Middle East · Türkiye · CIS · Global admin@adapharmaco.com
Quality & Documentation

Full documentation from qualified manufacturers.

With 7 years of experience and 3 CPHI exhibition presences, Adapharma coordinates documentation from qualified manufacturers worldwide. We started with industrial spare parts documentation and expanded to full pharmaceutical sourcing. CoA, MSDS, and TDS are always available. CEP, DMF, GMP, FDA certifications available on request per manufacturer.

9Active products
9From GMP manufacturers
4DMF available
6CEP available

Always coordinated documents

These documents come with every shipment, coordinated from the original manufacturer.

CoA
Certificate of Analysis With every shipment
MSDS
Safety Data Sheet With every product
TDS
Technical Data Sheet Full specifications

Manufacturer certifications (on request)

These certifications belong to original manufacturers — we request them for you as needed. Availability depends on the manufacturer per product.

EU
GMP
EU-GMP on request
WHO
GMP
WHO-GMP on request
ISO
9001
ISO 9001 on request
FDA
DMF
US FDA DMF on request
CEP
EDQM
CEP / EDQM on request

Documentation availability matrix

Shows which manufacturer certifications are available for each product in our catalog.

Product
DMF
CEP
US FDA
EU GMP
WHO-GMP
✓ = Original manufacturer certification available on request

Documentation process

01

Qualified manufacturer selection

We select manufacturers with appropriate certifications for your market requirements before accepting the order.

02

Document request

We request CoA, MSDS, TDS from the manufacturer for every batch. Regulatory docs on request.

03

Verification & delivery

All documents verified before delivery. Stored in your customer portal.

Get started

The documentation you need is one contact away.

Contact our team to discuss documentation requirements specific to your market.

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