SUPPLY CHAIN
Generic pharmaceuticals, sourced to GMP standard.
Qualified producers, verified dossiers and documented delivery — generic drug supply managed end to end, from the site audit to the released batch.
Services
9 DISCIPLINES01
Producer Qualification
On-site audits and GMP certificate verification.
02
Product Sourcing
Finished dose and API against your specification.
03
Regulatory Dossiers
CTD, CEP and ASMF documentation assembled.
04
Quality Agreements
Responsibilities defined between site and buyer.
05
Batch Documentation
CoA, CoC and batch records checked per shipment.
06
Import & Licensing
Permits, declarations and customs clearance.
07
Cold Chain Logistics
GDP-compliant, temperature-monitored transport.
08
Serialization
Track-and-trace coding to destination-market rules.
09
Supply Continuity
Dual sourcing, stock cover and shortage response.
See what we supply.
Active substance, strength, dosage form and therapeutic area for every product we carry. Producer, GMP standard, registered markets and lead times are available to signed-in clients.
Process
1
Qualification
Audit and approve the producer.
2
Specification
Product, market and volume defined.
3
Documentation
Dossiers, licences and agreements.
4
Validation
Sample testing and first-batch review.
5
Shipment
GDP transport and customs clearance.
6
Ongoing Supply
Scheduled batches and monitoring.
PHILOSOPHY
A generic is only as good as the site that made it and the paper trail behind it. Lithos qualifies producers on the ground, keeps the regulatory file current, and treats every batch as evidence — so what reaches your market is traceable to its origin.
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