ValiPro – Global Process Validation Protocol & Report Services for Benin

US FDA | EU GMP | WHO | PIC/S | Benin MOH / ANSM 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 Republic of Benin and the wider West African market.

Since 2008, ValiPro has been supporting Indian manufacturers, Benin-based importers, distributors, NGOs, and Marketing Authorization Holders (MAHs) with regulatory-compliant, authority-acceptable validation documentation, ensuring smooth Ministry of Health (MOH) / ANSM-Benin approvals, reduced regulatory observations, and faster market access.

Who We Support – Benin Market

ValiPro works closely with:

Benin pharmaceutical importers and distributors sourcing from India
Indian manufacturers exporting finished formulations and APIs to Benin
Marketing Authorization Holders (MAHs) submitting dossiers to Benin MOH / ANSM
Companies supporting public tenders, donor-funded and NGO supply programs
Firms responding to MOH / WHO pre-qualification and validation-related queries
Startups and established manufacturers requiring Africa-acceptable validation documentation

Our services are designed to align Indian GMP practices with Benin MOH, WHO, and regional African regulatory expectations.

Our Process Validation Services

We provide complete lifecycle support for process validation documentation required for Benin registrations, renewals, and inspections, including:

• Preparation of Process Validation Protocols
• Preparation of Process Validation Reports
• Independent technical review of existing validation documents
Benin MOH / WHO authority query handling (post-submission)
Gap assessment against WHO TRS, PIC/S, and African MOH GMP 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
Benin-specific and WHO-aligned regulatory requirements

Our Experience Supporting Benin & African Markets

870+ products supported globally
• Active projects across Africa, Asia, Middle East, Europe & LATAM
• Experience covering oral solids, injectables, APIs, semi-solids, liquids, extracts, oils, and chemicals
• Hands-on regulatory exposure with African MOHs, WHO, PIC/S, US FDA & EU Authorities
• 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
Benin Ministry of Health (MOH) and regional African regulatory expectations

Industries We Serve – Benin 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 Benin-Focused Companies Choose ValiPro

MOH-aligned, authority-ready validation documentation
• Validation formats accepted across Benin, West Africa, WHO & PIC/S markets
• Strong expertise in WHO-aligned GMP and tender-based regulatory submissions
• Reduced MOH observations, approval delays, and rework
• Confidential, professional, and deadline-driven execution
• Deep understanding of Indian manufacturing operations supplying Africa

How to Get Started – Benin Projects

To initiate a Benin-focused process validation project, simply share:

• Product and manufacturing process details
• Dosage form and batch size
• Indian manufacturing site information
• Target registration, tender, or inspection timeline
• Existing validation data (if available)

Our team will provide a customized technical scope and commercial proposal, fully aligned with Benin MOH and WHO requirements.