ourselves to a single, uncompromising measure: the gold standard.
Manufacturing aligned to World Health Organization Good Manufacturing Practice.
Documented quality management across the organisation.
Good manufacturing and laboratory practice embedded in daily work.
Exact certificate numbers and issuing bodies to be listed once finalised.
Because Aurika supplies diverse international regions spanning multiple climatic zones, stability is non-negotiable. Our products are studied under relevant climatic-zone conditions to confirm that they remain safe and fully effective — from the day they are made to the day they are taken.
Certifications set the floor; culture sets the standard.
At Aurika, quality is owned by everyone — from the operator on the line to the analyst in the lab — because we never forget that a real person is waiting on the other side of every batch.
A Culture of Quality