Class 1k Gmp Modular Cleanroom Systems Project Wall Material

Product Overview 

Implementing a cleanroom is a strategic investment that delivers measurable returns. It safeguards production yields by drastically reducing contamination-related defects and waste, ensures uncompromising compliance with regulatory standards to avoid costly penalties, and fundamentally protects your brand reputation by guaranteeing product purity and reliability for end-users.

Cleanroom Description

Technical Specifications

Features at a Glance

1. 1. Control Airborne Contaminants: Helps reduce airborne particle contamination through HEPA/ULPA filtration and controlled airflow.

   2. Stabilize the Environment: Precisely regulate critical parameters including temperature, humidity, and pressure to ensure process consistency.

   3. Support Contamination Control: Create a physical and aerodynamic barrier to isolate sensitive processes, protecting both the product and surrounding areas.

   4. Support Controlled Personnel and Material Entry: Mitigate human-borne contamination through stringent protocols for gowning, material entry, cleaning, and personnel behavior.

   5. Support Testing and Validation: Continuously monitor environmental conditions and validate overall performance against stringent industry standards (e.g., ISO, GMP).

Cleanroom Applications

Pharmaceutical & Biotechnology

Modular cleanroom systems can be configured for pharmaceutical and biotechnology applications requiring controlled airborne contamination, environmental conditions and pressure relationships.

Laboratory & R&D

Prefabricated cleanrooms can be adapted for laboratory, testing and research environments according to the required cleanliness classification and process conditions.

Electronics & Semiconductor

Cleanroom configurations can support electronics and precision manufacturing processes where airborne particle and environmental control are important.

Medical & Healthcare

Cleanroom systems can be configured for selected medical, healthcare and controlled production environments according to applicable project requirements.

Relevant Cleanroom Project Experience

Pharmaceutical Cleanroom Project – Mauritius

Location: Mauritius

Industry: Pharmaceutical Manufacturing

Project Type: Turnkey Cleanroom Project

Cleanroom Classification: ISO 7

Scope: Design, HVAC, Installation and Validation

Status: Successfully Delivered

Cleanroom Testing & Validation

Cleanroom performance can be evaluated according to the project requirements through appropriate testing procedures. Depending on the configuration and applicable requirements, testing may include airborne particle counting, airflow velocity, differential pressure, temperature, humidity, illumination, noise and filter integrity testing where applicable.

SHP can support project qualification documentation, including DQ, IQ, OQ and PQ where required.

Integrated Cleanroom System Components

Integrated Cleanroom Systems and Component Supply

SHP delivers an integrated supply scope covering GMP-grade wall panels, cleanroom ceilings, doors, windows and HVAC components, supporting turnkey cleanroom project implementation.

The following image shows the major systems and products commonly integrated into SHP cleanroom projects.

Company Profile

As a leading supplier of clean room system and clean room products,SHP is an organization that prides itself both on technical expertise as well as next level customer care.SHP offers Cleanroom Solutions to meet our clients' particular requirements specialized for pharmaceutical,biotechnology and microelectronic cleanrooms.We also provide a range of Clean Room products including wall panel,door&window and a series of clean room equipment.

As an ISO 9001:2015 certified organization,we are committed to continually improving our customer service programs while meeting or exceeding your product quality criteria.With our comprehensive customer solution offerings,excellence in products,and decades of technical expertise,we are confident that SHP can match the best to your application.

Our Customers

Project Delivery & Export Documentation

Cleanroom Project Material Delivery

The following photos record the packaging, container loading and international shipment of the cleanroom project supplied by SHP.

The shipment included GMP-grade wall panels, cleanroom envelope materials and accessories prepared for overseas installation.

FAQ

1. What is included in the Class 1K GMP modular cleanroom system?

The modular cleanroom system can be configured with prefabricated wall and ceiling panels, cleanroom doors and windows, HEPA filters or FFU units, HVAC equipment, flooring systems, lighting and supporting electrical components. The final equipment and material scope is determined according to the required cleanroom classification, production process, room layout and project requirements.

2. Can SHP customize the cleanroom classification and system configuration?

Yes. SHP can develop a project-specific cleanroom configuration according to the required cleanliness classification, production process, room pressure relationship, temperature and humidity requirements, room layout and applicable standards. The final classification and system parameters are confirmed during the engineering and design stage.

3. How does SHP verify the performance of a completed cleanroom?

SHP can support cleanroom commissioning, testing and validation according to project requirements. Typical verification items may include airborne particle concentration, airflow velocity, differential pressure, temperature, humidity, illumination and noise. Where required, qualification activities can include DQ, IQ, OQ and PQ.

4. Can SHP provide testing and validation documentation for cleanroom projects?

Yes. Testing and validation documentation can be prepared according to the project requirements and applicable procedures. SHP's cleanroom project documentation can include commissioning records, test results and qualification documentation. Third-party testing or verification can also be arranged where required by the project.

5. What information does SHP need to prepare a modular cleanroom quotation?

To prepare a project-specific quotation, SHP normally needs information such as the cleanroom dimensions or available floor area, required cleanliness classification, application or production process, room layout, temperature and humidity requirements, pressure requirements, HVAC requirements and project location. If some information is not yet available, SHP can first review the available project requirements and recommend a suitable configuration.

6. What cleanroom engineering experience does SHP have?

SHP reports more than 20 years of cleanroom engineering experience, with more than 2,100 completed projects and project delivery experience in more than 40 countries. Its engineering services cover cleanroom design, manufacturing, installation, commissioning, testing and validation for pharmaceutical, biotechnology, laboratory, electronics and other controlled-environment applications.