Home
About Us
Brand Story
Honors
Product Certifications
RICH-TEK Advantage
RICH-TEK Services
Consultancy & Design
Detailed Secondary Design & Construction
Validation Services
RICH-TEK Products
Service Cases
Food & Nutraceuticals
Pharmaceutical & Bio-industry
Electronics & Semiconductors
Healthcare & Medical Industry
Machining & Fabrication
Blog
Latest News
Industry Insights
Join Us
Talent Philosophy
Personnel Notice
Contact Us
中
Outlook and Preparations for Our Company’s Participation in the CPHI Shanghai Pharmaceutical Exhibition in 2025
2026-02-06 16:21
In 2025, our company will participate in the CPHI Pharmaceutical Exhibition held in Shanghai, a premier global event for the pharmaceutical industry. The exhibition will provide us with an opportunity to showcase our latest products and technologies, while also serving as a platform for collaboration and knowledge exchange with peers across the sector. We will highlight innovative drugs, cutting-edge pharmaceutical equipment, and related services, aiming to expand our market presence and strengthen our brand visibility through this participation.
CCTV "Craftsman Spirit" Exclusive Interview
2026-02-03 09:16
In 2017, Chairman Wei Jinlong granted an exclusive interview to China Central Television.
RICH-TEK participated in the ACHEMA exhibition, held in Frankfurt, Germany, from June 11 to 15, 2018.
2018-06-16 10:43
RICH-TEK participated in the CPHI exhibition in Shanghai, China, from June 20 to 22, 2018.
2018-06-24 10:44
RICH-TEK participated in the CPHI exhibition in Shanghai, China, from June 18 to 20, 2019.
2019-06-22 10:45
RICH-TEK participated in the Pharmtech & Ingredients Exhibition in Moscow, Russia, from November 19 to 22, 2019.
2019-11-25 10:45
What are the standards for GMP cleanrooms?
2022-06-28 11:51
GMP‑compliant cleanrooms are designed to eliminate potential biological activity, dust, and contaminants, thereby fundamentally preventing any factors that could compromise the production of high‑quality products. Consequently, such cleanrooms must adhere to relevant design requirements to ensure that product quality meets regulatory standards. I. Design of the Cleanroom Structure in GMP Facilities 1. Each production stage should be seamlessly connected and facilitate effective hygiene control throughout the process, minimizing the risk of cross‑contamination. 2. In terms of layout, the sequence of processing steps must follow the product’s manufacturing flow, ensuring a smooth transition from less‑clean to more‑clean stages; cross‑contamination and backflow within the process are strictly prohibited. 3. Within the GMP cleanroom…
Functions and Characteristics of GMP Cleanrooms
2022-06-30 16:09
As consumers’ demands for product quality continue to rise, the pharmaceutical industry and related sectors are actively striving to meet the standardized Good Manufacturing Practice (GMP) requirements. A key focus of GMP—both domestically and internationally—is maintaining a sterile, dust‑free production environment, namely GMP‑compliant cleanrooms. At present, GMP‑compliant cleanrooms have become widespread throughout China, and pharmaceutical companies adopt a cautious approach when designing and constructing such facilities. However, existing national standards do not provide specific guidance on the selection of equipment and materials in cleanroom design. For reasons of cost and technical constraints, construction firms often err on the side of conservatism and lag behind best practices, resulting in many newly built or retrofitted…
