Viafarma Solutions

13/09/2026

13/09/2026

Planning a product variation in the UAE? 🇦🇪

Before submitting changes to your registered product, make sure your Marketing Authorization is valid and your regulatory status is up to date.

Changes to artwork, packaging, manufacturing information, specifications, or other registered product details may require regulatory approval.

ViaFarma Solutions can support you with:

✓ Product variations
✓ Renewals
✓ Artwork & label compliance
✓ Regulatory lifecycle management
✓ UAE market entry & registration support

Plan ahead. Stay compliant. Avoid unnecessary delays.

📧 [email protected]
📱 052 818 8358
🌐 viafarma360.com

ViaFarma — Path to Excellence

PharmaceuticalIndustry MarketAccess RegulatoryCompliance UAEBusiness

12/09/2026

Don’t Let Your UAE Registration Expire 🇦🇪

Your product is registered in the UAE — but is the registration still valid?

Marketing authorization is not the end of the regulatory journey. Products must remain compliant through renewals, approved variations, updated documentation and post-marketing requirements.

For pharmaceutical and biological products, the Emirates Drug Establishment currently lists the renewal service at 5 working days, with AED 100 application + AED 3,500 renewal fee. EDE also requires supporting documentation including a valid manufacturing-site registration and pharmacovigilance requirements.

ViaFarma can support your UAE portfolio with:

✓ Marketing authorization renewals
✓ Variations & regulatory updates
✓ Documentation review
✓ Artwork and labeling updates
✓ Post-registration regulatory support

Keep your products compliant and market-ready.

📩 [email protected]
📞 052 818 8358

ViaFarma — Path to Excellence

10/09/2026

🇦🇪
لا تنسَ التجديد.

الحصول على التسجيل ليس نهاية الرحلة التنظيمية.

للحفاظ على منتجاتك متوافقة وجاهزة للاستمرار في السوق، تقدم ViaFarma الدعم في:

✓ تجديد تسجيل المنتجات
✓ التغييرات والتحديثات التنظيمية
✓ مراجعة الوثائق
✓ تحديث ومراجعة العبوات والملصقات
✓ الدعم التنظيمي بعد التسجيل

حافظ على تسجيل منتجاتك محدثًا وعلى استمراريتها في السوق.

📩 [email protected]
📞 052 818 8358

ViaFarma — Path to Excellence

الإمارات RegulatoryAffairs

10/09/2026

ViaFarma can support your UAE portfolio with:

✓ Marketing authorization renewals
✓ Variations & regulatory updates
✓ Documentation review
✓ Artwork and labeling updates
✓ Post-registration regulatory support

Keep your products compliant and market-ready.

📩 [email protected]
📞 052 818 8358

ViaFarma — Path to Excellence

Variations PharmaceuticalRegistration UAEMarket

09/09/2026

Ready to launch your medical device in the UAE? 🇦🇪

ViaFarma Solutions supports medical device companies through the UAE regulatory journey — from initial assessment to EDE registration and market entry.

✓ Regulatory assessment
✓ Documentation support
✓ EDE registration
✓ Market-entry support

Planning to enter the UAE market? Contact us to discuss your product.

📩 [email protected]
📞 052 818 8358

ViaFarma — Path to Excellence

UAEMarketEntry HealthcareUAE

07/09/2026

eCTD Solutions for Pharmaceutical Companies

ViaFarma provides flexible eCTD solutions tailored to your regulatory needs:

💻 eCTD Software Installation
For companies that want to prepare and manage eCTD submissions internally.

📁 eCTD Publishing – Per Dossier
Conversion of CTD or paper dossiers into submission-ready eCTD format, including validation and publishing. Preparation and conversion CTD file and Paper file to eCTD 2025_251014_094522.pdf

Choose the solution that fits your business — without unnecessary investment.

📩 Request a quotation:
[email protected]
📞 052 818 8358

ViaFarma – Path to Excellence

07/09/2026

💻 حلول eCTD لشركات ومصانع الأدوية

تقدم ViaFarma Solutions بالتعاون مع
Dr. Walid Samadi – Pharm Consulting Group ME
حلولاً متكاملة لتجهيز وتقديم الملفات بصيغة eCTD.

يمكنكم اختيار الحل الأنسب لاحتياجاتكم:

🔹 تركيب نظام eCTD Software
للشركات الراغبة في إدارة وتجهيز ملفات eCTD داخلياً.

أو

🔹 eCTD Publishing – Per Dossier
نقوم بتجهيز وتحويل ملفكم CTD / Paper Dossier إلى eCTD، مع الـ Validation وتجهيزه للتقديم للجهة التنظيمية.

خدمة مناسبة لشركات الأدوية، المصانع، وأصحاب ملفات التسجيل الراغبين بحل احترافي دون الحاجة لشراء النظام.

📩 تواصلوا معنا للحصول على عرض سعر:
[email protected]
📱 052 818 8358

ViaFarma Solutions × Pharm Consulting Group ME
Regulatory Solutions for the Pharmaceutical Industry