ValiPro – Global Process Validation Protocol & Report Services for Lebanon

US FDA | EU | WHO | PIC/S | Lebanon MoPH 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 Services for Lebanon-based manufacturers supplying to regulated and semi-regulated global markets.

Since 2008, ValiPro has been supporting pharmaceutical, API, cosmetic, herbal, food, and chemical manufacturers with regulatory-compliant, authority-acceptable process validation documentation, helping ensure smooth approvals, reduced regulatory observations, and faster international market access.

Who We Support in Lebanon

ValiPro works closely with:

• Lebanese manufacturers exporting to EU, US, UK, GCC, MENA, Africa & LATAM
• Companies preparing for Lebanese MoPH, EU GMP, WHO & PIC/S inspections
• Firms responding to regulatory deficiencies, inspection observations, and validation queries
• New manufacturing facilities and established plants requiring globally acceptable validation documentation
• Export-oriented manufacturers seeking compliance with multiple international authorities

Our services are structured to meet Lebanese GMP and MoPH expectations while remaining fully aligned with international regulatory standards.

Our Process Validation Services

We provide complete lifecycle support for process validation documentation, including:

• Preparation of Process Validation Protocols
• Preparation of Process Validation Reports
• Independent technical review of existing validation documentation
• MoPH / FDA / EU / WHO authority query handling (post-submission & inspection support)
• Gap assessment against Lebanon-specific GMP and validation requirements
• Supply of ready-to-use, regulator-accepted validation templates

Each validation document is custom-developed (not generic) and tailored based on:

• Product category and dosage form
• Manufacturing process, equipment, and batch size
• Lebanese facility design, utilities, and operations
• Target export market regulatory expectations

Our Experience

• 870+ products supported globally
• Active projects across Middle East, Asia, Africa, Europe & LATAM
• Experience across oral solids, injectables, APIs, semi-solids, liquids, herbal extracts, oils, and chemicals
• Direct regulatory exposure with Lebanon MoPH, EU Authorities, WHO, PIC/S & US FDA
• Proven success in new registrations, variations, revalidation, and renewals

Regulatory Standards Followed

Our 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 & Validation Requirements
• Lebanese Ministry of Public Health (MoPH) expectations

Industries We Serve in Lebanon

• Pharmaceutical Finished Dosage Forms
• Active Pharmaceutical Ingredients (APIs)
• Cosmetics & Personal Care Products
• Herbal, Traditional & Natural Products
• Food & Nutraceutical Ingredients
• Industrial & Specialty Chemicals

Why Lebanese Companies Choose ValiPro

• Authority-ready, inspection-focused documentation
• Validation formats accepted across multiple export markets
• Strong expertise in inspection readiness and regulatory query response
• Reduced regulatory observations and rework
• Confidential, professional, and deadline-driven execution
• Deep understanding of regional manufacturing and export challenges

How to Get Started

To initiate a validation project, simply share:

• Product and process details
• Dosage form and batch size
• Target export countries
• Submission or inspection timeline
• Existing validation data (if available)

Our technical team will provide a customized technical scope and commercial proposal aligned with Lebanon MoPH and international regulatory requirements.