In the pharmaceutical industry, product quality depends not only on formulation but also on the manufacturing equipment and production processes. A manufacturing system designed in compliance with GMP-WHO and EU GMP requirements enables manufacturers to maintain consistent product quality, minimize the risk of cross-contamination, improve production efficiency, and meet regulatory validation requirements.
Investing in modern pharmaceutical manufacturing equipment not only helps optimize productivity and reduce operating costs but also provides a solid foundation for expanding production capacity, registering new products, and entering international markets with stringent quality standards.
TIN NGHI DAC PHARMACEUTICAL EQUIPMENT CO., LTD. specializes in supplying pharmaceutical manufacturing equipment, providing process engineering solutions, and delivering technology transfer services for pharmaceutical, nutraceutical, and cosmetic manufacturing facilities. Our solutions are carefully selected to help manufacturers build production lines that comply with GMP-WHO, EU GMP, and other internationally recognized quality management standards.
What Is GMP-WHO and EU GMP Compliant Pharmaceutical Manufacturing Equipment?
GMP-WHO (Good Manufacturing Practices – World Health Organization) is a set of Good Manufacturing Practice guidelines issued by the World Health Organization (WHO) to ensure that pharmaceutical products are consistently manufactured and controlled according to established quality standards.
EU GMP (European Union Good Manufacturing Practice) is the GMP regulatory framework established by the European Union. Compared with GMP-WHO, EU GMP places more stringent requirements on quality management, risk assessment, data integrity, computerized systems, record traceability, and process validation.
To comply with these standards, pharmaceutical manufacturing equipment must be designed according to hygienic engineering principles, facilitate validation, and provide precise process control throughout the manufacturing process.
Requirements for Equipment Complying with GMP-WHO and EU GMP
Modern pharmaceutical manufacturing equipment is typically designed to meet the following requirements:
- Constructed from SUS304 or SUS316L stainless steel for all product-contact surfaces.
- Product-contact surfaces are polished to a low surface roughness (typically Ra ≤ 0.8 μm) to minimize material adhesion and reduce the risk of cross-contamination.
- Designed without dead legs, allowing easy disassembly, cleaning, maintenance, and inspection.
- Compatible with or capable of integrating CIP (Clean-in-Place) and SIP (Sterilize-in-Place) systems where applicable.
- Equipped with PLC/HMI control systems for automated operation, recipe management, and accurate process control.
- Provides stable control of critical process parameters such as temperature, pressure, airflow, rotational speed, humidity, and processing time.
- Supplied with complete validation documentation, including DQ, IQ, OQ, and PQ.
- Supports production data management, traceability, and Data Integrity requirements in accordance with EU GMP guidelines.
- Designed to facilitate equipment qualification, process validation, and compliance with pharmaceutical quality management systems.
Pharmaceutical Equipment and Technology Solutions from TIN NGHI DAC
TIN NGHI DAC PHARMACEUTICAL EQUIPMENT CO., LTD. supplies a comprehensive range of pharmaceutical manufacturing equipment and process technology solutions for the pharmaceutical, nutraceutical, and cosmetic industries. Our product portfolio includes laboratory R&D equipment, pilot-scale systems, and full-scale industrial manufacturing equipment designed to meet GMP requirements.
The technology solutions provided by TIN NGHI DAC support a wide range of pharmaceutical manufacturing processes, including:
- Wet Granulation
- Dry Granulation
- Fluid Bed Drying
- Tablet Film Coating
- Sustained-Release Pellet Coating
- Enteric Coating
- Powder Layering
- Pellet Layering
- Hot Melt Granulation
- Spray Granulation
Our equipment is suitable for manufacturing:
- Tablets
- Capsules
- Pellets
- Sustained-Release Pellets
- Enteric-Coated Pellets
- Orally Disintegrating Tablets (ODT)
- Chewable Tablets
- Oral Granules
- Dietary Supplements / Nutraceuticals
- Cosmetic Products
Supporting Manufacturers in Achieving International GMP Compliance
Committed to delivering advanced pharmaceutical manufacturing technologies, TIN NGHI DAC continuously introduces innovative formulation and processing solutions to help manufacturers improve productivity, optimize production efficiency, and enhance product quality.
Our experienced engineering team is ready to assist customers in selecting the most suitable equipment for research, scale-up, commercial production, and the development of manufacturing facilities that comply with GMP-WHO, EU GMP, and other international quality standards, helping pharmaceutical companies strengthen their competitiveness and achieve sustainable growth.
Pharmaceutical Granulation and Drying Equipment
This category of equipment plays a vital role in raw material preparation by producing uniform granules, controlling moisture content, and improving final product quality. TIN NGHI DAC provides advanced solutions for fluid bed granulation, hot melt granulation, spray drying, fluid bed drying, and other modern material processing systems.
Tablet Film Coating Equipment
Film coating equipment is widely used in the production of pharmaceutical tablets and dietary supplements. These systems protect active ingredients, improve product stability, enhance tablet appearance, and increase the commercial value of finished products.
Film Coating Equipment
Hot Melt Extrusion and Pelletizing Equipment
TIN NGHI DAC provides advanced pelletizing solutions for the production of tablets, pellets, and specialized dosage forms. Our equipment is designed to ensure product uniformity, maximize production efficiency, and comply with the stringent manufacturing standards of the pharmaceutical industry.
Hot Melt Extruders & Pelletizers
Milling and Mixing Equipment
To meet demanding requirements for particle size and material homogeneity, we offer ultra-fine milling systems, jet mills, multi-directional mixers, and advanced material processing solutions suitable for a wide range of pharmaceutical ingredients and active compounds.
Milling & Mixing Equipment
Integrated Pharmaceutical Production Line Solutions
In addition to standalone equipment, TIN NGHI DAC provides consulting, engineering, and turnkey pharmaceutical production lines tailored to customers’ specific manufacturing requirements. Our solutions optimize production efficiency while ensuring compliance with current GMP standards.
With an extensive product portfolio and a highly experienced engineering team, TIN NGHI DAC is committed to delivering advanced pharmaceutical equipment solutions that help manufacturers enhance production capacity and improve product quality.
Why Choose GMP-Compliant Equipment from TIN NGHI DAC?
International Quality Standards
All equipment is manufactured in accordance with pharmaceutical industry standards and meets rigorous quality and inspection requirements.
Application-Oriented Engineering Consultation
Our engineering team assists customers in selecting the most appropriate equipment based on:
- Production scale
- Required capacity
- Dosage form
- Investment budget
Comprehensive Installation Support
Our turnkey services include:
- Facility layout design
- Equipment installation
- Commissioning
- Operator training
- Preventive maintenance
Complete Technical Documentation
Customers receive comprehensive documentation, including:
- Product Catalogues
- Engineering Drawings
- Operation Manuals
- IQ/OQ Documentation
- Operating Instructions
Applications Across Multiple Industries
Equipment supplied by TIN NGHI DAC is widely used in:
- Pharmaceutical Manufacturing Plants
- Traditional Herbal Medicine Manufacturers
- Dietary Supplement Manufacturing Facilities
- Cosmetic Manufacturing Plants
- Chemical Processing Plants
- Research Institutes
- Universities
- Quality Control Laboratories
TIN NGHI DAC’s Commitment
We are committed to delivering exceptional quality and customer satisfaction through the following commitments:
- Genuine pharmaceutical manufacturing equipment.
- Pharmaceutical-grade construction materials.
- Competitive pricing.
- Clear warranty policies.
- Prompt technical support.
- Readily available spare parts.
- Long-term partnership and after-sales service.
Read More: Trusted Pharmaceutical Equipment Supplier in Vietnam
Contact Us for Pharmaceutical Manufacturing Equipment Consultation
If your company is looking for GMP-WHO compliant pharmaceutical manufacturing equipment, contact TIN NGHI DAC PHARMACEUTICAL EQUIPMENT CO., LTD. for expert consultation and customized solutions. We supply everything from standalone machines to complete turnkey pharmaceutical production lines, meeting the requirements of modern manufacturing facilities with a commitment to Quality – Efficiency – Sustainability.
Tin Nghi Dac Pharmaceutical Equipment Co., Ltd.
Tax Code: 3703422032
Office phone: (+84)28 66719989
Mobile: (+84)329 280 289
Email: info@xinyite.com.vn
Address: 49C D11 Street, Group 18, Quarter 4, An Phu Ward, Ho Chi Minh City, Vietnam.
