Results 1 to 10 of about 74,235 (210)

Development of the general chapters of the Chinese Pharmacopoeia 2020 edition: A review

open access: yesJournal of Pharmaceutical Analysis, 2021
The Chinese Pharmacopoeia 2020 edition was reviewed and approved by the National Medical Products Administration and the National Health Commission of the People's Republic of China in July 2020. The current edition was officially implemented on December
Zhaopeng Yang
exaly   +3 more sources

Development of chromatographic technologies for the quality control of Traditional Chinese Medicine in the Chinese Pharmacopoeia

open access: yesJournal of Pharmaceutical Analysis, 2021
As an important branch of medicine, Traditional Chinese Medicine (TCM) has been applied for the treatment of diseases for thousands of years in China and other countries in East Asia.
Ming-Rui Shen, Yi He, Shang-Mei Shi
exaly   +3 more sources

Pharmacopoeia roles and responses: A systemic resilience approach to COVID-19 pandemic

open access: yesSaudi Pharmaceutical Journal, 2022
The Coronavirus Disease (COVID-19) is sweeping around the world at a rapid pace resulting in severe health crises across the globe. The pandemic condition has forced the government, regulatory authorities, bio/pharmaceutical industry, and healthcare ...
Shruti Rastogi   +6 more
doaj   +1 more source

Ensuring the quality of medicines in India: An update on the development, modernization, and harmonization of drug standards in the Indian Pharmacopoeia

open access: yesSaudi Pharmaceutical Journal, 2023
India has a sparkling pharmaceutical sector that holds a distinguished place by producing and supplying high-quality and affordable medicines across the globe.
Gaurav Pratap Singh Jadaun   +8 more
doaj   +1 more source

Monitoring of residual solvent contamination in herbal medicinal products in Ghana: A pilot study

open access: yesScientific African, 2021
The use of herbal medicinal products for complementary and alternative medicine is well established in Ghana. The potential public health risks associated with the use of these products due to the presence of residual solvents have not yet been ...
Kwabena F.M. Opuni   +5 more
doaj   +1 more source

Identification of Potent Bioassay Guided Terpenoid and Glycoside Root Fractions of Astragalus candolleanus against Clinically Significant Bacterial Strains

open access: yesInternational Journal of Microbiology, 2022
Antibiotic resistance represents one of the biggest challenges, and there is an urgent need for plant-based antimicrobial agents that enable managing this crisis effectively.
Kandasamy Nagarajan   +9 more
doaj   +1 more source

Public-private partnership (3Ps) in ensuring safe use of medicines: An Indian experience

open access: yesFrontiers in Public Health, 2022
Adverse drug reactions (ADRs) are major concerns to the public health. To monitor ADRs and ensure patients' safety, the Pharmacovigilance Programme of India (PvPI) has been established by the Government of India in 2010.
Vivekanandan Kalaiselvan   +4 more
doaj   +1 more source

Reporting on antibiotic use patterns using the WHO Access, Watch, Reserve classification in the Caribbean

open access: yesRevista Panamericana de Salud Pública, 2022
Objective. To assess antibiotic use in three hospitals in three Caribbean countries based on data from 2013 and 2018 using the World Health Organization Essential Medicines List “Access, Watch, Reserve” (AWaRe) classification. Methods.
Tamarie Rocke   +4 more
doaj   +1 more source

Rupture Test and Bioavailability of Oil-Soluble Vitamins [PDF]

open access: yes, 2013
In lieu of an abstract, here is the article\u27s first paragraph: Bioavailability of multi-vitamins as dietary supplements has always been a concern. Dissolution studies have been successfully used to predict drug release of bioactive molecules, but with
Chablani, Lipika
core   +2 more sources

The Comparative Study of Different Pharmacopoeias: Indian Pharmacopoeia, British Pharmacopoeia, United States Pharmacopoeia

open access: yesOpen Access Journal of Pharmaceutical Research, 2023
The objective of the study is to ensure Indian pharmacopoeia monographs are on par with United States, British pharmacopoeia standards. A few monographs were selected on random and compared. It has been observed that Indian pharmacopoeia has replaced titrimetrry assay method of analysis to sophisticated chromatographic techniques.
openaire   +1 more source

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