Quality Commitment
Quality at the Heart of Healthcare
At Gift Pharma, quality is more than a standard; it is our primary operating metric. We realize that the drugs we source and formulate impact patient lives. Therefore, we integrate thorough testing, stability evaluations, and packaging validation checks into our workflows.
Our quality management system oversees compound validation, sterile atmosphere controls, batch record checks, and storage temperature audits.
Our Quality Verification Processes
Raw Material Audits
We screen active pharmaceutical ingredients (API) to ensure they are free from impurities and meet reference parameters before starting formulation.
In-Process Controls
Every batch is monitored during the packaging and formulation phases, checking size margins, dissolution periods, and moisture limits.
Stability Evaluations
Retained batch samples are stored in specialized environmental chambers to study shelf-life stability across various climate conditions.