Regulatory And Research Services for Hong-Kong
🇭🇰 Regulatory and Research Services for Hong Kong – 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 Hong Kong market.
Our services ensure full compliance with Hong Kong’s Department of Health (DoH), Drug Office regulations, local ordinances, and international ICH/WHO guidelines.
📘 Regulatory Services for Hong Kong
Regulatory & Product Registration Support – Hong Kong
We assist pharmaceutical, nutraceutical, and cosmetic companies at every stage of regulatory submission and product approval in Hong Kong, ensuring a smooth market entry and full compliance with DoH 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 Hong Kong registration.
• Support in API regulatory documentation, including quality, safety, and stability data.
⚗️ Bioequivalence (BE) Study Support
• Design and coordination of BE studies in DoH-approved CROs.
• Preparation of complete BE study reports in accordance with WHO and Hong Kong 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 Hong Kong.
• Assistance with import/export permissions, DoH inspections, and post-approval compliance.
• Regular updates on DoH and WHO regulatory changes to ensure continuous product compliance.
🧪 Research & Development (R&D) Services – Hong Kong
Our R&D services support your product development, validation, and quality assurance activities in compliance with Hong Kong’s DoH 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 DoH requirements.
🧍⚕️ Clinical Trial & Toxicology Support
• Preparation of clinical trial protocols and final study reports.
• Toxicological evaluation in compliance with OECD and DoH guidelines.
🌏 Why Choose Us for the Hong Kong Market
• Experienced Team – Experts in DoH, 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
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⚗️ Bioequivalence & Analytical Studies
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🧪 Technology Transfer & Safety
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