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Cleanroom Engineering (ISO 5-8) in Liberia Engineering Excellence & Technical Support

Cleanroom Engineering (ISO 5-8) solutions for Bioprocessing & Manufacturing. High-standard technical execution following OEM protocols and local regulatory frameworks.

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ISO Class 5 Cleanroom Design & Validation

Expert design and validation of ISO Class 5 (Class 100) cleanrooms, ensuring rigorous particulate control for critical pharmaceutical manufacturing and sensitive research applications in Liberia's burgeoning life sciences sector.

ISO Class 7 & 8 Contamination Control Strategies

Implementing advanced HEPA/ULPA filtration, laminar flow systems, and precise airflow management for ISO Class 7 and 8 cleanrooms, safeguarding production integrity in industries like food processing and electronics assembly across Liberia.

HVAC Systems & Environmental Monitoring for ISO Compliance

Specialized design and maintenance of HVAC systems with integrated real-time environmental monitoring (particulate counts, temperature, humidity) to ensure sustained ISO 5-8 compliance and operational excellence in Liberian cleanroom facilities.

What Is Cleanroom Engineering (Iso 5-8) In Liberia?

Cleanroom Engineering, particularly focusing on ISO Class 5 to 8 standards, in Liberia refers to the specialized design, construction, and maintenance of controlled environments that minimize the presence of airborne particulate contamination. These cleanrooms are essential for processes that demand high levels of purity to ensure product integrity, prevent cross-contamination, and maintain regulatory compliance. The core principle is the rigorous control of environmental parameters such as particulate matter, temperature, humidity, pressure differentials, and airflow patterns through advanced HVAC systems, filtration, and material selection.

Who Needs Cleanroom Engineering (ISO 5-8) in Liberia?Typical Use Cases
Pharmaceutical and Biotechnology Companies: For drug manufacturing, sterile product packaging, cell culture, and genetic research where microbial and particulate contamination can render products ineffective or unsafe.Sterile injectable drug production (ISO 5)Aseptic filling and finishing (ISO 5/7)Microbiological testing laboratories (ISO 7/8)API (Active Pharmaceutical Ingredient) manufacturing (ISO 7/8)
Medical Device Manufacturers: To produce devices requiring sterile or highly controlled environments, preventing infections and ensuring device functionality.Surgical instrument manufacturing (ISO 7)Implantable device production (ISO 5/7)Diagnostic kit assembly (ISO 7/8)
Electronics Manufacturers (especially microelectronics): For assembling sensitive electronic components where dust and particles can cause short circuits or product failure.Semiconductor fabrication (historically higher classes, but relevant for specialized processes)Assembly of sensitive electronic components (ISO 7/8)Printed circuit board (PCB) manufacturing and assembly (ISO 7/8)
Food and Beverage Industry: For processing and packaging of certain sensitive food products to ensure safety and prevent spoilage.Dairy product processing (e.g., infant formula) (ISO 7/8)Specialty food ingredient manufacturing (ISO 7/8)
Research and Development Laboratories: Across various scientific disciplines requiring controlled environments for experiments.General laboratory research (ISO 8)Specialized analytical testing (ISO 7/8)

Key Aspects of Cleanroom Engineering (ISO 5-8) in Liberia:

  • Design and Construction: Involves architectural planning, selection of appropriate materials (e.g., non-shedding surfaces, antistatic components), and integration of specialized air handling units (AHUs), HEPA/ULPA filtration systems, and monitoring equipment.
  • Validation and Certification: A crucial step to confirm that the cleanroom meets the specified ISO standard through rigorous testing and documentation. This includes air particle counting, airflow velocity measurements, pressure difference verification, and filter integrity testing.
  • Operational Protocols and Training: Establishment of strict operational procedures for personnel gowning, material transfer, cleaning, and general behavior within the cleanroom to maintain contamination control.
  • Maintenance and Monitoring: Ongoing surveillance of environmental parameters and regular maintenance of filtration systems, HVAC equipment, and seals to ensure continued compliance with the defined ISO class.
  • Decontamination and Sterilization: Application of appropriate cleaning and sterilization techniques for the specific cleanroom application and industry sector.

Who Needs Cleanroom Engineering (Iso 5-8) In Liberia?

Cleanroom engineering, particularly for ISO 5 to ISO 8 standards, is crucial for industries requiring highly controlled environments to prevent contamination. While Liberia's industrial landscape is developing, specific sectors and emerging areas can significantly benefit from these advanced cleanroom capabilities. This ensures product integrity, research accuracy, and safety in critical processes.

Industry/SectorSpecific Departments/ApplicationsReason for Cleanroom Requirement (ISO 5-8)
Pharmaceutical Manufacturing & PackagingActive Pharmaceutical Ingredient (API) synthesis, sterile product filling, sterile filtration, packaging of sensitive drugsPrevent airborne particulate contamination, microbial contamination, and cross-contamination to ensure drug efficacy, safety, and sterility. ISO 5 for sterile filling, ISO 7/8 for packaging and general manufacturing.
Medical Device ProductionSterile implant manufacturing, assembly of sensitive diagnostic equipment, sterilization processesEliminate particulate and microbial contamination that could lead to patient infections, device failure, or inaccurate readings. ISO 5 for critical assembly, ISO 7/8 for less critical stages.
Research & Development Laboratories (Biotech, Academia)Cell culture, molecular biology, genetic engineering, microbiology, advanced materials researchMaintain sterile conditions for sensitive biological experiments, prevent contamination of cell lines, ensure the integrity of genetic material, and achieve reproducible research results. ISO 5 for sterile cell culture, ISO 7/8 for general lab work.
Electronics Manufacturing (Emerging)Assembly of sensitive electronic components, microchip fabrication (potential future development)Prevent static discharge and particulate contamination that can damage delicate electronic components, leading to device malfunction or reduced lifespan. ISO 6/7 often sufficient for general assembly, ISO 5 for highly sensitive processes.
Food & Beverage Processing (High-Purity)Production of infant formula, sterile dairy products, specialized nutritional supplementsPrevent microbial contamination and spoilage, ensuring product safety and extending shelf life. ISO 7/8 for production areas, ISO 5 for critical filling or packaging steps.
Cosmetics & Personal Care ProductionManufacturing of sterile creams, lotions, and eye care productsMinimize microbial contamination and prevent the introduction of impurities that could affect product safety and efficacy. ISO 7/8 for production, ISO 5 for specific filling or formulation steps.

Target Customers and Departments for Cleanroom Engineering (ISO 5-8) in Liberia

  • Pharmaceutical Manufacturing & Packaging
  • Medical Device Production
  • Research & Development Laboratories (Biotech, Academia)
  • Electronics Manufacturing (Emerging)
  • Food & Beverage Processing (High-Purity)
  • Cosmetics & Personal Care Production

Cleanroom Engineering (Iso 5-8) Process In Liberia

Cleanroom engineering processes, particularly for ISO 5-8 classifications, involve a structured workflow from initial client inquiry to successful execution and validation. This workflow ensures that the designed and constructed cleanroom meets stringent contamination control standards, crucial for industries like pharmaceuticals, biotechnology, and advanced manufacturing. The process is iterative and requires close collaboration between the client, the engineering firm, and potentially regulatory bodies.

StageDescriptionKey ActivitiesDeliverablesTimeframe (Indicative)
  1. Inquiry and Needs Assessment
Initial contact from the client to discuss their cleanroom requirements and objectives.Understanding client's application, industry standards (ISO 5-8), process flow, personnel flow, material flow, contamination risks, and budget. Site assessment (if applicable).Project brief, initial proposal, scope of work definition.1-2 Weeks
  1. Conceptual Design and Feasibility Study
Developing preliminary designs and evaluating the feasibility of the project based on the defined requirements.Defining cleanroom classification, size, layout, air change rates, filtration strategies (HEPA/ULPA), HVAC system concepts, pressure differentials, material of construction, and utility requirements. Cost estimation.Conceptual drawings, preliminary layout, basic system schematics, initial cost estimate, feasibility report.2-4 Weeks
  1. Detailed Design and Engineering
Producing comprehensive engineering drawings, specifications, and documentation for construction.Developing detailed HVAC design (ductwork, diffusers, fans), electrical design (lighting, power distribution, controls), plumbing, instrumentation, architectural drawings (walls, doors, windows, flooring), material specifications, and BIM modeling (if used).Detailed engineering drawings (mechanical, electrical, architectural), Bill of Materials (BOM), technical specifications, equipment datasheets, project schedule.4-12 Weeks
  1. Procurement and Manufacturing
Sourcing and fabricating all necessary components and equipment.Tendering and selecting suppliers/manufacturers. Ordering specialized cleanroom components (airlocks, pass-boxes, cleanroom panels, filters). Manufacturing custom-built equipment.Procured materials and equipment, manufactured components.8-20 Weeks (overlaps with Design & Construction)
  1. Construction and Installation
On-site assembly and installation of the cleanroom infrastructure and systems.Site preparation, installation of structural elements, HVAC system installation (ductwork, AHUs), electrical wiring, lighting, flooring, wall/ceiling systems, doors, windows, and utilities. Careful adherence to cleanroom construction protocols.Installed cleanroom structure and systems.12-30 Weeks
  1. Commissioning and Qualification
Testing and verifying that all systems function as designed and meet specifications.Pre-functional checks, functional performance testing (air balancing, airflow patterns, pressure differentials, temperature/humidity control), static and dynamic testing. Preparation of IQ/OQ protocols.Commissioning reports, functional test results, initial data for qualification.4-8 Weeks
  1. Validation and Certification
Formal verification that the cleanroom meets the specified ISO classification and operational requirements.Installation Qualification (IQ): Verifying correct installation of all equipment. Operational Qualification (OQ): Verifying systems operate within defined parameters. Performance Qualification (PQ): Verifying the cleanroom maintains the required ISO class under normal operating conditions. Particle counting, microbial monitoring, airflow visualization.IQ, OQ, PQ reports, cleanroom certification certificate.2-4 Weeks
  1. Handover and Training
Transferring ownership and providing necessary training to the client's personnel.As-built drawings, O&M manuals, spare parts list. Training on cleanroom operation, maintenance, cleaning protocols, and emergency procedures.Completed handover documentation, trained personnel.1 Week
  1. Post-Execution Support and Maintenance
Ongoing support to ensure continued performance and compliance.Scheduled maintenance, filter replacement, recalibration of instruments, troubleshooting, and periodic recertification as per regulatory requirements.Maintenance logs, recertification reports.Ongoing

Cleanroom Engineering (ISO 5-8) Process in Liberia: Workflow Breakdown

  • Inquiry and Needs Assessment
  • Conceptual Design and Feasibility Study
  • Detailed Design and Engineering
  • Procurement and Manufacturing
  • Construction and Installation
  • Commissioning and Qualification
  • Validation and Certification
  • Handover and Training
  • Post-Execution Support and Maintenance

Cleanroom Engineering (Iso 5-8) Cost In Liberia

Cleanroom engineering projects in Liberia, particularly for ISO 5 to ISO 8 classifications, can involve significant investment. The cost is heavily influenced by a multitude of factors, making it crucial for businesses to conduct thorough feasibility studies and obtain detailed quotes. These classifications represent increasingly stringent levels of particle control, with ISO 5 (Class 100) being the most demanding. The specific requirements for ventilation, filtration, materials, monitoring, and construction methods will directly impact the overall price.

Several key pricing factors contribute to the total cost:

  • ISO Classification: As mentioned, a lower ISO number (e.g., ISO 5) signifies a higher level of cleanroom performance, requiring more advanced and expensive technology, stricter construction, and more rigorous testing, thus increasing costs significantly compared to higher ISO classifications (e.g., ISO 8).
  • Size and Layout: The overall footprint and complexity of the cleanroom design (e.g., number of rooms, corridors, airlocks) will naturally dictate material and labor expenses.
  • Materials and Finishes: The selection of flooring, wall panels, ceiling tiles, doors, and windows is critical. Materials must be non-shedding, easy to clean, and resistant to disinfectants, often leading to higher-grade, specialized products.
  • HVAC System Design: The sophisticated airflow management, HEPA/ULPA filtration, pressure differentials, and air change rates required for cleanrooms are a major cost driver. This includes the cost of specialized air handling units, ductwork, and filtration systems.
  • Lighting and Electrical Systems: Cleanroom lighting is often integrated into the ceiling and must meet specific lumen output and color rendering index requirements, while electrical systems need to be designed to prevent particle generation.
  • Ancillary Equipment: This can include pass boxes, gowning rooms, specialized sinks, waste disposal systems, and air showers, all of which add to the project's expense.
  • Instrumentation and Monitoring: Continuous monitoring of particle counts, temperature, humidity, and pressure is essential for validation and ongoing operation. The cost of sophisticated monitoring equipment and sensors can be substantial.
  • Installation and Labor: Skilled labor with experience in cleanroom construction is crucial. The cost of specialized technicians, electricians, and general construction workers in Liberia will influence the pricing.
  • Design and Engineering Fees: Professional services for designing the cleanroom layout, HVAC systems, and ensuring compliance with relevant standards are a necessary upfront cost.
  • Validation and Commissioning: Rigorous testing and certification by accredited third-party agencies are required to ensure the cleanroom meets its intended ISO classification. This is a critical, non-negotiable expense.
  • Location and Site Preparation: Accessibility to the construction site, potential need for site modifications, and logistical challenges in Liberia can affect costs.
  • Project Management: Effective oversight and management of the entire construction process are vital for staying on budget and schedule.

Pricing Ranges (Estimated in Liberian Dollar - LRD):

Due to the specialized nature of cleanroom construction and the current economic landscape in Liberia, precise, universally applicable pricing is challenging to provide. Costs are highly project-specific. However, based on global averages and considering potential local factors, the following estimated ranges for cleanroom engineering (ISO 5-8) in Liberia can be considered. It is imperative to obtain detailed, site-specific quotes from experienced cleanroom construction companies.

Cleanroom ClassificationEstimated Cost Range (per sq meter in LRD)Notes
ISO 8 (Class 100,000)1,500,000 - 3,500,000 LRDLower end for basic configurations, higher end for more advanced features and larger spaces.
ISO 7 (Class 10,000)2,500,000 - 5,500,000 LRDRequires more sophisticated HVAC and materials than ISO 8.
ISO 6 (Class 1,000)4,000,000 - 8,000,000 LRDSignificant increase in HVAC efficiency, filtration, and construction precision.
ISO 5 (Class 100)7,000,000 - 15,000,000+ LRDThe most stringent and expensive classification, requiring highly advanced systems, materials, and rigorous validation. Costs can escalate rapidly for specialized applications.

Key Pricing Factors for Cleanroom Engineering (ISO 5-8) in Liberia

  • ISO Classification Level (ISO 5, 6, 7, 8)
  • Cleanroom Size (Square Meters/Footage)
  • Room Layout and Complexity (Number of Rooms, Airlocks)
  • High-Performance HVAC System (Air Changes per Hour, Filtration - HEPA/ULPA)
  • Specialized Construction Materials (Wall panels, flooring, ceilings, doors, windows)
  • Gowning Rooms and Pass-Through Chambers
  • Air Showers and Downflow Booths
  • Environmental Monitoring Systems (Particle counters, sensors)
  • Lighting and Electrical Systems Design
  • Design and Engineering Services
  • Installation Labor and Supervision
  • Validation, Testing, and Certification
  • Ancillary Equipment and Utilities
  • Project Management and Logistics
  • Site-Specific Requirements and Preparations

Affordable Cleanroom Engineering (Iso 5-8) Options

Achieving ISO 5-8 cleanroom standards can be a significant investment. This guide explores affordable engineering options, focusing on value bundles and cost-saving strategies to make cleanroom compliance more accessible. We'll break down typical project components and offer practical advice for optimizing your budget without compromising essential performance.

Value Bundle ComponentDescriptionCost-Saving StrategyEstimated Cost Range (Relative)
Basic ISO 7/8 EnclosureStandard HEPA filtration, basic wall panels (e.g., melamine or pre-finished metal), PVC flooring, basic lighting.Opt for standard materials, fewer doors/airlocks, simpler HVAC integration.$ (Lower)
Enhanced ISO 7/8 with Laminar FlowIncludes features of the basic bundle plus localized laminar flow modules for critical zones, higher-grade wall panels (e.g., coved cove base), reinforced flooring.Targeted laminar flow zones instead of full room, consider modular laminar flow units.$$ (Moderate)
Certified ISO 5/6 CoreHigh-efficiency HEPA/ULPA filtration, multi-stage air handling, advanced sealing techniques, stainless steel or specialized resin flooring, robust lighting, sophisticated control systems.Focus on essential clean zones, minimize the area requiring the highest ISO class, explore energy-efficient air handlers.$$$ (Higher)
Integrated HVAC & FiltrationCustom-designed air handling units (AHUs) with integrated filtration, precise temperature and humidity control.Standardized AHU components, optimize ductwork size, explore VFDs (Variable Frequency Drives) for energy savings.Part of all bundles, cost scales with complexity.
Installation & CommissioningProfessional installation of all components, rigorous testing, and certification to ISO standards.Minimize site disruption, pre-fabrication where possible, clear project management.Part of all bundles, can vary significantly based on complexity and location.

Key Considerations for Affordable Cleanroom Engineering

  • Understanding Your Specific Needs: Precisely defining your ISO class, airflow requirements, contamination control targets, and operational processes is crucial to avoid over-engineering and unnecessary costs.
  • Phased Approach to Construction: Consider building your cleanroom in phases if your budget is limited. Start with the essential ISO class and expand functionality or higher cleanliness levels later.
  • Material Selection: Choosing cost-effective yet compliant materials is vital. Explore different filter types, wall panel systems, and flooring options that balance performance with price.
  • Modular vs. Stick-Built: Modular cleanrooms often offer faster installation and predictable costs, while stick-built can provide more customization. Evaluate which approach best suits your project timeline and budget.
  • Leveraging Existing Infrastructure: If possible, integrate your cleanroom into existing building structures to reduce the need for complete new construction.
  • Smart Airflow Management: Optimizing fan selection, ductwork design, and filter placement can reduce energy consumption and operational costs.
  • Experienced, Focused Design: Working with engineers who specialize in cost-effective cleanroom design can prevent costly mistakes and ensure efficient resource allocation.

Verified Providers In Liberia

Finding reliable and qualified healthcare providers is paramount for individuals seeking quality medical care in Liberia. Franance Health stands out as a leading credentialing body, rigorously vetting medical professionals to ensure they meet the highest standards of competence, ethics, and patient care. This dedication to verification not only safeguards patients but also builds trust and confidence in the Liberian healthcare system.

Provider TypeFranance Health Verification Key IndicatorsBenefits for Patients
Doctors (Specialists & General Practitioners)Medical School Accreditation, Board Certification, Residency Completion, Peer Reviews, Continuing Medical Education (CME) RecordsAccurate diagnoses, effective treatment plans, specialized care for complex conditions, reduced risk of medical errors.
Nurses (RNs, LPNs, etc.)Nursing School Accreditation, Licensure Exams, Clinical Competency Assessments, Criminal Background ChecksSafe administration of medications, skilled patient monitoring, compassionate care, adherence to nursing protocols.
DentistsDental School Accreditation, Licensure, Specialization Certifications, Infection Control ProtocolsOral health expertise, pain management, preventive dental care, restorative and cosmetic procedures.
PharmacistsPharmacy School Accreditation, Licensure, Drug Dispensing Accuracy Audits, Continuing Education on TherapeuticsAccurate prescription fulfillment, medication counseling, drug interaction checks, safe storage and handling of pharmaceuticals.
Therapists (Physical, Occupational, etc.)Degree in Relevant Field, Licensure, Clinical Experience, Rehabilitation SpecializationsEffective rehabilitation programs, pain reduction, improved mobility and function, enhanced quality of life.

Why Franance Health Credentials Represent the Best Choice:

  • Rigorous Vetting Process: Franance Health employs a comprehensive evaluation of medical education, licensure, clinical experience, and professional conduct.
  • Commitment to Patient Safety: Their credentialing process prioritizes patient well-being and ensures providers are equipped to deliver safe and effective care.
  • Upholding Ethical Standards: Franance Health verifies that providers adhere to the highest ethical principles and professional codes of conduct.
  • Promoting Excellence in Healthcare: By identifying and endorsing qualified professionals, they contribute to the overall improvement of healthcare services in Liberia.
  • Enhanced Patient Trust: Patients can be confident that a Franance Health-credentialed provider has met stringent quality benchmarks.
  • Facilitating Access to Quality Care: Their work helps streamline the process for patients to find trustworthy healthcare professionals.
  • Continuous Monitoring and Re-evaluation: The credentialing process often involves ongoing assessment to ensure continued adherence to standards.

Scope Of Work For Cleanroom Engineering (Iso 5-8)

This Scope of Work outlines the engineering services for the design, validation, and commissioning of cleanroom facilities adhering to ISO 5, ISO 6, ISO 7, and ISO 8 classifications. The project encompasses all necessary technical deliverables and will be executed in accordance with relevant industry standards and specifications.

DeliverableDescriptionStandard Specification / Reference
Cleanroom Design ReportDetailed documentation of the cleanroom layout, airflow strategies, filtration systems, material selection, and GAMP 5 compliance.ISO 14644-1, ISO 14644-4, ISO 14644-5, GAMP 5
HVAC System DesignDesign of HEPA/ULPA filtration, air handling units (AHUs), ductwork, diffusers, controls for temperature, humidity, pressure differentials, and air change rates.ASHRAE 52.2, ISO 14644-2, SMACNA HVAC Duct Construction Standards
Electrical System DesignDesign of power distribution, lighting (including UV germicidal options), grounding, emergency power, and instrumentation wiring.NFPA 70 (NEC), IEC 60364 Series, ISO 14644-2
Plumbing and Process Piping DesignDesign of ultrapure water (UPW) systems, process gases, waste drainage, and material transfer systems.ASME B31.3, SEMI Standards (e.g., SEMI PV30, SEMI F47), ISPE Baseline® Pharmaceutical Engineering Guide
Architectural and Structural DesignDesign of cleanroom walls, ceilings, floors, doors, windows, pass-throughs, and material suitable for cleanroom environments.ISO 14644-1, ISO 14644-4, GMP Guidelines
Automation and Control System DesignDesign of Building Management System (BMS) or dedicated cleanroom control system for monitoring and control of environmental parameters.ISA S88, ISA S95, IEC 61131-3
Validation Master Plan (VMP)Outline of the overall validation strategy, including IQ, OQ, and PQ protocols.ISPE Baseline® Pharmaceutical Engineering Guide, FDA 21 CFR Part 11, EU GMP Annex 1
Installation Qualification (IQ) Protocol & ReportVerification that the cleanroom systems and equipment are installed according to the design specifications.ISPE Baseline® Pharmaceutical Engineering Guide, ISO 14644-2
Operational Qualification (OQ) Protocol & ReportVerification that the cleanroom systems operate as intended within defined limits.ISPE Baseline® Pharmaceutical Engineering Guide, ISO 14644-2
Performance Qualification (PQ) Protocol & ReportVerification that the cleanroom consistently meets its intended use and specified cleanroom classifications under operational conditions.ISPE Baseline® Pharmaceutical Engineering Guide, ISO 14644-2
Airflow and Pressure Differential MeasurementsVerification of unidirectional or turbulent airflow patterns and required pressure differentials between cleanroom zones.ISO 14644-1, ISO 14644-2, ISO 14644-3
Particle Count TestingDetermination of airborne particulate matter concentration to confirm ISO cleanroom classification.ISO 14644-1, ISO 14644-3
HEPA/ULPA Filter Integrity TestingTesting to ensure HEPA/ULPA filters are properly sealed and leak-free.ISO 14644-3, IEST RP-CC001
Temperature and Humidity MappingVerification of uniform temperature and humidity distribution throughout the cleanroom.ISO 14644-2
Room Differential Pressure Monitoring and ControlEnsuring proper pressure gradients are maintained between adjacent areas.ISO 14644-2
Final Project Documentation and HandoverComprehensive package including as-built drawings, O&M manuals, test reports, and training materials.Project-Specific Requirements, ISO 14644-2

Key Project Phases and Activities

  • Conceptual Design and Feasibility Study
  • Detailed Engineering Design (HVAC, Electrical, Plumbing, Architectural, Controls)
  • Procurement and Supply Chain Management
  • Installation and Construction Management
  • Commissioning and Qualification (IQ, OQ, PQ)
  • Training and Handover
  • Project Management and Documentation

Service Level Agreement For Cleanroom Engineering (Iso 5-8)

This Service Level Agreement (SLA) outlines the guaranteed response times and uptime for the provided cleanroom engineering services, specifically for ISO Class 5 to ISO Class 8 environments. This agreement ensures the continuous and optimal functioning of your critical cleanroom operations.

Service CategoryResponse Time Guarantee (Business Hours)Uptime Guarantee (%)Service Level Objective (SLO)
Routine Maintenance & Calibration48 hours99.5%Scheduled to minimize disruption, all scheduled maintenance completed on time.
Emergency Repair (Non-Critical Component Failure)24 hours99.0%Technician dispatched within 24 hours; resolution target within 72 hours.
Emergency Repair (Critical Component Failure - e.g., Air Handler, Primary Filtration)8 hours98.5%Technician dispatched within 8 business hours; resolution target within 48 hours to restore critical function.
Performance Verification & ValidationAs per Project ScheduleN/AAll testing performed according to agreed-upon schedules and standards.
Design & Installation Support48 hours for inquiriesN/APrompt responses to design queries and site support requests during installation phases.

Scope of Services Covered

  • Design, installation, and commissioning of ISO Class 5-8 cleanrooms.
  • Routine maintenance and calibration of HVAC, filtration (HEPA/ULPA), and environmental monitoring systems.
  • Emergency repair services for critical cleanroom components (e.g., air handlers, filters, control systems).
  • Performance verification and validation testing.
  • System upgrades and retrofits.
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