Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Behind every facility expansion, technology investment, and quality milestone in the CDMO sector is a leadership team making deliberate choices about where to focus, how to grow, and when to take calculated risks.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
A video roundup of the week’s top industry news stories.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A one-on-one video interview between our editorial teams and industry leaders.
Listen to expert discussions and interviews in pharma and biopharma.
Contract Pharma Stream offers a centralized destination where users can watch expert-led sessions anytime, anywhere
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
It is the first regulatory milestone for the manufacturing facility since it was commissioned in 2020.
July 24, 2026
By: Patrick Lavery
Content Marketing Editor
Editor’s Take: Implementing continuous flow will heighten the company’s operational safety, while also reducing its carbon footprint.
The U.S. FDA conducted a successful, short-notice Pre-Approval Inspection of Asymchem’s carbapenem API manufacturing facility in China in April.
The site, known as Dunhua 2 (DH2, Jilin Asymchem Pharmaceuticals Co.) received notification of the inspection’s success in June. Asymchem says the inspection supported a commercial API using continuous raw material feeding and reaction technology.
More specifically, the DH2 site provides custom carbapenem intermediates to APIs, supporting clinical to commercial supply. On-site are cutting-edge continuous flow ozonolysis capabilities, built in-house.
Capacity reaches into tonnage scale, in support of new chemical entities.
Dating back to when the site was commissioned in 2020, this marks its first regulatory milestone.
Hao Hong, PhD, Chairman and CEO of Asymchem Group, reflected on the significance of the successful inspection. Hong said the U.S. joins the European Union, Japan, China, Australia, Korea, Canada, and Brazil in validating Asymchem facilities.
“This first inspection of Asymchem’s Dunhua 2 facility confirms our unwavering commitment in achieving the highest quality standards,” Hong added.
To that end, Asymchem believes that implementing continuous flow across all its sites prioritizes heightened operational safety. It also, according to the company, will reduce its carbon footprint.
Asymchem, a global CDMO, says it successfully completes approximately 200 customer audits per year across all operations. Additionally, the company’s facilities have completed more than 100 regulatory inspections to date.
Worldwide, Asymchem employs more than 10,000 professionals. The company is committed to a Quality by Design framework that utilizes science- and risk-based approaches, and data-driven decision-making.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !