🇷🇼 Analytical Method Validation Services – Rwanda

Ensuring Accuracy. Compliance. Regulatory Confidence for Rwanda Regulatory Submissions

VALIDEX, a scientific arm of Zoesoe Exports Pvt Ltd, provides end-to-end Analytical Method Validation (AMV) services for Active Pharmaceutical Ingredients (APIs) and Pharmaceutical Finished Products in full compliance with Rwanda's regulatory requirements.

We support pharmaceutical manufacturers and suppliers across Rwanda with compliance aligned with the Rwanda Food and Drugs Authority (Rwanda FDA), ICH-aligned documentation, and post-submission handling of Rwanda FDA queries for drug registration, licensing, and import/export requirements.

🇷🇼 Our Core Expertise – Rwanda Focus

VALIDEX offers comprehensive preparation, review, and regulatory support for Analytical Method Validation as required by the Rwanda FDA and internationally accepted pharmacopoeial standards, often following guidelines from WHO and regional East African Community (EAC) harmonization efforts.

  • ✅ Assay Method Validation

    • Potency and content determination

    • Validation as per ICH Q2 (R1 / R2) aligned with Rwanda FDA and EAC quality expectations

    • Accuracy, precision, linearity, robustness, and specificity

    • BP/USP/EP harmonized methods

  • ✅ Impurities Method Validation

    • Related substances & degradation product profiling

    • Identification and quantification of impurities

    • Stability-indicating method validation as per ICH and WHO-GMP

  • ✅ Dissolution Method Validation

    • Immediate & modified release products

    • Discriminatory dissolution method development

    • Media selection, sink condition assessment, and method robustness

    • Compliance with product registration requirements, following EAC/international norms (CTD format).

  • ✅ Residual Solvents Method Validation

    • Gas Chromatographic (GC) method validation

    • Compliance with ICH Q3C adopted globally, aligning with Rwanda FDA's quality expectations

    • Class I, II & III residual solvents

    • Limits, system suitability, accuracy, and precision

🇷🇼 Products Covered – Rwanda

  • ✅ Active Pharmaceutical Ingredients (APIs)

  • ✅ Oral solid dosage forms (tablets, capsules, sachets)

  • ✅ Injectable formulations (sterile & non-sterile)

  • ✅ Semi-solid & liquid dosage forms

  • ✅ Modified & controlled release products

🇷🇼 Regulatory Compliance – Rwanda

All Analytical Method Validation activities are conducted in accordance with:

  • ICH Q2 (R1 / R2)

  • Rwanda FDA Guidelines and national pharmaceutical regulations

  • WHO-GMP recommendations, widely accepted in the region

  • East African Community (EAC) Harmonized Guidelines

  • United States Pharmacopeia (USP)

  • European Pharmacopoeia (EP)

  • British Pharmacopoeia (BP)

🇷🇼 Post-Submission Regulatory Support (Rwanda)

VALIDEX provides complete regulatory query management, assisting with responses to the Rwanda FDA and other competent authorities, including:

  • ✅ Response to regulatory deficiency letters

  • ✅ Scientific justification for validation parameters

  • ✅ Data gap assessment & corrective documentation

  • ✅ Revised validation protocols and reports

  • ✅ Technical support during regulatory inspections & audits

🇷🇼 Why Choose VALIDEX for Rwanda?

  • ✔ Strong understanding of Rwanda's FDA regulatory expectations and regional EAC standards

  • ✔ ICH-aligned documentation focused on African and international compliance norms

  • ✔ Inspection-ready and audit-compliant validation reports

  • ✔ Fast turnaround timelines

  • ✔ Strict confidentiality & data integrity

  • ✔ Single-window scientific and regulatory support under Zoesoe Exports Pvt Ltd

🇷🇼 Our Deliverables – Rwanda

  • Analytical Method Validation Protocols (Rwanda FDA-compliant)

  • Validation Reports for:

    • Assay

    • Impurities

    • Dissolution

    • Residual Solvents

  • CTD / Non-CTD summary documents for Rwanda FDA submissions

  • Regulatory query response packages

  • Method transfer & verification documentation

🇷🇼 Industries We Serve in Rwanda

  • Pharmaceutical manufacturing companies

  • API traders and importers

  • Generic formulation companies

  • Contract Manufacturing Organizations (CMOs)

  • Import and Distribution companies

  • Regulatory & dossier consulting firms

🇷🇼 National & Export Support

VALIDEX supports Analytical Method Validation for:

  • Rwanda domestic approvals (Market Authorization from Rwanda FDA)

  • Manufacturing licenses & product permissions

  • Export dossiers for regional (EAC) and international shipment from Rwanda

🇷🇼 Partner with VALIDEX – Rwanda

Achieve Rwanda FDA-ready analytical validation with confidence.

From method validation to regulatory approvals, VALIDEX is your trusted scientific and regulatory partner in Rwanda.