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<root>
    <author>ENA</author>
    <category>MSME</category>
    <date>2025-02-13 13:43:32</date>
    <fulldesc>&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;&lt;strong&gt;New Delhi, Feb 13 (KNN)&lt;/strong&gt; The Union Health Ministry has extended the deadline for small and medium-sized pharmaceutical companies to comply with revised Schedule M standards, granting them until December 31, 2025, to meet the new quality and manufacturing requirements. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;This extension applies specifically to pharmaceutical units with annual turnover below Rs 250 crore, affecting approximately 8,500 companies in the MSME category.&lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;The revised Schedule M standards, introduced in December 2023, aim to align Indian pharmaceutical manufacturing practices with global standards, particularly those of the World Health Organisation (WHO). &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;While larger pharmaceutical companies with annual turnover exceeding Rs 250 crore were given a six-month compliance window, MSME units initially received a twelve-month period. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;Industry associations, including the Federation of Healthcare Professionals and Laghu Udyog Bharati, had originally requested an extension until December 2026, citing challenges in financing new machinery and training personnel.&lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;The significance of this compliance is particularly relevant given India's position as a major medicine supplier to low and middle-income countries (LMICs), which require WHO Good Manufacturing Practice (GMP) certification. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;Currently, only about 2,000 units in the MSME category possess this certification, highlighting the substantial upgrade requirements facing the sector.&lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;The extension comes with specific conditions, as outlined in the ministry's formal notification amending the Drugs Rules, 1945. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;Small pharmaceutical companies must submit an online application to the Central Licensing Approval Authority within three months of the notification's publication, including a detailed plan for facility upgradation. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;The ministry has emphasised that these facilities will undergo audits after the three-month period, with potential consequences for companies failing to implement their committed upgrades.&lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;Industry experts note that this extension affects the majority of India's pharmaceutical manufacturing sector, as approximately 8,500 of the country's 10,500 pharmaceutical units operate within the MSME category. &lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;span style=&quot;font-size:14px&quot;&gt;The new timeline establishes January 1, 2026, as the unified date for all pharmaceutical units in India to conform to the revised Schedule M standards, marking a significant milestone in the country's pharmaceutical manufacturing quality standards.&lt;/span&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;em&gt;&lt;strong&gt;&lt;span style=&quot;font-size:14px&quot;&gt;(KNN Bureau)&lt;/span&gt;&lt;/strong&gt;&lt;/em&gt;&lt;br /&gt;&#13;
 &lt;/p&gt;&#13;
</fulldesc>
    <id>41047</id>
    <link>https://knnindia.co.in/news/newsdetails/msme/schedule-m-compliance-deadline-for-pharma-msmes-extended-to-31-dec-2025</link>
    <pubDate>2025-02-13 13:43:32</pubDate>
    <source>knnindia.co.in</source>
    <title>Schedule-M Compliance Deadline For Pharma MSMEs Extended To 31 Dec, 2025</title>
</root>
