ValiPro – Global Process Validation Protocol & Report Services for the UAE
US FDA | EU GMP | WHO | PIC/S | UAE MOHAP Compliant
ValiPro is a specialized scientific arm of Zoesoe Exports Pvt Ltd, providing end-to-end Process Validation Protocol and Process Validation Report preparation, review, and regulatory support services for products supplied to the United Arab Emirates (UAE) market.
Since 2008, ValiPro has been supporting Indian manufacturers, UAE-based pharmaceutical companies, importers, distributors, and Marketing Authorization Holders (MAHs) with regulatory-compliant, authority-acceptable validation documentation, ensuring smooth UAE Ministry of Health & Prevention (MOHAP) approvals, reduced regulatory observations, and faster market access across the UAE and GCC.
Who We Support – UAE Market
ValiPro works closely with:
• UAE pharmaceutical companies importing products from India
• Indian manufacturers exporting finished formulations, APIs, and intermediates to the UAE
• Marketing Authorization Holders (MAHs) submitting dossiers to UAE MOHAP
• Companies preparing for UAE GMP inspections and compliance audits
• Firms responding to MOHAP validation-related deficiencies and regulatory queries
• Startups and established manufacturers requiring GCC-acceptable validation documentation
Our services are designed to bridge Indian GMP practices with UAE MOHAP, GCC, and international regulatory expectations.
Our Process Validation Services
We provide complete lifecycle support for process validation documentation required for UAE MOHAP submissions and GMP compliance, including:
• Preparation of Process Validation Protocols
• Preparation of Process Validation Reports
• Independent technical review of existing validation documents
• MOHAP / US FDA / EU authority query handling (post-submission)
• Gap assessment against UAE GMP, PIC/S, WHO, and ICH guidelines
• Supply of ready-to-use, regulator-accepted validation templates
Each document is custom-developed (not generic) and tailored based on:
• Product category and dosage form
• Manufacturing process, controls, and batch size
• Indian manufacturing facility setup
• UAE MOHAP and GCC-specific regulatory requirements
Our Experience Supporting UAE & Global Markets
• 870+ products supported globally
• Active projects across Asia, Middle East, Africa, Europe & LATAM
• Experience covering oral solids, injectables, APIs, semi-solids, liquids, extracts, oils, and chemicals
• Hands-on regulatory exposure with UAE MOHAP, US FDA, EU Authorities, WHO, PIC/S & country MOHs
• Proven success in new registrations, variations, revalidation, and renewals
Regulatory Standards Followed
ValiPro’s process validation documentation aligns with:
• ICH Q8, Q9, Q10
• WHO Technical Report Series (TRS)
• US FDA Process Validation Guidance
• EU GMP Guidelines & Annexes
• PIC/S GMP Requirements
• UAE MOHAP & GCC GMP expectations
Industries We Serve – UAE Submissions
• Pharmaceuticals & Finished Dosage Forms
• Active Pharmaceutical Ingredients (APIs)
• Injectables & Sterile Products
• Cosmetics & Personal Care Products
• Herbal, Traditional & Natural Products
• Essential Oils & Extracts
• Food & Nutraceutical Ingredients
• Industrial & Specialty Chemicals
Why UAE-Focused Companies Choose ValiPro
• MOHAP-aligned, authority-ready validation documentation
• Validation formats accepted across UAE, GCC, US, EU, WHO & PIC/S markets
• Strong expertise in GMP inspection readiness and regulatory query handling
• Reduced MOHAP observations, approval delays, and rework
• Confidential, professional, and deadline-driven execution
• Deep understanding of Indian manufacturing operations supplying the UAE
How to Get Started – UAE Projects
To initiate a UAE-focused process validation project, simply share:
• Product and manufacturing process details
• Dosage form and batch size
• Indian manufacturing site information
• Target submission or inspection timeline
• Existing validation data (if available)
Our team will provide a customized technical scope and commercial proposal, fully aligned with UAE MOHAP requirements.