COMPLIANT RAW MATERIALS

Do you quarantine and test your raw materials before allowing them to be used for manufacturing finished products? Under the new regulation, it will be required to qualify raw materials prior to using them. We have partnered with analytical experts that are focused solely on e-liquids, ensuring you have analyses that are tailored for your …

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AUDIT YOUR FACILITY OR COPACKER

EliquidGMP will evaluate your current manufacturing facility and/or co-packer facilities, identify gaps in compliance, then help you develop and execute a comprehensive list of action items, guaranteeing all your facilities meet or exceed regulatory requirements. We are here to guide you, step-by-step, through the entire process. Let’s get started!

PRODUCT DEVELOPMENT

eLiquid GMP is positioned with its immediate partners and in-house recourses to offer a full-suite product development service. Whether your product requires a full revision to eliminate unwanted contaminants, improve vaporizer performance, or develop a closed system containing your product, our expertise positions us to do so in a cost-efficient and time-sensitive manner! During the …

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ISO and cGMP:

The FDA Final Rule 21CFR Part 1100, 1400, and 1430 mandates all e-liquid manufacturers to comply with good manufacturing practices. Eliquid Compliance will establish a Quality Management System (QMS) to conform to contemporary regulatory requirements including ISO 9000 certification. In addition, we are experienced with developing and implementing streamlined, cost-efficient quality plans for new and …

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