ValiPro – Global Process Validation Protocol & Report Services for Jordan

US FDA | EU | WHO | PIC/S | Jordan FDA (JFDA) & Country MOH 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 Jordan-based manufacturers supplying to 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 regulatory approvals, reduced inspection observations, and faster access to international markets.

Who We Support in Jordan

ValiPro works closely with:

• Jordanian manufacturers exporting to US, EU, UK, GCC, MENA, Africa & LATAM
• Companies preparing for JFDA, US FDA, EU GMP, WHO & PIC/S inspections
• Firms addressing regulatory deficiencies, observations, and validation queries
• New manufacturing facilities and established plants requiring globally acceptable validation documentation
• Export-oriented manufacturers targeting regulated and semi-regulated markets

Our services are structured to meet Jordan GMP and JFDA requirements 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
• JFDA / FDA / EU / WHO authority query handling (post-submission & inspection response support)
• Gap assessment against Jordan-specific GMP and validation guidelines
• 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
• Jordan manufacturing facility layout and utilities
• Target export market regulatory expectations

Our Experience

• 870+ products supported globally
• Active projects across Middle East, Asia, Africa, Europe & LATAM
• Experience across oral solid dosage forms, injectables, APIs, semi-solids, liquids, herbal extracts, oils, and chemicals
• Direct regulatory exposure with JFDA, US FDA, EU Authorities, WHO, PIC/S & country MOHs
• Proven success in new registrations, variations, revalidation, technology transfer, 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
• Jordan FDA (JFDA) and Ministry of Health expectations

Industries We Serve in Jordan

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

Why Jordanian Companies Choose ValiPro

• Regulatory-focused, authority-ready 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 prepare a customized scope of work and commercial proposal aligned with your Jordan FDA and global regulatory requirements.