ValiPro – Global Process Validation Protocol & Report Services for Morocco
US FDA | EU GMP | WHO | PIC/S | Morocco MOH / DMP Aligned
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 Kingdom of Morocco and the wider North African & EU-linked markets.
Since 2008, ValiPro has been supporting Indian manufacturers, Morocco-based importers, distributors, and Marketing Authorization Holders (MAHs) with regulatory-compliant, authority-acceptable validation documentation, ensuring smooth Ministry of Health & Social Protection (MOH) / Directorate of Medicines and Pharmacy (DMP) approvals, reduced regulatory observations, and faster market access.
Who We Support – Morocco Market
ValiPro works closely with:
• Moroccan pharmaceutical companies importing products from India
• Indian manufacturers exporting finished formulations, APIs, and intermediates to Morocco
• Marketing Authorization Holders (MAHs) submitting dossiers to Morocco MOH / DMP
• Companies preparing for Moroccan GMP inspections and EU-aligned compliance reviews
• Firms responding to DMP validation-related deficiencies and regulatory queries
• Startups and established manufacturers requiring EU- and Africa-acceptable validation documentation
Our services are designed to bridge Indian GMP practices with Morocco MOH/DMP, EU GMP influence, and international regulatory expectations.
Our Process Validation Services
We provide complete lifecycle support for process validation documentation required for Morocco registrations, variations, renewals, and GMP compliance, including:
• Preparation of Process Validation Protocols
• Preparation of Process Validation Reports
• Independent technical review of existing validation documents
• Morocco MOH / DMP / EU authority query handling (post-submission)
• Gap assessment against Morocco GMP, EU 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
• Morocco-specific and EU-aligned regulatory requirements
Our Experience Supporting Morocco & Global Markets
• 870+ products supported globally
• Active projects across Africa, Europe, Middle East, Asia & LATAM
• Experience covering oral solids, injectables, APIs, semi-solids, liquids, extracts, oils, and chemicals
• Hands-on regulatory exposure with Morocco MOH/DMP, EU Authorities, US FDA, 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
• Morocco MOH / DMP GMP and validation expectations
Industries We Serve – Morocco Submissions
• Pharmaceuticals & Finished Dosage Forms
• Active Pharmaceutical Ingredients (APIs)
• Injectables & Sterile Products
• Cosmetics & Personal Care Products
• Herbal & Natural Products
• Essential Oils & Extracts
• Food & Nutraceutical Ingredients
• Industrial & Specialty Chemicals
Why Morocco-Focused Companies Choose ValiPro
• DMP-aligned, authority-ready validation documentation
• Validation formats accepted across Morocco, EU-linked markets, WHO & PIC/S regions
• Strong expertise in EU-influenced GMP inspections and regulatory query handling
• Reduced DMP observations, approval delays, and rework
• Confidential, professional, and deadline-driven execution
• Deep understanding of Indian manufacturing operations supplying North Africa & EU-linked markets
How to Get Started – Morocco Projects
To initiate a Morocco-focused process validation project, simply share:
• Product and manufacturing process details
• Dosage form and batch size
• Indian manufacturing site information
• Target registration, variation, or inspection timeline
• Existing validation data (if available)
Our team will provide a customized technical scope and commercial proposal, fully aligned with Morocco MOH / DMP requirements.