<h3>All Service</h3>                    <ul id="menu-services-menu"><li id="menu-item-119"><a href="http://localhost/wordpress/index.php/artificial/">Artificial</a></li>
<li id="menu-item-120"><a href="http://localhost/wordpress/index.php/specialized/">Specialized</a></li>
<li id="menu-item-121"><a href="http://localhost/wordpress/index.php/chemical/">Chemical</a></li>
<li id="menu-item-122"><a href="http://localhost/wordpress/index.php/pathology/">Pathology</a></li>
<li id="menu-item-123"><a href="http://localhost/wordpress/index.php/free-home/">Free Home</a></li>
<li id="menu-item-124"><a href="http://localhost/wordpress/index.php/safe-diagnoses/">Safe diagnoses</a></li>
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            <h3>Get a free quick solution of website</h3>                            
                    <a href="http://localhost/wordpress/contact/" >
                        Contact                    </a>
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		<h4>Compliance Services</h4>
		<p data-wow-delay='350ms'>At ValSquare, we specialize in Computer System Validation (CSV) and regulatory compliance solutions that ensure your computerized systems operate reliably, securely, and in full alignment with global regulatory requirements.
Computer systems play a critical role in product development, manufacturing, testing, and data handling. Our compliance services provide documented evidence that your systems are fit for intended use, maintain data integrity, and consistently perform according to approved specifications.</p>
		<h3 data-wow-delay='300ms'>Ensuring Compliance. Protecting Quality. Reducing Risk.</h3><!-- /.service-details__title -->
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		<p data-wow-delay='350ms'>We follow a structured, risk-based validation approach aligned with FDA, EU, and ISO standards, helping organizations maintain audit readiness while improving operational efficiency and confidence in automated systems.</p><!-- /.service-details__text -->
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					<h4>ValSquare provide compliance solutions based on:</h4>					<p></p>
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																		GAMP5 Risk Based Assessment for Compliant Computerized System								</li>
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																		FDA 21 CFR Part 11 solutions 								</li>
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																		ISO ASTM E2500 solutions								</li>
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																		EU GMP Annex 11 solutions								</li>
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			<h3>Why choose?</h3>			
								<h3>
									<a href="http://localhost/wordpress/services/" >Compliance Standards</a>
								</h3>
								<p>We ensure your systems comply with FDA 21 CFR Part 11, EU GMP Annex 11, and ISO regulatory requirements.</p>
								<h4>
									<a href="http://localhost/wordpress/services/" >Safe &amp; Reliable Systems</a>
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								<p>Our validation ensures data accuracy, system reliability, and controlled access—protecting product quality and patient safety.</p>
                        <h4>What We Validate? </h4>
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                            <p><ul>
  <li>Automated Manufacturing Equipment</li>
  <li>Automated Laboratory Equipment</li>
  <li>Process Control Systems</li>
  <li>Process Analytical Systems</li>
  <li>Manufacturing Execution Systems (MES)</li>
  <li>Laboratory Information Management Systems (LIMS)</li>
  <li>Manufacturing Resource Planning (MRP / ERP) Systems</li>
  <li>Clinical Trial &amp; Data Management Systems</li>
</ul>
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                        <h4>Why Computer System Validation Is Mandatory? </h4>
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                            <p><p>
  Regulatory agencies require validation to ensure product safety and data integrity through automated systems.
</p>
Key Regulations Supported:
<ul>
  <li>FDA – 21 CFR Part 11</li>
  <li>EU GMP – Annex 11</li>
  <li>ISO Certification Requirements</li>
</ul>
Validation confirms that your systems:
<ul>
  <li>Meet intended use</li>
  <li>Perform consistently and accurately</li>
  <li>Support safe, quality-driven decision-making</li>
</ul>
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