Regulatory And Research Services for Moldova
๐ฒ๐ฉ Regulatory and Research Services for Moldova โ 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 Moldovan market.
Our services ensure full compliance with the National Agency for Medicines and Medical Devices of Moldova (NAMDM) regulations, national standards, and international ICH/WHO guidelines.
๐ Regulatory Services for Moldova
Regulatory & Product Registration Support โ Moldova
We assist pharmaceutical, nutraceutical, and cosmetic companies at every stage of regulatory submission and product approval in Moldova, ensuring a smooth market entry and full compliance with NAMDM guidelines.
๐ Product Registration Services
โข Preparation and submission of export registration dossiers for prescription (Rx) and OTC products.
โข Registration support for Herbal, Ayurveda, Nutraceutical, Veterinary, and Cosmetic products.
โข Guidance on local labeling, packaging requirements, and product information leaflets.
๐ Drug Master File (DMF) Services
โข Compilation of CTD/ACTD-compliant DMFs for APIs intended for Moldova registration.
โข Support in API regulatory documentation, including quality, safety, and stability data.
โ๏ธ Bioequivalence (BE) Study Support
โข Design and coordination of BE studies in NAMDM-approved CROs.
โข Preparation of complete BE study reports in accordance with WHO and Moldova regulatory requirements.
๐ฌ Analytical Method Validation (AMV) Services
โข Validation of analytical methods as per ICH Q2(R2) guidelines.
โข Preparation of AMV documentation for regulatory submission and routine QC support.
๐งพ Regulatory Consultancy & Compliance
โข Comprehensive regulatory guidance for export or local market entry in Moldova.
โข Assistance with import/export permissions, NAMDM inspections, and post-approval compliance.
โข Regular updates on NAMDM and WHO regulatory changes to ensure continuous product compliance.
๐งช Research & Development (R&D) Services โ Moldova
Our R&D services support your product development, validation, and quality assurance activities in compliance with Moldovaโs NAMDM and international standards.
๐ Formulation Development
โข Development of tablets, capsules, syrups, powders, and injectables.
โข Optimization for stability, bioavailability, and efficacy suited to regional conditions.
๐งซ Analytical R&D Services
โข Assay, dissolution, impurity profiling, and stability testing.
โข Quality control method development and routine analytical testing.
๐ Product Development Reports (PDRs)
โข Preparation of comprehensive PDRs for regulatory submission.
โข Inclusion of manufacturing process, QC methods, and stability data in line with NAMDM requirements.
๐งโโ๏ธ Clinical Trial & Toxicology Support
โข Preparation of clinical trial protocols and final study reports.
โข Toxicological evaluation in compliance with OECD and NAMDM guidelines.
๐ Why Choose Us for the Moldovan Market
โข Experienced Team โ Experts in NAMDM, WHO, and ICH regulatory frameworks.
โข End-to-End Support โ From formulation development to market registration and post-approval compliance.
โข Global Exposure โ Proven experience across ROW, ASEAN, US, and EU markets.
โข Timely Submissions โ Streamlined processes ensuring faster approvals.
โข Custom Solutions โ Tailored strategies for your product type, market, and regulatory pathway.
๐ Regulatory & Dossier Documentation โ Moldova
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โ๏ธ Bioequivalence & Analytical Studies โ Moldova
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๐งช Technology Transfer & Safety โ Moldova
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