Trinidad and Tobago

Caribbean

Contents

1. Regulatory Overview
2. Regulatory Pathways

Regulatory Overview

Trinidad and Tobago is regulated by the CDAP (Chemistry, Food and Drugs Division). The country has 1 documented regulatory pathway for accessing unapproved or unlicensed medicines, covering named patient programs, compassionate use schemes, and special access arrangements.

Regulatory Authority

CDAP (Chemistry, Food and Drugs Division)

Regulatory Pathways (1)

Trinidad and Tobago MOH Special Import Authorization 30 days

Trinidad and Tobago Ministry of Health special import authorization for unregistered medicines for patients with serious or life-threatening conditions.

Application Form: MOH Trinidad and Tobago Special Import Form

Legal Basis: Regulated

Eligibility: Serious or life-threatening condition with no locally registered alternative

Trinidad and Tobago

ISO Code	`TT`
Region	Caribbean
Regulatory Authority	CDAP (Chemistry, Food and Drugs Division)
Pathways	1 documented
Drugs Available	0 documented