Regulatory Compliance
I plan compliance from the beginning through our network of accredited labs so it doesn't delay your launch.
Compliance discovered too late kills more launches than bad design.
Founders treat compliance as a final checkbox — something to handle after the product is designed and produced. But regulations affect material selection, component choices, and even product architecture. Discovering FDA requirements six weeks before ship date forces redesigns, delays, and wasted lab fees.
The pattern repeats: untested samples submitted to labs, market-specific requirements missed, and certifications left to expire because no one tracked renewal deadlines.
- Planning compliance after production starts, forcing redesigns or launch delays
- Submitting untested samples to labs, resulting in failures and wasted fees
- Missing market-specific requirements (e.g., UKCA for post-Brexit Britain)
- Letting certifications expire without tracking renewal deadlines
Market Compliance Mapping
Identification of all applicable regulations, certifications, and testing requirements for your product category and target markets — before you commit to production.
Lab Testing Coordination
Test sample submission and management with accredited third-party laboratories — SGS, Intertek, Bureau Veritas — with timeline management built around your production schedule.
Technical File Preparation
Technical documentation, declarations of conformity, and test reports compiled into market-ready compliance files for CE, FCC, FDA, UKCA, and equivalent frameworks.
Ongoing Compliance Monitoring
Regulatory change monitoring for your product categories — ensuring your certifications remain current as standards evolve.
Compliance Mapping
I identify every regulation and testing requirement for your target markets before design is locked — assessing mandatory vs. recommended certifications.
Lab Testing Coordination
I manage sample submission and coordination with accredited labs (SGS, Intertek, Bureau Veritas), aligned with your production milestones.
Documentation & Monitoring
Complete technical files compiled for CE, FCC, FDA, UKCA. Ongoing regulatory change alerts and renewal reminders keep certifications current.
Compliance is not a final checkbox. It is a design constraint that should shape every decision from day one.
The right time to plan for certification is during product specification, not after the golden sample is approved.
I map requirements early, coordinate directly with accredited labs in our network, and prepare the documentation you need for import and retail.
What Makes Our Approach Different
- Compliance planning begins during specification — not after the golden sample
- Direct coordination with accredited labs, not handoffs to third parties
- All documentation compiled into a single, audit-ready file
Common Questions
During product specification, before design is locked. Regulations affect material selection, component choices, and product architecture — all cheaper to address early.
SGS, Intertek, and Bureau Veritas — accredited labs with global recognition. we manage sample submission and coordinate directly with them, not through third parties.
Typically 4–12 weeks depending on product and certification type. we build this into your production timeline from the start.
Yes. we track regulatory changes, renewal deadlines, and certificate status. You receive alerts before anything expires.