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IPC Holds 2nd GC‑Based EG & DEG Training for State Drug Labs — Enhancing Medicine Safety

The Indian Pharmacopoeia Commission held its second hands‑on training (22‑23 June 2026) on GC‑based detection of ethylene glycol and diethylene glycol in oral liquid medicines. The programme, attended by analysts from six states, supports the IP Amendment List 09 requirement and strengthens state drug testing laboratories to safeguard public health.
Overview The IPC organised its second hands‑on training on the determination of EG and DEG in oral liquid preparations using GC . The two‑day programme ran from 22 June to 23 June 2026 at the IPC campus in Ghaziabad. Key Developments Inaugurated by Dr V. Kalaiselvan, Secretary‑cum‑Scientific Director, IPC , with Shri Rajeev Bhargava, Deputy Drugs Controller, Delhi as Guest of Honour. Participants from six states – Haryana, Goa, Odisha, West Bengal, Assam and Meghalaya – received practical training on sample preparation, instrument calibration, chromatogram interpretation and data analysis. The training aligns with IP Amendment List 09 , which now requires EG and DEG testing in every oral liquid drug. Hands‑on sessions covered the scientific basis of glycol contamination, regulatory requirements, and routine application of GC for compliance. Important Facts EG and DEG are not permitted in any pharmaceutical formulation. They may enter products through adulterated excipients such as glycerin, propylene glycol, sorbitol or polyethylene glycol. Even trace levels can cause acute kidney injury, central nervous system depression and death. The new amendment makes it compulsory for all State Drug Testing Laboratories to incorporate these tests into their routine workflow. UPSC Relevance The episode illustrates how regulatory bodies translate policy into capacity‑building actions. It highlights the role of the IPC in safeguarding public health, a frequent topic in GS 3 (Health, Science & Technology). Understanding the toxicology of EG and DEG, and the analytical method of GC , helps answer questions on drug safety, quality control and regulatory compliance. Way Forward Continued training of analysts across states will ensure uniform implementation of the amendment. The IPC plans to expand similar programmes to cover other high‑risk contaminants. Strengthening laboratory infrastructure, standardising protocols and promoting inter‑state knowledge sharing are essential steps to protect consumers and uphold the integrity of India’s pharmaceutical supply chain.
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Key Insight

IPC training equips state labs to detect deadly glycols, boosting drug safety

Key Facts

  1. IPC organised a two‑day training on EG and DEG detection using gas chromatography on 22‑23 June 2026 at its Ghaziabad campus.
  2. Participants came from six states – Haryana, Goa, Odisha, West Bengal, Assam and Meghalaya.
  3. The programme implements IP Amendment List 09 to the Indian Pharmacopoeia 2022, which mandates EG and DEG testing in all oral liquid medicines.
  4. Ethylene glycol (EG) and diethylene glycol (DEG) are highly toxic; even trace amounts can cause kidney failure and death.
  5. State Drug Testing Laboratories must now include EG and DEG tests in their routine quality‑control workflow.
  6. The event was inaugurated by Dr V. Kalaiselvan, Secretary‑cum‑Scientific Director, IPC, with Shri Rajeev Bhargava, Deputy Drugs Controller, Delhi, as Guest of Honour.

Background

The Indian Pharmacopoeia Commission, a statutory body under the Ministry of Health, sets drug quality standards. By training state lab analysts, it translates the regulatory requirement of Amendment List 09 into practical capacity, linking health governance with scientific quality control.

UPSC Syllabus

  • GS2 — Functions and responsibilities of Union and States
  • Essay — Youth, Health and Welfare
  • Prelims_CSAT — Data Interpretation
  • Prelims_GS — Constitution and Political System

Mains Angle

GS 3 (Health, Science & Technology) – discuss how bodies like IPC ensure drug safety through standards, testing mandates and capacity‑building programmes.

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Overview

Full Article

Overview

The IPC organised its second hands‑on training on the determination of EG and DEG in oral liquid preparations using GC. The two‑day programme ran from 22 June to 23 June 2026 at the IPC campus in Ghaziabad.

Key Developments

  • Inaugurated by Dr V. Kalaiselvan, Secretary‑cum‑Scientific Director, IPC, with Shri Rajeev Bhargava, Deputy Drugs Controller, Delhi as Guest of Honour.
  • Participants from six states – Haryana, Goa, Odisha, West Bengal, Assam and Meghalaya – received practical training on sample preparation, instrument calibration, chromatogram interpretation and data analysis.
  • The training aligns with IP Amendment List 09, which now requires EG and DEG testing in every oral liquid drug.
  • Hands‑on sessions covered the scientific basis of glycol contamination, regulatory requirements, and routine application of GC for compliance.

Important Facts

EG and DEG are not permitted in any pharmaceutical formulation. They may enter products through adulterated excipients such as glycerin, propylene glycol, sorbitol or polyethylene glycol. Even trace levels can cause acute kidney injury, central nervous system depression and death. The new amendment makes it compulsory for all State Drug Testing Laboratories to incorporate these tests into their routine workflow.

Exam Relevance

The episode illustrates how regulatory bodies translate policy into capacity‑building actions. It highlights the role of the IPC in safeguarding public health, a frequent topic in GS 3 (Health, Science & Technology). Understanding the toxicology of EG and DEG, and the analytical method of GC, helps answer questions on drug safety, quality control and regulatory compliance.

Way Forward

Continued training of analysts across states will ensure uniform implementation of the amendment. The IPC plans to expand similar programmes to cover other high‑risk contaminants. Strengthening laboratory infrastructure, standardising protocols and promoting inter‑state knowledge sharing are essential steps to protect consumers and uphold the integrity of India’s pharmaceutical supply chain.

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IPC training equips state labs to detect deadly glycols, boosting drug safety

Key Facts

  1. IPC organised a two‑day training on EG and DEG detection using gas chromatography on 22‑23 June 2026 at its Ghaziabad campus.
  2. Participants came from six states – Haryana, Goa, Odisha, West Bengal, Assam and Meghalaya.
  3. The programme implements IP Amendment List 09 to the Indian Pharmacopoeia 2022, which mandates EG and DEG testing in all oral liquid medicines.
  4. Ethylene glycol (EG) and diethylene glycol (DEG) are highly toxic; even trace amounts can cause kidney failure and death.
  5. State Drug Testing Laboratories must now include EG and DEG tests in their routine quality‑control workflow.
  6. The event was inaugurated by Dr V. Kalaiselvan, Secretary‑cum‑Scientific Director, IPC, with Shri Rajeev Bhargava, Deputy Drugs Controller, Delhi, as Guest of Honour.

Background & Context

The Indian Pharmacopoeia Commission, a statutory body under the Ministry of Health, sets drug quality standards. By training state lab analysts, it translates the regulatory requirement of Amendment List 09 into practical capacity, linking health governance with scientific quality control.

UPSC Syllabus Connections

GS2•Functions and responsibilities of Union and StatesEssay•Youth, Health and WelfarePrelims_CSAT•Data InterpretationPrelims_GS•Constitution and Political System

Mains Answer Angle

GS 3 (Health, Science & Technology) – discuss how bodies like IPC ensure drug safety through standards, testing mandates and capacity‑building programmes.

Analysis

Related PYQs

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Practice Questions

Prelims
Easy
Prelims MCQ

Pharmaceutical toxicology

2 marks
4 keywords
GS3
Medium
Mains Short Answer

Regulatory standards

10 marks
5 keywords
GS3
Hard
Mains Essay

Drug safety and regulatory capacity

20 marks
5 keywords
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IPC Holds 2nd GC‑Based EG & DEG Training f... | UPSC Current Affairs