Deprecated (16384): The ArrayAccess methods will be removed in 4.0.0.Use getParam(), getData() and getQuery() instead. - /home/brlfuser/public_html/src/Controller/ArtileDetailController.php, line: 73
 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php. [CORE/src/Core/functions.php, line 311]
Code Context


        trigger_error($message, E_USER_DEPRECATED);

    }
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 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php.'
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deprecationWarning - CORE/src/Core/functions.php, line 311
Cake\Http\ServerRequest::offsetGet() - CORE/src/Http/ServerRequest.php, line 2421
App\Controller\ArtileDetailController::printArticle() - APP/Controller/ArtileDetailController.php, line 73
Cake\Controller\Controller::invokeAction() - CORE/src/Controller/Controller.php, line 610
Cake\Http\ActionDispatcher::_invoke() - CORE/src/Http/ActionDispatcher.php, line 120
Cake\Http\ActionDispatcher::dispatch() - CORE/src/Http/ActionDispatcher.php, line 94
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Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\RoutingMiddleware::__invoke() - CORE/src/Routing/Middleware/RoutingMiddleware.php, line 162
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\AssetMiddleware::__invoke() - CORE/src/Routing/Middleware/AssetMiddleware.php, line 88
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Error\Middleware\ErrorHandlerMiddleware::__invoke() - CORE/src/Error/Middleware/ErrorHandlerMiddleware.php, line 96
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Http\Runner::run() - CORE/src/Http/Runner.php, line 51
Cake\Http\Server::run() - CORE/src/Http/Server.php, line 98

Deprecated (16384): The ArrayAccess methods will be removed in 4.0.0.Use getParam(), getData() and getQuery() instead. - /home/brlfuser/public_html/src/Controller/ArtileDetailController.php, line: 74
 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php. [CORE/src/Core/functions.php, line 311]
Code Context


        trigger_error($message, E_USER_DEPRECATED);

    }
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 You can disable deprecation warnings by setting `Error.errorLevel` to `E_ALL & ~E_USER_DEPRECATED` in your config/app.php.'
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deprecationWarning - CORE/src/Core/functions.php, line 311
Cake\Http\ServerRequest::offsetGet() - CORE/src/Http/ServerRequest.php, line 2421
App\Controller\ArtileDetailController::printArticle() - APP/Controller/ArtileDetailController.php, line 74
Cake\Controller\Controller::invokeAction() - CORE/src/Controller/Controller.php, line 610
Cake\Http\ActionDispatcher::_invoke() - CORE/src/Http/ActionDispatcher.php, line 120
Cake\Http\ActionDispatcher::dispatch() - CORE/src/Http/ActionDispatcher.php, line 94
Cake\Http\BaseApplication::__invoke() - CORE/src/Http/BaseApplication.php, line 235
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\RoutingMiddleware::__invoke() - CORE/src/Routing/Middleware/RoutingMiddleware.php, line 162
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Routing\Middleware\AssetMiddleware::__invoke() - CORE/src/Routing/Middleware/AssetMiddleware.php, line 88
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Error\Middleware\ErrorHandlerMiddleware::__invoke() - CORE/src/Error/Middleware/ErrorHandlerMiddleware.php, line 96
Cake\Http\Runner::__invoke() - CORE/src/Http/Runner.php, line 65
Cake\Http\Runner::run() - CORE/src/Http/Runner.php, line 51
Cake\Http\Server::run() - CORE/src/Http/Server.php, line 98

Warning (512): Unable to emit headers. Headers sent in file=/home/brlfuser/public_html/vendor/cakephp/cakephp/src/Error/Debugger.php line=853 [CORE/src/Http/ResponseEmitter.php, line 48]
Code Context
            if (Configure::read('debug')) {

                trigger_error($message, E_USER_WARNING);

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</span></span></code>
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&amp;rsquo;s drug regulators had broken laws, ignoring the interests of patients.&lt;br /&gt;
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The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.&lt;br /&gt;
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                <strong>Doc panel for drug approval</strong></h1>
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                -The Telegraph<br /><div align="justify"><br />The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.<br /><br />The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.<br /><br />The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.<br /><br />The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.<br /><br />The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.<br /><br />Medicines used to treat myriad illnesses &mdash; from infections to cancer, from liver disease to sexual dysfunction &mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.<br /><br />The ministry has asked the three-member panel to recommend steps to bring about &ldquo;systemic improvements&rdquo; in drug approval procedures and to &ldquo;institutionalise improvements&rdquo; in the procedural aspects of the functioning of the CDSCO.<br /><br />A senior public health expert said the panel should ideally have included &ldquo;representatives of civil society&rdquo; who are familiar with these issues.</div>               </font>
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</span></span></code>
<span class="code-highlight"><code><span style="color: #000000">&nbsp;&nbsp;&nbsp;&nbsp;&lt;link&nbsp;rel="canonical"&nbsp;href="<span style="color: #0000BB">&lt;?php&nbsp;</span><span style="color: #007700">echo&nbsp;</span><span style="color: #0000BB">Configure</span><span style="color: #007700">::</span><span style="color: #0000BB">read</span><span style="color: #007700">(</span><span style="color: #DD0000">'SITE_URL'</span><span style="color: #007700">);&nbsp;</span><span style="color: #0000BB">?&gt;&lt;?php&nbsp;</span><span style="color: #007700">echo&nbsp;</span><span style="color: #0000BB">$urlPrefix</span><span style="color: #007700">;</span><span style="color: #0000BB">?&gt;&lt;?php&nbsp;</span><span style="color: #007700">echo&nbsp;</span><span style="color: #0000BB">$article_current</span><span style="color: #007700">-&gt;</span><span style="color: #0000BB">category</span><span style="color: #007700">-&gt;</span><span style="color: #0000BB">slug</span><span style="color: #007700">;&nbsp;</span><span style="color: #0000BB">?&gt;</span>/<span style="color: #0000BB">&lt;?php&nbsp;</span><span style="color: #007700">echo&nbsp;</span><span style="color: #0000BB">$article_current</span><span style="color: #007700">-&gt;</span><span style="color: #0000BB">seo_url</span><span style="color: #007700">;&nbsp;</span><span style="color: #0000BB">?&gt;</span>.html"/&gt;
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&amp;rsquo;s drug regulators had broken laws, ignoring the interests of patients.&lt;br /&gt;
&lt;br /&gt;
The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.&lt;br /&gt;
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The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.&lt;br /&gt;
&lt;br /&gt;
The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.&lt;br /&gt;
&lt;br /&gt;
The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.&lt;br /&gt;
&lt;br /&gt;
Medicines used to treat myriad illnesses &amp;mdash; from infections to cancer, from liver disease to sexual dysfunction &amp;mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.&lt;br /&gt;
&lt;br /&gt;
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&lt;br /&gt;
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&lt;br /&gt;
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                <strong>Doc panel for drug approval</strong></h1>
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                -The Telegraph<br /><div align="justify"><br />The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.<br /><br />The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.<br /><br />The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.<br /><br />The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.<br /><br />The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.<br /><br />Medicines used to treat myriad illnesses &mdash; from infections to cancer, from liver disease to sexual dysfunction &mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.<br /><br />The ministry has asked the three-member panel to recommend steps to bring about &ldquo;systemic improvements&rdquo; in drug approval procedures and to &ldquo;institutionalise improvements&rdquo; in the procedural aspects of the functioning of the CDSCO.<br /><br />A senior public health expert said the panel should ideally have included &ldquo;representatives of civil society&rdquo; who are familiar with these issues.</div>               </font>
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&amp;rsquo;s drug regulators had broken laws, ignoring the interests of patients.&lt;br /&gt;
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The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.&lt;br /&gt;
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The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.&lt;br /&gt;
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&lt;br /&gt;
Medicines used to treat myriad illnesses &amp;mdash; from infections to cancer, from liver disease to sexual dysfunction &amp;mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.&lt;br /&gt;
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&lt;br /&gt;
The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.&lt;br /&gt;
&lt;br /&gt;
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&lt;br /&gt;
The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.&lt;br /&gt;
&lt;br /&gt;
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&lt;br /&gt;
Medicines used to treat myriad illnesses &amp;mdash; from infections to cancer, from liver disease to sexual dysfunction &amp;mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.&lt;br /&gt;
&lt;br /&gt;
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.

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                <strong>Doc panel for drug approval</strong></h1>
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                -The Telegraph<br /><div align="justify"><br />The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.<br /><br />The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.<br /><br />The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.<br /><br />The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.<br /><br />The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.<br /><br />Medicines used to treat myriad illnesses &mdash; from infections to cancer, from liver disease to sexual dysfunction &mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.<br /><br />The ministry has asked the three-member panel to recommend steps to bring about &ldquo;systemic improvements&rdquo; in drug approval procedures and to &ldquo;institutionalise improvements&rdquo; in the procedural aspects of the functioning of the CDSCO.<br /><br />A senior public health expert said the panel should ideally have included &ldquo;representatives of civil society&rdquo; who are familiar with these issues.</div>               </font>
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.<br />
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The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.<br />
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The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.<br />
<br />
The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.<br />
<br />
The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.<br />
<br />
Medicines used to treat myriad illnesses &mdash; from infections to cancer, from liver disease to sexual dysfunction &mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.<br />
<br />
The ministry has asked the three-member panel to recommend steps to bring about &ldquo;systemic improvements&rdquo; in drug approval procedures and to &ldquo;institutionalise improvements&rdquo; in the procedural aspects of the functioning of the CDSCO.<br />
<br />
A senior public health expert said the panel should ideally have included &ldquo;representatives of civil society&rdquo; who are familiar with these issues.
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.<br />
<br />
The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market.<br />
<br />
The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures.<br />
<br />
The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.<br />
<br />
The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived.<br />
<br />
Medicines used to treat myriad illnesses &mdash; from infections to cancer, from liver disease to sexual dysfunction &mdash; had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts.<br />
<br />
The ministry has asked the three-member panel to recommend steps to bring about &ldquo;systemic improvements&rdquo; in drug approval procedures and to &ldquo;institutionalise improvements&rdquo; in the procedural aspects of the functioning of the CDSCO.<br />
<br />
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The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India&rsquo;s drug regulators had broken laws, ignoring the interests of patients.

The panel announced by the...'
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Doc panel for drug approval

-The Telegraph The Centre today asked a panel of doctors to outline measures to improve drug approval procedures, three days after a parliamentary standing committee said India’s drug regulators had broken laws, ignoring the interests of patients. The panel announced by the Union health ministry has been asked to suggest steps to improve the procedural aspects of the Central Drugs Standards Control Organisation (CDSCO), the agency entrusted with approving medicines for sale in the Indian market. The report tabled in Parliament on Tuesday had observed that the CDSCO has approved a large number of drugs either without any clinical trials in India or through irregular approval procedures. The panel, which will also examine the guidelines adopted to approve drugs without clinical trials, has been given two months to submit its report. Its three members are P.N. Tandon, president of the National Brain Research Centre, Manesar, V.M. Katoch, director general of the Indian Council of Medical Research, New Delhi, and S.S. Agarwal, former director of the Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow. The standing committee had also found that government doctors and private practitioners living in different cities had written near identical letters endorsing certain drugs or recommending that clinical trials be waived. Medicines used to treat myriad illnesses — from infections to cancer, from liver disease to sexual dysfunction — had been approved by CDSCO officials through irregular procedures, at times even without any consultations with medical experts. The ministry has asked the three-member panel to recommend steps to bring about “systemic improvements” in drug approval procedures and to “institutionalise improvements” in the procedural aspects of the functioning of the CDSCO. A senior public health expert said the panel should ideally have included “representatives of civil society” who are familiar with these issues.