Regulated by the CFDD, Trinidad & Tobago requires detailed submissions and rigorous quality assurance standards. Whether you’re registering pharmaceuticals, veterinary products, or medical devices, Rebexa provides the local expertise and operational precision to move forward efficiently.
Clear the Path to Market in Trinidad & Tobago
Rebexa coordinates every step of the regulatory process with the Chemistry, Food & Drugs Division (CFDD), so your products can launch smoothly and remain compliant.
Strategic Regulatory Support for CFDD Compliance in Trinidad & Tobago.
What We Handle
- Product classification and dossier preparation
- Coordination with CFDD and supporting ministries
- Marketing authorization submission
- GMP, labelling, and packaging review
- Post-market variations, renewals, and withdrawals
We Support
- Prescription and OTC medications
- Veterinary drugs
- Medical devices and surgical instruments
- Personal care and hygiene products
- Disinfectants and household chemicals
Why Choose Rebexa
- End-to-end regulatory support with CFDD
- Local partnerships and in-country insight
- Cross-border coordination for Caribbean launches
- Agile and responsive regulatory consulting
Get Your Product Approved in Trinidad & Tobago Without the Hassle.
Start your market expansion with the right regulatory partner.
