DCGI
Drug Controller General of India — central authority for pharmaceutical approvals.
Beyond compliance — quality is embedded in every product we supply, every process we follow, and every partnership we build.
At Layte LifeScience, quality is not an afterthought — it is the foundation. We source exclusively from manufacturers who meet the highest national and international regulatory standards, and we conduct our own verification before any product enters our supply chain.
We believe that every medicine we distribute has a patient at the end. That responsibility drives us to maintain zero tolerance for substandard products.
Our products and suppliers are approved and registered under the following regulatory bodies:
Drug Controller General of India — central authority for pharmaceutical approvals.
Central Drugs Standard Control Organisation oversight for drug quality and safety.
World Health Organisation Good Manufacturing Practice aligned manufacturing partners.
Quality Management System frameworks for consistent, auditable processes.
Strict legal compliance and operational audits under the Indian Drugs and Cosmetics Act and international FDA regulations, as authorized by our MoA.
Wholesale distribution and chemical trading license issued by the Drugs Control Department, Government of NCT of Delhi.
Fully compliant GST-registered entity with proper invoice documentation.
We audit every manufacturer's regulatory status before onboarding.
Every shipment includes CoA, manufacturer license, and batch records.
Temperature-sensitive products handled with cold-chain logistics.
Full traceability from manufacturer to customer with invoice documentation.
“We do not just sell medicines — we supply trust. Our customers rely on us not just for product availability, but for the assurance that every unit meets the standard their patients deserve.”
— Director, Layte LifeScience Pvt. Ltd.