ISO 9001 Certification in Saudi Arabia

GMP Certificate Assistance in Saudi Arabia

GMP Certification in Saudi Arabia is more than a compliance checkbox — it’s a strategic assurance of product safety, consistency, and market credibility. As the Kingdom advances Vision 2030, robust GMP (Good Manufacturing Practices) systems help manufacturers protect consumers, reduce operational risk, and unlock regional and global market access. From Riyadh and Jeddah to Dammam and Al Khobar, organizations in pharmaceuticals, nutraceuticals, food & beverages, cosmetics/personal care, and medical devices are adopting GMP to meet SFDA expectations and international buyer requirements.
GMP defines the controls needed to consistently manufacture safe, high-quality products: qualified facilities and equipment, validated processes, hygiene and environmental controls, documented procedures, trained personnel, and full batch traceability. When implemented well, GMP becomes a practical, scalable production system that reduces defects, prevents contamination, and strengthens brand trust.
VerosCert offers GMP Certification Services in Saudi Arabia.We support organizations with a clear, results-driven methodology—from initial gap assessment to documentation, validation, training, internal audits, and final certification/inspection support. Our expert team helps you build a right-sized GMP program aligned with SFDA requirements and recognized international frameworks (e.g., WHO GMP, PIC/S, ISO 22716 for cosmetics, ISO 22000/FSSC 22000 for food safety, and ISO 13485 for medical devices).

GMP Certification Services in Saudi Arabia

gmp Gap Analysis & Awareness Training
Gap Analysis & GMP Awareness

We start with a GMP gap analysis benchmarking your facilities, utilities, processes, and controls against SFDA, WHO/PIC/S, and relevant ISO standards (ISO 22716, ISO 13485, food GMP), followed by awareness sessions on hygiene zoning, ALCOA+ data integrity, documentation discipline, and team roles.

gmp Documentation & Implementation Support
Documentation & GMP Implementation Support

We create/refine SOPs, MBRs, cleaning & sanitation, validation (process/cleaning), change control, deviation/CAPA, complaints/recall, supplier qualification, and training records—tailored to your operations and embedded into daily workflows for a practical, compliant GMP system.

gmp Pre-Audit Review & Internal Assessments
Pre-Inspection Review & Internal Assessments

Before certification/inspection, we run mock inspections and internal audits—line walkthroughs, document sampling, environmental trend reviews, and data-integrity checks—to identify nonconformities, drive CAPA, and ensure readiness for SFDA or third-party audits.

gmp Audit Coordination & Certification Assistance
Audit Coordination & Certification Assistance

VerosCert coordinates with recognized GMP certification bodies and supports you through regulatory inspections (including SFDA). We assist during document reviews and on-site assessments, facilitate auditor communications, and help close observations with effective CAPA—so you achieve a successful GMP outcome.



Turning GMP Principles into Business Impact

At VerosCert, we believe GMP certification is more than compliance — it’s about building a quality-by-design culture that protects consumers, reduces risk, and improves efficiency. By helping teams apply the core GMP principles, we ensure your certification journey delivers lasting business value, not just a certificate.

Customer Focus
01
Hygiene & Contamination Control

Prevent cross-contamination through zoning, sanitation, environmental monitoring, and disciplined personnel hygiene and gowning.

Leadership
02
Documentation & Data Integrity (ALCOA+)

Maintain complete, accurate, contemporaneous records (MBRs, logs, COAs) to ensure traceability, right-first-time release, and inspection readiness.

Engagement of People
03
Qualified Facilities, Utilities & Equipment

Design and qualify HVAC, water, compressed air, and equipment (DQ/IQ/OQ/PQ) with calibrated, well-maintained assets for consistent performance.

Process Approach
04
Process Control, Validation & Risk Management

Validate manufacturing and cleaning processes, define critical parameters and IPCs, and use change control and QRM to keep processes stable and compliant.

Improvement
05
Competent People & Quality Culture

Build capability with role-based training, SOP adherence, line clearance discipline, and leadership that reinforces accountability on the shop floor.

Evidence-Based Decision Making
06
Materials & Supplier Management

Qualify suppliers, control incoming materials, enforce quarantine/release, FEFO, and full batch traceability to protect product integrity.

Relationship Management
07
Deviation, CAPA & Continuous Improvement

Investigate deviations/OOS/OOT, identify root causes, implement effective CAPAs, trend performance, and drive continual improvement via management review.

GMP Certification Cost in Saudi Arabia

GMP certification/inspection costs in Saudi Arabia vary based on your organization’s size, number of sites/lines, product risk class (pharma, food, cosmetics, devices), and the maturity of your current GMP controls. At VerosCert, we offer transparent, competitive pricing for both SMEs and large enterprises—aligned with SFDA expectations and international schemes (WHO/PIC/S, ISO 22716, ISO 13485, ISO 22000). We also provide Vision 2030–friendly SME discounts and bundled packages (e.g., GMP + ISO 22000/ISO 22716/ISO 13485/ISO 9001) for maximum efficiency. Reach out for a no-obligation GMP cost estimate.

  • Preparatory activities like gap analysis and risk assessment
  • Development or revision of documentation
  • Internal training and employee awareness programs
  • Audit Duration and Complexity
  • Certification Body Fees
  • Maintenance and Surveillance Costs

GMP Certification Process

Getting GMP certified in Saudi Arabia is a structured journey focused on building an inspection-ready Good Manufacturing Practice system. At VerosCert, we partner with you end-to-end — from GMP gap analysis and QRM to documentation, facility & utilities readiness, validation, training, and mock inspections — ensuring you meet SFDA, WHO/PIC/S, and relevant ISO expectations with confidence and a culture of continual improvement.

1 st

Submit Enquiry & Define GMP Requirements

2 nd

Conduct Gap Analysis & Identify Gaps

3 rd

Develop Documentation & GMP Framework

4 th

Deliver Awareness Training & Build GMP Culture

5 th

Implement GMP & Conduct Internal Audits

6 th

Coordinate External Audit & Achieve Certification
cta

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GMP Benefits
Benefits of GMP Certification

Why GMP Matters for Saudi Arabia & Vision 2030

Saudi Arabia’s Vision 2030 is reshaping the Kingdom as a global hub for business excellence, innovation, and sustainable development. GMP certification plays a crucial role in helping Saudi manufacturers align with national goals, ensure product safety, and enhance global competitiveness.

  • Strengthens manufacturing controls and fosters a culture of continuous improvement
  • Ensures product safety and consistency to meet SFDA, WHO/PIC/S, and international buyer expectations
  • Enhances competitiveness in both local and export markets
  • Builds investor and partner confidence through traceable, inspection-ready processes
  • Supports regulatory compliance and improves sector-specific performance (pharma, food, cosmetics, devices)
Industries We Serve

GMP Certification Solutions Across Key Sectors

Saudi Arabia stands as one of the most influential economies in the Middle East, powered by world-class energy capabilities, ambitious infrastructure, and a rapidly evolving industrial base. Under the Saudi Vision 2030 framework, the Kingdom is expanding beyond oil into pharmaceuticals & biotech, nutraceuticals, food & beverage, cosmetics & personal care, medical devices, packaging, and cold-chain logistics. In this dynamic environment, GMP (Good Manufacturing Practices) Certification in Saudi Arabia has become essential for businesses seeking to ensure product safety, consistency, and regulatory compliance. As the globally recognized benchmark for manufacturing quality, GMP equips organizations with the controls to prevent contamination, validate processes, enforce data integrity (ALCOA+), and maintain full batch traceability—aligning production with SFDA expectations and international frameworks such as WHO/PIC/S, ISO 22716 (cosmetics), ISO 13485 (medical devices), and food-GMP/FSMS standards. Companies across Riyadh, Jeddah, Dammam, and Al Khobar are adopting GMP to enhance operational discipline, reduce waste and deviations, accelerate product release, and build customer and stakeholder trust at home and in export markets. Aligned with Vision 2030, GMP empowers manufacturers to embed risk-based thinking, robust documentation, validation, and continual improvement across every stage of the product lifecycle. By partnering with experienced consultants like VerosCert, Saudi businesses can implement GMP efficiently, pass inspections confidently, and position themselves as leaders in safety, quality, and sustainable growth—both regionally and globally.

  • Pharmaceutical & Biotech Manufacturers: API plants, sterile injectables, oral solids, liquids/ointments, vaccines, biologics, CMOs/CPOs.
  • Nutraceuticals & Dietary Supplements: vitamins/minerals, herbal formulations, sports nutrition, gummies/softgels, contract supplement makers.
  • Food & Beverage Processing & Packaging: dairy & beverages, meat/poultry, seafood, bakery & confectionery, RTE/RTC, central/cloud kitchens, catering.
  • Cosmetics & Personal Care (ISO 22716): skin & hair care, fragrances, soaps/detergents, sanitizers/disinfectants, aerosols, private-label plants.
  • Medical Devices & IVD (with ISO 13485): sterile/non-sterile devices, disposables, implants, diagnostic kits/reagents, dental products.
  • Primary Packaging & Contact Materials: blister films, bottles/vials, closures, syringes, IV bags, laminates, labels for pharma/food/cosmetics.
  • Cold-Chain & Specialized Processing: contract sterilization (EO/gamma), lyophilization services, aseptic compounding/repack (licensed scope).
  • In-house QC/Production Laboratories: microbiology/chemistry labs for release testing, stability, environmental monitoring with ALCOA+ controls.
  • Third-party/Contract Manufacturers & Packers: toll manufacturing, co-packing, relabeling/repackaging operations.
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