Regulatory And Research Services for Moldova

๐Ÿ‡ฒ๐Ÿ‡ฉ 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.

๐Ÿ“˜ 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.

๐Ÿ“˜ Product Registration Services
โ€ข Preparation and submission of export registration dossiers for prescription (Rx) and OTC products.
โ€ข Registration support for Herbal, Ayurveda, Nutraceutical, Veterinary, and Cosmetic products.
โ€ข Guidance on local labeling, packaging requirements, and product information leaflets.

๐Ÿ“— Drug Master File (DMF) Services
โ€ข Compilation of CTD/ACTD-compliant DMFs for APIs intended for Moldova registration.
โ€ข Support in API regulatory documentation, including quality, safety, and stability data.

โš—๏ธ Bioequivalence (BE) Study Support
โ€ข Design and coordination of BE studies in NAMDM-approved CROs.
โ€ข Preparation of complete BE study reports in accordance with WHO and Moldova regulatory requirements.

๐Ÿ”ฌ Analytical Method Validation (AMV) Services
โ€ข Validation of analytical methods as per ICH Q2(R2) guidelines.
โ€ข Preparation of AMV documentation for regulatory submission and routine QC support.

๐Ÿงพ Regulatory Consultancy & Compliance
โ€ข Comprehensive regulatory guidance for export or local market entry in Moldova.
โ€ข Assistance with import/export permissions, NAMDM inspections, and post-approval compliance.
โ€ข Regular updates on NAMDM and WHO regulatory changes to ensure continuous product compliance.

๐Ÿงช Research & Development (R&D) Services โ€“ Moldova
Our R&D services support your product development, validation, and quality assurance activities in compliance with Moldovaโ€™s NAMDM and international standards.

๐Ÿ’Š Formulation Development
โ€ข Development of tablets, capsules, syrups, powders, and injectables.
โ€ข Optimization for stability, bioavailability, and efficacy suited to regional conditions.

๐Ÿงซ Analytical R&D Services
โ€ข Assay, dissolution, impurity profiling, and stability testing.
โ€ข Quality control method development and routine analytical testing.

๐Ÿ“‘ Product Development Reports (PDRs)
โ€ข Preparation of comprehensive PDRs for regulatory submission.
โ€ข Inclusion of manufacturing process, QC methods, and stability data in line with NAMDM requirements.

๐Ÿงโ€โš•๏ธ Clinical Trial & Toxicology Support
โ€ข Preparation of clinical trial protocols and final study reports.
โ€ข Toxicological evaluation in compliance with OECD and NAMDM guidelines.

๐ŸŒ Why Choose Us for the Moldovan Market
โ€ข Experienced Team โ€“ Experts in NAMDM, WHO, and ICH regulatory frameworks.
โ€ข End-to-End Support โ€“ From formulation development to market registration and post-approval compliance.
โ€ข Global Exposure โ€“ Proven experience across ROW, ASEAN, US, and EU markets.
โ€ข Timely Submissions โ€“ Streamlined processes ensuring faster approvals.
โ€ข Custom Solutions โ€“ Tailored strategies for your product type, market, and regulatory pathway.

๐Ÿ“˜ Regulatory & Dossier Documentation โ€“ Moldova
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โš—๏ธ Bioequivalence & Analytical Studies โ€“ Moldova
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๐Ÿงช Technology Transfer & Safety โ€“ Moldova
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๐ŸŒ Top Pharma & Regulatory Hashtags โ€“ Moldova
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