GMP

Cleanroom buyers must distinguish between facility compliance (GMP), quality management (ISO 9001), airborne cleanliness classification (ISO 14644), filter efficiency (EN 1822), and equipment safety (CE); no single “cleanroom certification” covers everything, and verifying each standard separately prevents procurement errors and regulatory failures.    1. ISO 9001: Quality Management System Certification  ISO 9001 is a generic quality management system (QMS) standard that evaluates a company’s internal administrative and manufacturing processes. * What it guarantees: It proves that the manufacturer has systematic processes in place for document control, customer satisfaction, design planning, raw material sourcing, and continuous improvement. It ensures that the manufacturer can consistently produce items to their specified standards. * What it does NOT guarantee: ISO 9001 does not specify the physical performance, leak resistance, or filtration efficiency of individual filters. A manufacturer can have an excellent ISO 9001 quality management system but still produce low-efficiency filters if their technical design or equipment is outdated.    2. GMP: Good Manufacturing Practice  GMP (Good Manufacturing Practice) is a regulatory standard that governs the manufacturing of pharmaceuticals, medical devices, biotechnology products, and food items. * What it covers: GMP applies strictly to the end-user’s production process and facility, not to the cleanroom equipment supplier’s factory. GMP is concerned with hygiene, cross-contamination prevention, batch records, validation, and sanitation. * The Supplier’s Role: A cleanroom equipment manufacturer cannot be “GMP-certified” because GMP does not issue certificates to equipment manufacturers. Instead, a cleanroom supplier must be an ISO 9001 GMP cleanroom supplier, meaning they design and build equipment (such as Pass Boxes, Air Showers, and FFUs) that allows the pharmaceutical buyer to comply with GMP regulations (e.g., using easy-to-clean SUS304 surfaces, non-porous seals, and high-efficiency filters).    3. ISO 14644: Cleanroom Airborne Cleanliness Classification  ISO 14644 is a set of international standards specifically written for cleanrooms and associated controlled environments. * What it covers: Specifically, ISO 14644-1 classifies cleanroom cleanliness based on the concentration of airborne particles per cubic meter of air, ranging from ISO Class 1 (cleanest) to ISO Class 9 (least clean). * Supplier vs. Facility: This standard applies to the assembled cleanroom environment in operation, not to individual equipment bought from a catalog. However, equipment like KLC’s Fan Filter Units (FFU) are engineered to meet specific ISO 14644 performance levels when installed in a modular cleanroom grid.    4. CE Marking: Product Safety Compliance  The CE mark is a mandatory conformity marking for products placed on the market within the European Economic Area (EEA). * What it covers: It evaluates mechanical safety, electrical safety, electromagnetic compatibility (EMC), and low-voltage limits for powered cleanroom hardware (such as Fan Filter Units, Air Showers, and laminar flow hoods). It does not evaluate filtration efficiency, but guarantees that the electrical components are safe and will not cause fires or electrical interference.    5. EN 1822 / ISO 29463: HEPA/ULPA Filter Testing Standards  EN 1822 is the definitive European standard for high-efficiency particulate air (HEPA) and ultra-low penetration air (ULPA) filters, now aligned with the global ISO 29463 standard. * What it covers: It certifies the performance of the filter itself. It requires testing the filter’s efficiency at its Most Penetrating Particle Size (MPPS) and guarantees that the filter meets the H13, H14, U15, or U16 rating. This is the single most critical technical certification for high-efficiency filters.      Data Comparison Table: Cleanroom Certifications and Standards  Certification / Standard Primary Issuing / Auditing Body Scope of Evaluation Who Must Have It? How to Verify Authenticity ISO 9001 Accredited registrar (e.g., SGS, TUV, DQS) under IAF Manufacturer’s internal administrative and production QMS Direct physical efficiency of the HEPA/ULPA filter at MPPS Search certificate number on IAF CertSearch or the registrar’s portal GMP Guidelines National food and drug administrations (e.g., FDA, NMPA) Process compliance, hygiene, validation of the end product The pharmaceutical or food processing facility operator Verified via official FDA/NMPA audit reports and site inspections ISO 14644-1 Qualified third-party cleanroom testing agency Airborne particle concentration in the operating cleanroom The physical cleanroom facility (operational status) Review particle counter calibration and physical testing reports CE Marking Certified EU Notified Bodies or Self-Declaration Electrical, electromagnetic, and mechanical machinery safety Manufacturers of powered equipment (FFUs, Air Showers) exported to EU Request the CE Declaration of Conformity (DoC) and test reports EN 1822 / ISO 29463 Certified filtration testing laboratories Direct physical efficiency of the HEPA/ULPA filter at MPPS Every individual HEPA filter used in critical cleanrooms Review the individual DOP/PAO leak-test report and serial number scan    How to Verify Cleanroom Manufacturer Certifications  To protect your facility from substandard equipment, use this systematic approach to verify supplier claims: Check IAF CertSearch for ISO 9001: Do not accept a PDF certificate as absolute proof. Visit the International Accreditation Forum (IAF) database and enter the manufacturer’s name or certificate number to verify its active status, scope of registration, and expiry date. Request Individual EN 1822 Scan Reports: A Tier 1 supplier will provide an individual, serialized test report for every single HEPA filter delivered, showing the exact pressure drop and efficiency measured during a DOP/PAO test scan. If a supplier only provides a “general catalog certificate” or a statistical batch report, do not accept the shipment for critical cleanrooms. Verify CE Testing Scope: For Fan Filter Units (FFUs) and Air Showers, request the actual test reports supporting the CE certificate. Ensure the testing was done by an accredited testing house and includes the Machinery Directive (2006/42/EC) and Low Voltage Directive (2014/35/EU).    KLC Compliance Standards  KLC (Guangzhou KLC Cleantech) is an established, fully certified ISO 9001 GMP cleanroom supplier. Operating a state-of-the-art facility in Guangzhou, China, KLC aligns all manufacturing processes with ISO 9001 quality management guidelines. KLC designs cleanroom equipment, including FFU, Pass Boxes, and Air Showers, specifically to meet global GMP and ISO 14644-1 cleanroom classifications. Additionally, every single HEPA filter produced by KLC is tested and scanned using advanced automatic testing rigs in strict accordance with the EN 1822 standard, with individual test reports provided to clients to support their internal facility validation processes.    FAQ: Cleanroom Certifications  Can a HEPA filter supplier be “GMP certified”? No. GMP (Good Manufacturing Practice) is a regulatory standard that applies to the manufacturer of the final product (such as pharmaceuticals or medical devices), not to the components or suppliers of cleanroom equipment. A HEPA filter supplier can only be certified to ISO 9001, while their filters must comply with the EN 1822 standard. The supplier’s role is to provide compliant, high-quality hardware that enables the end-user’s facility to pass its GMP audits. What is the difference between ISO 14644-1 and EN 1822? ISO 14644-1 defines the classification of cleanrooms based on airborne particle concentrations in the room’s air. EN 1822, on the other hand, is a specific test standard for the air filters installed in those rooms. Simply put, ISO 14644-1 measures the cleanliness of the room as a whole, while EN 1822 measures the technical performance and particle separation efficiency of the HEPA/ULPA filter before it is installed. How do I verify if an ISO 9001 certificate is still active and valid? To verify an ISO 9001 certificate, locate the certificate number, the registrar’s name (e.g., SGS, TUV), and the accreditation body logo (e.g., UKAS, CNAS, ANAB). Next, search the manufacturer’s credentials on the International Accreditation Forum’s database (IAF CertSearch) or directly on the issuing registrar’s website. If the supplier’s name does not appear or if the status is “suspended” or “expired,” the certification is invalid. What does the CE mark cover on an FFU (Fan Filter Unit)? For a Fan Filter Unit (FFU), the CE mark certifies that the unit complies with European safety, health, and environmental protection requirements. This covers electromagnetic compatibility (ensuring the FFU does not interfere with other medical or cleanroom electronics), electrical low-voltage safety (preventing shocks and fire hazards), and mechanical safety of the fan blade assemblies. It does not certify the filtration efficiency of the built-in HEPA filter. What is MPPS in EN 1822, and why is it critical for cleanroom certification? MPPS stands for “Most Penetrating Particle Size,” which is the particle size (typically between 0.1 and 0.25 microns) that a filter has the hardest time capturing. EN 1822 requires testing filters at this specific MPPS. This is critical because if a HEPA filter is certified to capture 99.99% of particles at its MPPS, its efficiency for all other particle sizes (both larger and smaller) will be even higher, ensuring comprehensive cleanroom protection. Does ISO 14644 apply to both laminar and turbulent cleanrooms? Yes, ISO 14644-1 applies to all cleanrooms, regardless of their airflow pattern (laminar unidirectional, turbulent non-unidirectional, or mixed). The standard specifies particle concentration limits per cubic meter of air across nine classes. However, the physical placement and quantity of testing points during qualification will differ depending on the laminar or turbulent airflow design of the cleanroom. What documentation should accompany an H14 HEPA filter delivery? An H14 HEPA filter delivery should always be accompanied by a serialized, individual factory inspection report (DOP/PAO test certificate), an instruction manual, and certificates of material compliance. The individual test report must contain the filter’s serial number (matching the label on the filter frame), the measured airflow volume, the initial pressure drop, and the local and overall filtration efficiency at MPPS. Can a non-certified manufacturer produce cleanroom-compliant equipment? While it is technically possible for a manufacturer without ISO 9001 to build a cleanroom-compliant piece of hardware, it is highly risky for buyers. Without a certified quality management system, there is no guarantee of product consistency, material traceability, or testing integrity. Most cleanroom validation auditors will reject equipment that cannot be backed up by certified manufacturing records and verified testing documentation.    Conclusion  Navigating cleanroom certifications requires verifying separate standards for manufacturing quality, product safety, and filtration efficiency. When selecting hardware, ensure that your supplier’s certifications are valid and active on global registry systems. For assistance with cleanroom equipment compliance and to request certified technical documentation for your upcoming project, visit KLC International at https://www.klcintl.com/.

The core functions and detailed differences between air shower and pass box in cleanrooms: The core commonality of both is to control contamination and maintain the cleanroom environment level. Both must comply with regulations and standards such as GMP and ISO 14644. However, there are significant differences in their applicable objects, working principles, and operating requirements, as detailed below:      I. Similarities  1. Structural Anti-Cross-Contamination Both are equipped with a double-door interlocking device, preventing both doors from opening simultaneously. This physically blocks the direct airflow between the cleanroom and non-cleanroom (or different levels of cleanrooms), preventing cleanroom pressure imbalance and pollutant diffusion.     2. Consistent Regulations and Management Requirements Both must be included in the cleanroom equipment management system, with complete maintenance and calibration records, and subject to regular audits and inspections.Daily cleaning requires the use of lint-free cleanroom wipes to wipe the inner walls, and no miscellaneous items are allowed to be stored inside the equipment to prevent them from becoming new sources of contamination.   3. Similar Maintenance and Calibration Principles Both require regular inspection of the door seal integrity and the operating status of functional components, and timely replacement of aging consumables (such as filters and UV lamps) to ensure that the equipment is always in a compliant operating state.    II. Differences  1. Applicable Objects Air shower are applicable to personnel and large material carriers, such as operators and inspectors entering the cleanroom, as well as stainless steel trolleys and large turnover boxes carrying materials. They can meet the needs of large and bulk material carriers. Pass box are only suitable for small materials, tools, and documents, such as sample bottles, reagent tubes, cleanroom wipes, sterile gloves, and clean versions of batch production records. Personnel or large items are strictly prohibited from passing through.   2. Core Purification Principles The air shower chamber uses high-speed airflow blowing and filtration as its core principle.A fan blows air, filtered by a high-efficiency particulate air (HEPA) filter, through nozzles at a speed of no less than 25 m/s, forcibly removing dust particles and microorganisms attached to personnel clothing fibers and trolley surfaces. The blown-off contaminants are collected through the return air vents and filtered again, forming a circulating purification process. The pass box uses physical isolation and auxiliary disinfection as its core principle. The basic model only achieves spatial isolation through interlocking doors and has no active purification function; models with UV disinfection have a built-in 253.7nm wavelength UV lamp, which, when activated, irradiates for 15-30 minutes, killing bacteria by destroying the DNA structure of microorganisms.There is no airflow blowing function throughout the process, so it does not change the attachment state of particles on the surface of objects.   3. Installation Location and Environmental Requirements The air shower chamber should be installed in the buffer zone at the main entrance for personnel/materials in the clean area, forming a three-level separation between the non-clean area and the clean area (non-clean area → air shower chamber → clean area). The installation area needs to have sufficient space for passage to ensure that the doors can be fully opened. It also needs to be linked to the pressure difference of the clean area; the pressure difference inside the air shower chamber should be slightly lower than the clean area and higher than the non-clean area. The pass box is directly embedded in the partition wall between the clean area and the non-clean area, or between different levels of clean areas. The installation location should be convenient for personnel on both sides to operate. The wall opening size needs to match the specifications of the pass box. No additional pressure difference control is required; it only needs to ensure consistency with the environmental parameters of the surrounding area.   4. Operating Procedure The operating procedure of the air shower chamber is as follows: After personnel or a trolley enters, the outer door closes, and the interlocking device locks the inner door; the infrared sensor triggers the fan to blow air, with a preset blowing time of 15-30 seconds (adjustable according to the cleanroom class); after the blowing is completed, the fan stops, the inner door unlocks, and personnel or the trolley can enter the clean area. Forcibly opening the interlocking doors is prohibited throughout the process. The emergency stop button should only be used in emergency situations. The pass box operates as follows: personnel on the non-clean side open the outer door, place the items inside, and close the outer door to ensure the interlock is activated; if it is a model with UV disinfection, the UV lamp must be turned on and remain on for the set disinfection time before being turned off; personnel on the clean side confirm that the outer door is closed, then open the inner door to retrieve the items, and finally close the inner door. Note that it is prohibited to open either door while the UV lamp is on to prevent UV radiation leakage and potential injury.   5. Maintenance and Calibration Details Daily maintenance of the air shower room includes checking that the fan is running without abnormal noise, the sensing device is sensitive, and the interlock function is working correctly; weekly maintenance includes cleaning the pre-filters, wiping the nozzles, and checking that the door seals are not damaged; monthly maintenance includes checking the integrity of the HEPA filter (PAO leak test) and calibrating the airflow speed to be no less than 25 m/s; every six months, the pre-filters should be replaced and the fan motor should be inspected.   Daily maintenance of the transfer window includes checking that the interlock function is working correctly, the UV lamp indicator light is on (for models with disinfection), and the observation window is free of stains; weekly maintenance includes wiping the internal surfaces with 75% ethanol and checking that the door hinges rotate smoothly; monthly maintenance includes calibrating the UV lamp irradiation intensity (which must reach a bactericidal threshold of ≥70 μW/cm²) and replacing aging seals; quarterly maintenance includes replacing the UV lamp tubes (which typically have a lifespan of 8000 hours).    III. Complementary Functions  The air shower room addresses the active purification of personnel and large material carriers, preventing the entry of large amounts of contaminants into the clean area; the transfer window addresses the sterile isolation and transfer of small items, avoiding disruption of the clean area pressure difference and environmental stability due to frequent door openings. Both are indispensable and together constitute a comprehensive pollution control system for personnel and material entry and exit in the clean area.