
SDS Authoring for Pharmaceutical & Biotech Applications
Quantum SDS offers expert SDS authoring for finished pharma products, APIs, intermediates, and biotech reagents. Our team handles toxicological profiles, experimental data, and global compliance with precision.
Services Include:
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SDSs for clinical and research-grade substances
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Exposure control guidance and risk assessment notes
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REACH Annex II and ICH compatibility
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Confidential handling of unpublished ingredients
Compliant SDSs for controlled substances, investigational drugs, and complex biotech products.
Regulations That Apply to Pharma & Biotech
OSHA Hazard Communication Standard (29 CFR 1910.1200)
Fully exempts drugs in solid final form for direct administration to a patient; active ingredients, intermediates and research-grade substances are not exempt.
EU REACH Regulation (EC) No 1907/2006
Annex II sets the safety data sheet format and content required across the EU.
Hazardous Products Act, Schedule 1
Excludes drugs regulated under the Food and Drugs Act from the WHMIS supplier requirements.
EU CLP Regulation (EC) No 1272/2008
Governs classification and labelling for APIs and intermediates placed on the EU market.
Regulatory references reviewed August 2026, each linked to its primary source. This page is general information about the documentation Quantum SDS produces, not compliance advice, and requirements change — confirm the current rule that applies to your product before relying on it, or talk to our team.
Solutions for Pharma & Biotech
SDS Authoring
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Other Industries We Serve
Petroleum & Lubricants
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Let’s Get Your SDSs Compliant
Quantum SDS gives you the authoring tools and expertise to create compliant Safety Data Sheets for any market—localized, accurate, and ready in 43+ languages.