Established since 1979
More than four decades of continuous trading relationships, regulatory familiarity and institutional memory in this market.
Accelerating access to
innovation.
We connect internationally approved pharmaceutical raw material manufacturers with finished-dose formulators across the region — bringing the marketing, sales, regulatory and technical expertise that makes every partnership work.
1979
Year founded
32
Therapeutic categories
220+
Molecules in portfolio
800+
Formulation manufacturers
150+
Principals represented
Rs. 1T+
Sector market value
Where do you fit?
Two sides of the same bridge.
Causeway exists to make one relationship work: the one between the people who make pharmaceutical raw materials and the people who turn them into medicine. Whichever side you are on, start here.
I manufacture raw materials
Reach a market of 800+ formulation manufacturers in one of Asia’s fastest-growing pharmaceutical sectors — without building a local operation.
For suppliers & principalsI manufacture finished dosage
Source qualified, regulator-approved raw materials from vetted manufacturers around the world, through one accountable partner.
For drug manufacturers
Who we are
A trusted link between manufacturers and formulators.
Since 1979, Causeway International has served the pharmaceutical industry from our headquarters in Karachi, with commercial reach across the country and the wider region. We provide marketing, sales, regulatory and technical services to global partners — acting as the vital link between international pharmaceutical raw material manufacturers and finished-dose formulation producers.
Our principals hold approvals from the world’s leading regulatory authorities — including US FDA, EDQM/CEP, WHO-GMP, EU-GMP and PMDA — and operate under strict cGMP conditions. We build long-term, transparent relationships grounded in integrity, accountability and results.
Why Causeway
Deep roots, broad capability.
Reach across the market
Headquartered in Karachi with active commercial coverage of the country’s manufacturing base and the wider region.
Regulatory fluency
Day-to-day familiarity with DRAP processes and the documentation regulated-market suppliers are expected to provide.
Document control
Shipping documents are checked against requirements the moment they arrive, corrections chased with the shipper, and clean sets passed to your team — so paperwork never holds a consignment up.
Let’s start a conversation.
Whether you are a raw material manufacturer looking for regional reach, or a formulator seeking a reliable supply partner — we would like to hear from you.