Regulatory And Research Services for Trinidad-and-Tobago
🇹🇹 Regulatory and Research Services for Trinidad and Tobago – Dossier-DMF Services @ Zoesoe Exports Pvt Ltd
We, Zoesoe Exports Pvt Ltd, specialize in providing end-to-end regulatory and research solutions to pharmaceutical, nutraceutical, herbal, and cosmetic companies aiming to enter the Trinidad and Tobago market.
Our services ensure full compliance with the Trinidad and Tobago Ministry of Health – Drug Inspectorate, Health Sciences Authority (HSA) regulations, national standards, and international ICH/WHO guidelines.
📘 Regulatory Services for Trinidad and Tobago
Regulatory & Product Registration Support – Trinidad and Tobago
We assist pharmaceutical, nutraceutical, and cosmetic companies at every stage of regulatory submission and product approval in Trinidad and Tobago, ensuring a smooth market entry and full compliance with HSA guidelines.
📘 Product Registration Services
• Preparation and submission of export registration dossiers for prescription (Rx) and OTC products.
• Registration support for Herbal, Ayurveda, Nutraceutical, Veterinary, and Cosmetic products.
• Guidance on local labeling, packaging requirements, and product information leaflets.
📗 Drug Master File (DMF) Services
• Compilation of CTD/ACTD-compliant DMFs for APIs intended for Trinidad and Tobago registration.
• Support in API regulatory documentation, including quality, safety, and stability data.
⚗️ Bioequivalence (BE) Study Support
• Design and coordination of BE studies in HSA-approved CROs.
• Preparation of complete BE study reports in accordance with WHO and Trinidad and Tobago regulatory requirements.
🔬 Analytical Method Validation (AMV) Services
• Validation of analytical methods as per ICH Q2(R2) guidelines.
• Preparation of AMV documentation for regulatory submission and routine QC support.
🧾 Regulatory Consultancy & Compliance
• Comprehensive regulatory guidance for export or local market entry in Trinidad and Tobago.
• Assistance with import/export permissions, HSA inspections, and post-approval compliance.
• Regular updates on HSA and WHO regulatory changes to ensure continuous product compliance.
🧪 Research & Development (R&D) Services – Trinidad and Tobago
Our R&D services support your product development, validation, and quality assurance activities in compliance with Trinidad and Tobago HSA and international standards.
💊 Formulation Development
• Development of tablets, capsules, syrups, powders, and injectables.
• Optimization for stability, bioavailability, and efficacy suited to regional conditions.
🧫 Analytical R&D Services
• Assay, dissolution, impurity profiling, and stability testing.
• Quality control method development and routine analytical testing.
📑 Product Development Reports (PDRs)
• Preparation of comprehensive PDRs for regulatory submission.
• Inclusion of manufacturing process, QC methods, and stability data in line with HSA requirements.
🧍⚕️ Clinical Trial & Toxicology Support
• Preparation of clinical trial protocols and final study reports.
• Toxicological evaluation in compliance with OECD and HSA guidelines.
🌏 Why Choose Us for the Trinidad and Tobago Market
• Experienced Team – Experts in HSA, WHO, and ICH regulatory frameworks.
• End-to-End Support – From formulation development to market registration and post-approval compliance.
• Global Exposure – Proven experience across ROW, ASEAN, US, and EU markets.
• Timely Submissions – Streamlined processes ensuring faster approvals.
• Custom Solutions – Tailored strategies for your product type, market, and regulatory pathway.
📘 Regulatory & Dossier Documentation – Trinidad and Tobago
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