Science & Quality
Developed, made, tested, released — and watched after it reaches a patient.
The journey
From molecule to patient
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Stability
Two years, on the clock
Held at 40°C ± 2°C and 75% ± 5% relative humidity (Zone IVB) — the accelerated condition for the climate our products actually ship into.
3
mo
6
mo
12
mo
24
mo
Control samples from every batch manufactured are held in an environmentally controlled repository for verification against any market complaint.
Pharmacovigilance
What we commit to, in writing
- Serious adverse event escalated Within 24 hours.
- Any report acknowledged Within 48 hours.
- Substantive response given Within 15 days.
Standards
What a batch is measured against
- IP
- BP
- USP
Indian, British and United States Pharmacopoeia monographs.
We partner with manufacturing plants approved under the World Health Organization's Good Manufacturing Practices (WHO-GMP) and the DCGI. Products are manufactured in sterile, humidity-controlled cleanrooms using automated machinery, and pilot batches are validated before mass manufacturing begins.
On the QC bench
- High-performance liquid chromatography (HPLC)
- Dissolution apparatus
- Disintegration apparatus
- Tablet hardness tester
- Friability tester
- Viscometer for gels and sprays
- Fill-weight and uniformity check station
- Packaging material testing — thickness, tensile strength and pinhole leak
- Environmental stability chambers
In detail
