Evidence map›Paper›PMID 37965488›Full record

ReviewSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society2023

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

Gaurav Pratap Singh Jadaun, Shruti Rastogi, Amit Kumar, Jaishiv Chauhan, Surendra Kumar Sharma, Mukesh Kumar, Pawan Kumar Saini, Ritu Tiwari, Rajeev Singh Raghuvanshi

Abstract readReview
In one paragraph

Review in Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Gaurav Pratap Singh JadaunIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Shruti RastogiIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Amit KumarIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Jaishiv ChauhanIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Surendra Kumar SharmaIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Mukesh KumarIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Pawan Kumar SainiIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Ritu TiwariIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.
Rajeev Singh RaghuvanshiIndian Pharmacopoeia Commission, Ministry of Health and Family Welfare, Government of India, Sector 23, Raj Nagar, Ghaziabad 201 002, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

India has a sparkling pharmaceutical sector that holds a distinguished place by producing and supplying high-quality and affordable medicines across the globe. Ensuring the quality and safety of the marketed medicinal products is one of the most important components of the drug regulatory framework and assessment of the quality of medicines is usually achieved by referring to the public standards of the official Pharmacopoeia. In India, the Indian Pharmacopoeia (IP) is published at regular intervals to fulfill the requirements of the Drugs and Cosmetics Act, 1940 to ensure the quality of medicines being manufactured and/or marketed in India. The present article aims to provide an overview of the history of the IP, its standards-setting process, and the current status of monographs in the 9th edition of the IP 2022. Special focus is placed on the newly added and upgraded general chapters and monographs within the IP 2022. There are a total of 223 general chapters and 3152 drug monographs available under various categories in the IP 2022. This study also highlights a total of 92 new drug monograph additions and 412 monograph revisions in the IP 2022. It is anticipated that the standards laid down in the IP 2022 will play an imperative role in delivering quality medicines to patients within and outside India.

Indexed as

Active pharmaceutical ingredientsFinished pharmaceutical preparationsIndian pharmacopoeiaMonographReference standards

Identifiers

PMID37965488
PMCPMC10641554

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.