Global Product Development Report (PDR) Services – Pharma
For Pharmaceutical Companies Supplying to Sri Lanka
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, review, and lifecycle support for pharmaceutical manufacturers and exporters supplying medicinal products to Sri Lanka.
Since 2008, we have successfully prepared and reviewed 600+ Product Development Reports (PDRs) for pharmaceutical companies across Asia, Middle East, Africa, Europe, and LATAM, ensuring robust scientific justification, 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 regulatory 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 & tender readiness
Our Core PDR Services – Sri Lanka Focus
📘 Product Development Report (PDR) Documentation
Complete PDR Protocol preparation
PDR Report writing with strong scientific & regulatory justification
Development rationale for QTPP, CQA, CMA & CPP
Comparative formulation development & optimization studies
Excipient selection and compatibility justification
Scale-up strategy & manufacturing readiness justification
🔍 PDR Review & Gap Assessment
Independent technical and regulatory review of existing PDRs
Gap assessment against ICH, CTD & Sri Lanka authority expectations
Identification of scientific, data & compliance gaps
Authority-focused restructuring of PDR content
📊 Backup Data Compilation & Presentation
Compilation of complete development backup data
Lab-scale, pilot-scale & exhibit batch data
Dissolution development & comparative profiles
Stability development data (where applicable)
Process optimization & robustness studies
📨 Regulatory Query Handling (Post-Submission)
Responses to National Medicines Regulatory Authority (NMRA), Sri Lanka queries
Scientific justification for development-related deficiencies
Post-submission & post-approval support
Lifecycle updates to 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 & Technical Alignment
Our PDRs for Sri Lanka–bound products are prepared in line with:
ICH Guidelines (Q8, Q9, Q10, Q11)
CTD / eCTD dossier expectations
WHO Technical Report Series (TRS)
Sri Lanka NMRA registration requirements
Export market expectations for South Asia, ASEAN & ROW
Industries We Serve
Pharmaceutical Finished Dosage Form manufacturers
Export-oriented pharma companies
Contract manufacturers & CDMOs
Regulatory affairs & dossier consultancies
Brand owners & Marketing Authorization Holders (MAHs)
Why Companies Supplying to Sri Lanka Choose ProdDev
✅ 600+ PDRs prepared & reviewed globally
✅ Strong experience with South Asian & NMRA-aligned registrations
✅ Authority-ready, science-driven documentation
✅ Integrated R&D, QA & Regulatory Affairs expertise
✅ End-to-end lifecycle & post-approval support
✅ Confidential, reliable & deadline-driven execution
Our Proven PDR Execution Approach
Product understanding & scope finalization
Regulatory & development requirement mapping
PDR Protocol preparation / review
Scientific PDR Report writing with complete backup data
Independent QA & regulatory review
Submission-ready delivery & NMRA query support
Who We Work With
We support companies supplying medicines to:
Sri Lanka | South Asia | ASEAN | Middle East | Africa | LATAM
From essential medicines and tenders to imported branded generics, our PDRs are designed to be inspection-ready and authority-acceptable.
Confidentiality & Compliance
All projects are handled under strict:
Confidentiality & non-disclosure agreements
Data integrity & ALCOA+ principles
GMP & global regulatory compliance standards
Get in Touch
Looking for PDR Protocol & Report preparation, review, or regulatory query support for pharmaceutical products supplied to Sri Lanka?
📩 Contact ProdDev – Product Development Experts
A Scientific Arm of Zoesoe Exports Pvt. Ltd.
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