ProdDev – Global Product Development Report (PDR) Services for Fiji
Regulatory-Compliant | Authority-Ready | Globally Trusted
ProdDev, a scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Product Development Report (PDR) Protocol & Report preparation and review services for pharmaceutical companies operating in Fiji and supplying to domestic, Pacific regional, and international markets.
Since 2008, we have successfully prepared and reviewed 600+ Product Development Reports (PDRs) for pharmaceutical manufacturers, exporters, and regulatory teams across Asia, Middle East, Africa, Europe, LATAM, and Oceania, ensuring scientific robustness, regulatory compliance, and authority acceptance.
Who We Are
ProdDev is a specialized pharmaceutical product development documentation service provider, focused exclusively on PDR Protocol & Report preparation, review, and full lifecycle support.
Our multidisciplinary team includes:
Pharmaceutical formulation scientists
Regulatory affairs professionals
QA & GMP experts
Technical documentation specialists
We bridge the gap between:
Formulation development → Scale-up → Regulatory submission
R&D data → Authority-acceptable documentation
Development stage → Commercial manufacturing readiness
Our Core PDR Services – Fiji (Pharma)
📘 Product Development Report (PDR) Documentation
Complete PDR Protocol preparation
Scientific PDR Report writing with strong development rationale
Justification for QTPP, CQA, CMA & CPP
Comparative formulation development & optimization studies
Excipient selection & compatibility justification
Scale-up and manufacturing readiness documentation
🔍 PDR Review & Gap Assessment
Independent technical & regulatory review of existing PDRs
Gap assessment against ICH, CTD & Fiji MOH–aligned requirements
Risk identification with corrective & preventive recommendations
Authority-focused restructuring to improve approval outcomes
📊 Backup Data Compilation & Presentation
Compilation of complete development backup data
Lab-scale, pilot-scale & exhibit batch summaries
Dissolution development & comparative profiles
Stability development data (as applicable)
Process optimization & robustness documentation
📨 Regulatory Query Handling (Post-Submission)
Fiji Ministry of Health & Medical Services (MHMS) PDR-related query responses
Scientific justification for development deficiencies
Post-submission & post-inspection support
Lifecycle maintenance & updates of PDR documentation
Dosage Forms We Support
Tablets (IR, MR, ER, DR)
Capsules (Hard gelatin, HPMC)
Oral liquids & suspensions
Powders & granules
Topical & semi-solid formulations
Sterile & non-sterile products (documentation support)
Fixed Dose Combinations (FDCs)
Regulatory Alignment for Fiji & Export Markets
Our PDRs are prepared in alignment with:
ICH Guidelines (Q8, Q9, Q10, Q11)
CTD / eCTD dossier structures
WHO Technical Report Series (TRS)
Fiji Ministry of Health & Medical Services expectations
PIC/S & WHO-prequalified frameworks (where applicable)
Australia, New Zealand, ASEAN, GCC & ROW export requirements
Industries We Serve in Fiji
Pharmaceutical finished dosage manufacturers
Importers & marketing authorization holders
Government & hospital supply organizations
Contract manufacturers & CDMOs
Regulatory affairs & compliance consultancies
Why Fiji-Based Clients Choose ProdDev
✅ 600+ PDRs successfully prepared & reviewed
✅ Strong experience with small & emerging regulatory markets
✅ Authority-ready, science-driven documentation
✅ Integrated R&D, QA & Regulatory expertise
✅ End-to-end lifecycle & authority query support
✅ Strict confidentiality & data integrity
Our Structured Approach
Product understanding & scope finalization
Regulatory & development requirement mapping (Fiji & export markets)
PDR Protocol preparation / review
Scientific PDR Report writing with complete backup data
Independent QA & regulatory review
Submission-ready delivery & post-submission support
Who We Work With
We support Fiji-based companies supplying to:
Domestic MHMS registrations | Pacific Islands | Australia & New Zealand | Asia | Africa | LATAM
Our PDRs are designed to be inspection-ready, regulator-friendly, and submission-acceptable.
Confidentiality & Compliance
All projects are handled under strict:
Confidentiality agreements
Data integrity principles
GMP & international regulatory compliance standards
Get in Touch
Looking for PDR Protocol & Report preparation, review, or Fiji MHMS regulatory query support for your pharmaceutical products?
📩 Contact ProdDev – Product Development Experts
A Scientific Arm of Zoesoe Exports Pvt. Ltd.