N° 01 — Get in touch

Talk to a human,
not a form.

Choose the relevant route below. Include catalogue references and the requested document type where applicable so the team can review the correct scope.

N° 02 — Pick your route

How can we help?

I want to distribute

Apply to become a distribution partner in your territory.

→ Distributors

I have an OEM brief

Private-label or custom manufacturing enquiry.

→ OEM team

I need a regulatory document

IFU, DoC, TDS, material documentation, legacy letter, or vigilance contact.

→ Regulatory team

Something else

Procurement, press, partnerships, anything else.

→ General enquiries

N° 03 — Locations

Sialkot and request routes.

Sialkot Manufacturing HQ

32°29′N · 74°31′E

Headquarters

Sialkot, Pakistan

Kopek International (Pvt) Ltd
Plot No. 27/2, Street No. 03, Backside of Honda Falcon
Daska Road · Sialkot
Punjab, Pakistan

General

mail@kopek-international.com

Regulatory

Use request form below

EU Authorised Rep

Barcelona, Spain

AF Pharma Service Europe SL
Muntaner 281, 5º 1ª
Barcelona 08021

Regulatory requests routed below

Regulatory documents

Request by reference

Use the regulatory route for applicable IFU, TDS, DoC, material documentation, or authorized legacy-letter requests.

Catalogue reference required

OEM and distribution

Start with a brief

Share the target market, catalogue scope, expected volumes, and requested support through the relevant form.

Reviewed by enquiry type

N° 04 — General enquiries

Write to us.

If you are not sure which route fits, leave a message here and the team will review the enquiry internally.

GeneralGeneral enquiry review
DistributorsTerritory and portfolio review
OEMScope and feasibility review
RegulatoryDocuments routed by reference
VigilanceRequest appropriate contact

N° 05 — Regulatory enquiries

Documents & vigilance.

Use the Regulatory page for approved public IFU files and narrow public downloads. Request the applicable controlled TDS, DoC, material document, legacy-device confirmation letter or vigilance contact through this form.

IFU libraryApproved public files
TDSRequest by reference
DoCRequest applicable controlled file
Legacy letterAuthorization-only request
Audit supportReviewed by regulatory team

Request type

Name

Organisation

Verified distributor account ID (if applicable)

Reference(s) or available UDI-DI

Details

Controlled documents are routed after regulatory review. Include the relevant catalogue reference and requested document type.

N° 06 — OEM & Private label

Start a project.

Tell us what you would like to manufacture. Start with the target market, expected catalogue scope, branding model, packaging requirements, and document needs.

NDAAvailable on request
ScopeReviewed against your brief
FeasibilityConfirmed after review
SamplingDiscussed where applicable