Regulatory Information

Comprehensive Regulatory Information for all DRAVYOM chemical products. Access detailed safety information, handling procedures, and technical specifications to ensure safe and effective use of our chemicals.

Regulatory Information

Compliance documentation and regulatory guidelines

ISO Compliance Certificates

Official ISO 9001:2015 Quality Management System certificates, ISO 14001:2015 Environmental Management certification, and ISO 45001:2018 Occupational Health & Safety Management System documentation with audit reports and continuous improvement records.

Updated: May 2025 PDF Format Valid Until 2026
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REACH & GHS Compliance

Complete REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance documentation, GHS classification reports, EU regulatory submissions, and pre-registration confirmations for European market access.

Updated: April 2025 PDF Format EU Compliant
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GMP & Quality Assurance

Good Manufacturing Practice (GMP) compliance documentation, pharmaceutical grade quality systems, batch release procedures, deviation management protocols, and validated manufacturing process documentation for pharmaceutical applications.

Updated: May 2025 PDF Format Pharma Grade
Download Framework

Transportation & Shipping Compliance

UN/ADR dangerous goods classification, IATA air transport regulations, IMDG maritime shipping requirements, packaging specifications, hazard labeling guidelines, and international shipping documentation for safe chemical transport.

Updated: March 2025 PDF Format Global Shipping
Download Guide

Environmental Impact Assessment

Environmental compliance reports, waste management protocols, emission control documentation, biodegradability studies, ecological risk assessments, and sustainability initiatives aligned with global environmental standards.

Updated: April 2025 PDF Format Eco-Friendly
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Regulatory Audit Reports

Third-party regulatory audit findings, corrective action records, compliance verification reports, inspection readiness checklists, and continuous improvement documentation demonstrating ongoing regulatory excellence.

Updated: May 2025 PDF Format Audited
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