Centre reorganises CDSCO Zone Baddi amid Drug Quality Concerns

Baddi:  Amid rising concerns over drug quality and repeated regulatory red flags, the Centre has moved to tighten oversight in Baddi—one of India’s largest pharmaceutical manufacturing hubs—by restructuring the Central Drugs Standard Control Organisation (CDSCO), India’s apex health regulatory agency, in the region.

In an order dated February 27, 2026, CDSCO has decided to reorganise Baddi into three separate sub-zones in view of the “vast geographical spread, large number of regulated establishments, and operational constraints”. Baddi houses a dense cluster of pharmaceutical and formulation units that supply medicines across India and for export and has in recent years faced scrutiny following multiple instances of substandard drug findings by domestic and overseas regulators.

The move comes as the government steps up inspections and enforcement measures, including Risk-Based Inspections (RBI) across manufacturing clusters, after a spate of quality failures.

Under the new structure, the Baddi Zone has been split into Baddi-I Sub-Zone, Baddi-II Sub-Zone, and Chandigarh Sub-Zone, each to be headed by an assistant drugs controller (ADC).

Baddi and the larger Baddi-Barotiwala-Nalagarh (BBN) industrial area are known as one of the country’s largest pharmaceutical manufacturing clusters, with industry estimates suggesting that around a thousand formulation and bulk drug units operate in the region. The belt hosts a mix of major pharmaceutical companies as well as smaller contract and third-party manufacturers, supplying medicines to domestic and export markets.

With the reorganisation, each ADC heading a sub-zone will function independently for regulatory and enforcement activities within their assigned jurisdiction. This includes planning and conducting inspections, investigations, and other regulatory actions in accordance with existing rules and guidelines.

The order states that the ADC(I)s “shall function independently in respect of all day-to-day regulatory and enforcement activities within their assigned jurisdictions”, including “planning and conduct of inspections, investigations and other related regulatory actions”.

Consequent to the restructuring, the Deputy Drugs Controller (India), Baddi Zone, will now perform coordination functions across the three sub-zones rather than directly handling all enforcement activities. The DDC will be responsible for driving the execution of recommended actions arising out of risk-based inspections or corrective action and preventive action (CAPA) and other audit observations, along with operationalising the new CDSCO office building at Baddi. The officer will be responsible for coordinating and facilitating National Regulatory Authority (NRA) assessment for drugs, particularly in respect of vaccines and regulatory systems.

Related Posts

Zydus Lifesciences Q4FY26 net profit rises 9%

Zydus board approved a buyback of up to Rs 1100 crore at Rs 1,150 per share, along with a 100 percent dividend for FY26. Zydus Lifesciences reported a rise in…

Chemists strike on May 20: Reasons behind today’s all-India strike

While major pharmacy chains and government medical outlets will remain operational, the strike highlights significant tensions within the industry that could impact access to medications nationwide. The All India Organisation…

Leave a Reply

Your email address will not be published. Required fields are marked *

You Missed

Zydus Lifesciences Q4FY26 net profit rises 9%

Zydus Lifesciences Q4FY26 net profit rises 9%

Chemists strike on May 20: Reasons behind today’s all-India strike

Chemists strike on May 20: Reasons behind today’s all-India strike

AbbVie loses patent plea for Hep C drug

AbbVie loses patent plea for Hep C drug

GSK’s Calpol a well-known trademark: High Court

GSK’s Calpol a well-known trademark: High Court

3 arrested for allegedly posing as doctors using forged MBBS degrees

3 arrested for allegedly posing as doctors using forged MBBS degrees

Commissioner FDA reviews enforcement measures

Commissioner FDA reviews enforcement measures