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eLiquid GMP Consulting specializes in compliance for upcoming and current regulatory requirements.
Who We Are
Drawing on unmatched experience, specialized knowledge, and a collaborative, action-oriented approach, eLiquidGMP will deliver customized quality and compliance solutions to the eLiquid industry.
We assist our clients in achieving regulatory compliance and excellence using a trifecta approach: Manufacturing audits, regulatory excellence, and analytical transparency. By infusing our consulting and laboratory services with the utmost attention to detail, we will place you and your company on a path to successfully meeting compliance while maintaining a minimal cost structure. Let’s get to work!!!
What We Do
- FDA compliance for Tobacco Products (21CFR Part 1100,1400 and 1450)
- Premarket Tobacco Application Submission (PMTA)
- Tobacco Products Directives (TPD) Submission and compliance (European Union)
- Implementation of Quality Management System (QMS)
- Implementation of ISO program and ISO Audit and Inspection
- Labeling and packaging compliance for FDA and EU
- Quality Audit and Inspection and Suppliers Assessment
- Full Suite Analytical services for Eliquid utilizing GC/MS, HPLC, HS/GC/FID, ICP-MS
- Establish Safety Policies and Program for manufacturers to comply with OHSA/US EPA/EU ECHA
- Employees Training Program for Quality and Safety
Testimonials
Our Happy Clients!
Latest News and Updates
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...
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...
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,...
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)...
Contact Us
We are so very excited to make your acquaintance!
Please feel free to give us a ring in the office, send us an email, or chat with us on social media!!!