FDA Compliance
Our commitment to regulatory standards and patient safety.
Quick Pharma operates in full compliance with the Drugs and Cosmetics Act, 1940, and the rules framed thereunder, as well as applicable guidelines from the Central Drugs Standard Control Organisation (CDSCO) and relevant State Drug Authorities.
business Licensed Pharmacy Operations
Quick Pharma holds valid drug licenses issued under the Drugs and Cosmetics Act. All retail and wholesale operations are conducted under the supervision of registered pharmacists as mandated by law. Our license details are available for inspection upon request by regulatory authorities.
inventory_2 Product Sourcing & Storage
Every product in our catalog is sourced exclusively from licensed manufacturers and authorised distributors. We do not stock counterfeit, sub-standard, or spurious drugs. Our storage facilities maintain:
- thermometer Temperature-controlled environments per product-specific storage requirements.
- humidity_high Humidity monitoring to preserve product integrity.
- package_2 Segregated storage for Schedule H, H1, and X drugs.
- inventory Regular batch-level inventory audits and expiry checks.
assignment Prescription Verification
All prescription (Schedule H, H1, and X) medicines are dispensed only after verification by our licensed pharmacist team. Our verification process includes:
- check_circle Validation of prescriber's registration number and signature.
- check_circle Confirmation that the prescription is current and issued in the patient's name.
- check_circle Cross-referencing dosage and quantity against safe prescribing guidelines.
- check_circle Retention of prescription records as required by the Drugs and Cosmetics Rules.
local_shipping Cold Chain & Dispatch
Products requiring cold-chain logistics (e.g., certain biologics, insulins, vaccines) are packed and dispatched with validated temperature-monitoring packaging. Our logistics partners are briefed on cold-chain handling requirements to ensure product efficacy upon delivery.
report Adverse Drug Reaction Reporting
Quick Pharma participates in the Pharmacovigilance Programme of India (PvPI). If you experience an unexpected or severe reaction to any product purchased from us, we encourage you to report it to your doctor and notify our pharmacist team via our contact page. We will ensure the report is forwarded to the appropriate regulatory authority.
policy Data Protection
Prescription data and personal health information are handled in accordance with applicable data protection laws. Access is restricted to licensed pharmacists and authorized personnel directly involved in order fulfillment. All digital records are encrypted and retained for the period mandated by the Drugs and Cosmetics Rules.
For regulatory queries or to report a compliance concern, contact our Regulatory Affairs team via our contact page. We are committed to full transparency with regulatory authorities.