Global Product Development Report (PDR) Services – Pharma

For Pharmaceutical Companies in the UAE

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 regulatory support services for pharmaceutical manufacturers, importers, distributors, and marketing authorization holders in the United Arab Emirates.

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 technical accuracy, regulatory compliance, and smooth acceptance by health authorities.

Importance of PDR for UAE Pharma Companies

For pharmaceutical companies operating in the UAE, a scientifically robust Product Development Report (PDR) is essential for:

• MOHAP (Ministry of Health & Prevention) product registration

• Dubai Health Authority (DHA) & Abu Dhabi DoH technical evaluations

• Import licensing, renewals & post-approval variations

• GCC regional registrations and reliance pathways

• Readiness for WHO, PIC/S & international GMP inspections

ProdDev delivers science-driven, MOHAP-aligned, and globally acceptable PDR documentation.

Who We Are

ProdDev is a specialized pharmaceutical development documentation service provider, focused exclusively on:

• PDR Protocol preparation

• PDR Report writing & independent review

• Product development lifecycle & regulatory support

Our Expert Team

• Pharmaceutical formulation scientists

• Regulatory affairs professionals

• QA & GMP experts

• Technical documentation specialists

We bridge the gap between:

• Formulation development → Scale-up → Regulatory approval

• R&D data → Authority-acceptable documentation

• Development stage → Commercial & import readiness

Our Core PDR Services – Pharma (UAE Focused)

📘 Product Development Report (PDR) Documentation

• Complete PDR Protocol preparation

• PDR Report writing with strong scientific justification

• Development rationale for QTPP, CQA, CMA & CPP

• Comparative development & optimization studies

• Excipient selection & compatibility justification

• Scale-up and manufacturing readiness justification

🔍 PDR Review & Gap Assessment

• Independent technical & regulatory review of existing PDRs

• Gap assessment against ICH, CTD & MOHAP expectations

• Risk identification with corrective recommendations

• 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 MOHAP / DHA / DoH development-related 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)

Global Regulatory Alignment

Our PDR documents are prepared in line with:

• ICH Guidelines (Q8, Q9, Q10, Q11)

• CTD / eCTD dossier structure

• WHO Technical Report Series (TRS)

• MOHAP UAE regulatory requirements

• GCC, EU, ASEAN, LATAM & ROW frameworks

This ensures UAE-registered and imported products meet regional and global expectations.

Industries We Serve in the UAE

• Pharmaceutical manufacturers & importers

• Marketing Authorization Holders (MAHs)

• Export-oriented pharma companies

• Contract Development & Manufacturing Organizations (CDMOs)

• Regulatory affairs & compliance consultancies

Why UAE Pharma Companies Choose ProdDev

✅ 600+ PDRs successfully prepared & reviewed
✅ Strong UAE & GCC regulatory experience
✅ MOHAP-aligned, inspection-ready documentation
✅ Integrated R&D, QA & Regulatory expertise
✅ End-to-end product development lifecycle support
✅ Confidential, reliable & deadline-driven execution

Our Structured PDR Approach

1. Product understanding & scope finalization

2. Regulatory & development requirement mapping

3. PDR protocol preparation / review

4. Scientific PDR report writing with backup data

5. Independent QA & regulatory review

6. Submission-ready delivery & authority query support

Who We Work With

We support pharmaceutical clients across:

UAE | GCC | Middle East | Africa | Europe | Asia | LATAM

From local MOHAP submissions to regional GCC and global registrations, our PDRs are designed to be authority-ready and inspection-acceptable.

Confidentiality & Compliance

All projects are handled under strict:

• Confidentiality agreements

• Data integrity principles

• GMP & international regulatory compliance standards

Get in Touch – UAE PDR Specialists

Looking for PDR Protocol & Report preparation, review, or MOHAP regulatory query support for your pharmaceutical product in the UAE?

📩 Contact ProdDev – Product Development Experts
A Scientific Arm of Zoesoe Exports Pvt. Ltd.