<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>
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            <h3>Get a free quick solution of website</h3>                            
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                        Contact                    </a>
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		<h4>Compliance Services</h4>
		<p data-wow-delay='350ms'>At ValSquare, we deliver comprehensive Computer System Validation (CSV) and regulatory compliance solutions to ensure your computerized systems operate reliably, securely, and in full compliance with global regulatory requirements. Our compliance approach is risk-based, audit-ready, and aligned with industry best practices.</p>
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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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                        <h4>GAMP 5 Risk-Based Assessment for Compliant Computerized Systems </h4>
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                            <p>We apply a structured, risk-based validation methodology in line with GAMP 5 guidelines to ensure systems are fit for intended use, properly controlled, and compliant with regulatory expectations.</p>
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                        <h4>FDA 21 CFR Part 11 Solutions </h4>
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                            <p>Our solutions ensure compliance with FDA 21 CFR Part 11 requirements, focusing on electronic records, electronic signatures, system security, audit trails, and data integrity.</p>
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                        <h4>ISO ASTM E2500 Solutions </h4>
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                            <p>ValSquare supports validation activities based on ISO ASTM E2500, emphasizing a science- and risk-based approach to verifying automated manufacturing systems and critical process controls.</p>
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                        <h4>EU GMP Annex 11 Solutions </h4>
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                            <p>We help organizations meet EU GMP Annex 11 requirements by validating computerized systems used in regulated environments, ensuring proper documentation, system controls, and ongoing compliance.</p>
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