Our Quality Commitment
Medgraaft operates under a zero-compromise, two-tier Quality Assurance and Control system to guarantee patient safety and formulation efficacy.
Quality Assurance (QA)
Our QA team ensures that standard operating procedures (SOPs) are strictly observed across partner plants. They handle systemic audits, validation logs, batch record clearances, and verify cleanroom airflow dynamics (HVAC systems).
Quality Control (QC)
Our analytical laboratories handle rigorous physical and chemical inspections. Sourced active pharmaceutical ingredients (APIs) undergo chromatography (HPLC), dissolution tests, and microbiological sterility checks to ensure absolute safety.
Regulatory Compliance
We ensure all therapeutic molecules compile with global pharmacopoeias (IP, BP, USP). Our manufacturing affiliates maintain active WHO-GMP certificates, COAs (Certificates of Analysis), and ISO 9001:2015 validations.
Batch Traceability
We maintain clear records for every manufactured lot. In compliance with drug controller rules, we index batch numbers, raw material sources, in-process logs, and shipping destinations for absolute tracking security.
Vendor Selection & Audits
We source active substances and packaging films exclusively from pre-vetted, ISO certified chemical synthesizers. Our procurement experts run periodic physical audits to verify vendor material integrity.
Continuous Customer Satisfaction
We operate a dedicated Pharmacovigilance and complaint desk. Patient feedbacks, distributor reports, and product stability comments are logged and resolved promptly to maintain highest standards.