Six red and yellow medicine capsules on a white background
Six red and yellow medicine capsules on a white background

Chinese Pharmacopoeia Reference Standards and Reagents

Produce high quality medicines meeting the standards of the PPRC

Labmix24 offers an extensive range of primary reference standards as well as reagents appropriate for pharmacopoeia analysis in compliance with Chinese Pharmacopoeia (ChP) requirements. These are the official reference substances from the Chinese Pharmacopoeia.

Explore our range of Chinese Pharmacopoeia compendial standards and reagents:

Need support finding Chinese Pharmacopoeia reference standards? Call or e-mail us today:  +49 2852 96064 00 or info@labmix24.com


FAQs | Chinese Pharmacopoeia Standards:

A new batch has been released. Does that mean that the old batch can no longer be used?
How can I check the validity periods of Chinese Pharmacopoeia Pharmaceutical Standard Substances?
Where can I view the specification sheets of the reference materials?

About the Chinese Pharmacopoeia

The Chinese Pharmacopoeia (Pharmacopoeia of the People's Republic of China, PPRC) is the official compendium of drugs of the People's Republic of China and a core component of China's national drug standards. It covers standards of purity, description, tests, dosage, precautions, storage and strength for each drug, and is legally binding for drug R&D, manufacture, import, distribution, use and supervision in China.

The current ChP, in its twelfth edition (2025 Edition), was promulgated jointly by the National Medical Products Administration (NMPA) and the National Health Commission on 25 March 2025 and came into force on 1 October 2025. It is published in Chinese; official English editions are also issued (the official English translation of the 2025 Edition has not yet been released — the 2020 Edition remains the latest official English version).

The ChP 2025 is divided into four volumes containing a total of 6,385 monographs (159 newly added, 1,101 revised and 32 no longer included compared with the 2020 Edition):

Volume I: Traditional Chinese Medicine (3069 monographs)

  • Volume II: Chemical Medicine (2776 monographs)

  • Volume III: Biologics (153 monographs)

  • Volume IV (General Technical Requirements, Guidelines and Pharmaceutical Excipients): 410 general technical requirements, 72 guidelines, 387 monographs of pharmaceutical excipients