Hedinger Premium Pharmaceutical Excipients | CPHI China 2026, Booth E3F08 – We Look Forward to Welcoming You

From June 16 to 18, 2026, CPHI & PMEC China will take place at the Shanghai New International Expo Centre, spanning a massive exhibition area of 240,000 square meters. With over 20 years of continuous development, CPHI & PMEC China has significantly expanded its scale and influence, now recognized as one of the leading benchmarks for the pharmaceutical industry across Asia and the world.

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 Floor Plan

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 Booth Preview

In the biopharmaceutical field, pharmaceutical excipients are key components for formulation processing and therapeutic efficacy, directly affecting drug stability, dissolution behavior, and bioavailability. In generic drug consistency evaluation and innovative formulation development, high-quality excipients serve as the cornerstone for precise drug release and robust manufacturing processes.

At this year’s CPHI, Gencloud, in partnership with Hedinger – a century-old European excipient supplier – will present a range of excipient products that comply with multiple pharmacopoeias, GMP standards, and high specifications at Booth E3F08. Below are some of our star products:

m-Cresol

Registration No.: F20170000422 | Status: Active (A)
Manufactured in full compliance with GMP standards and meets Chinese, European, and U.S. pharmacopoeia specifications. Features extremely low endotoxin and impurity levels.

Glycerol (for injection)

Registration No.: F20180000411 | Status: Active (A)
Fully synthetic glycerol, free from biological-source proteins and amino acids. Manufactured in full compliance with GMP standards and meets Chinese, European, and U.S. pharmacopoeia specifications. Offers extremely low microbial and endotoxin levels, as well as very low aldehyde and ketone content.

Propylene Glycol (for injection)

Registration No.: F20190000146 | Status: Active (A)
Manufactured in full compliance with GMP standards and meets Chinese, European, and U.S. pharmacopoeia specifications. Features extremely low endotoxin levels, commercial-scale production capacity, and consistent batch-to-batch stability.

Isopropyl Alcohol

Manufactured in full compliance with GMP standards and meets European, U.S., and Japanese pharmacopoeia specifications, as well as the EU Biocidal Products Regulation. Available in customized concentrations, diluted with purified water compliant with European Pharmacopoeia standards.

If you would like to learn more product details or request our catalog, please feel free to contact us. We also welcome you to visit our booth during the exhibition for face-to-face conversations.

Scan the QR code below to complete visitor registration before 00:00 (midnight) on June 12, 2026, and receive a complimentary on-site ticket (valued at RMB 100). This exhibition adopts a pre-show “online real-name advance registration” system and on-site verification of “physical ID cards.” Please be sure to bring your original ID card for entry.