TGC takes end-to-end ownership of your product compliance programme. Testing, registration, labelling, certification, and market authorisation - managed by a single dedicated specialist, across every market you need to enter.
Full product compliance is not for every engagement. It is for brands that need more than a one-time review - they need an owner.
You have a product ready to take to market but no internal compliance expertise. TGC becomes your compliance function - scoping the requirements, managing every workstream, and delivering a market-ready product.
Launching in the EU, UK, US, and APAC at the same time means managing different regulatory frameworks, different timelines, and different submission requirements in parallel. TGC manages the full programme with one point of contact.
Testing is delayed, registrations are incomplete, and no one has a clear picture of where things stand. TGC takes over the programme, maps the current state, identifies blockers, and drives each workstream to completion.
You have a testing lab, a regulatory consultant, a labelling agency, and a freight forwarder - all working independently. TGC coordinates across all of them with a single accountable owner, so nothing falls between the gaps.
Some products sit across multiple regulatory categories - a supplement that is also a medical device, a chemical that is also a cosmetic ingredient. TGC manages the multi-framework complexity so your team does not have to.
Regulations change. MoCRA in the US, GPSR in the EU, TGA updates in Australia. TGC monitors regulatory changes across your active markets, flags what affects your products, and manages the update process before it becomes a problem.
TGC covers the full compliance lifecycle. Not isolated tasks - the complete programme, coordinated by one specialist who owns the outcome.
We identify the required tests for your product category and target markets, appoint accredited laboratories, manage the testing process, and deliver the reports and certificates needed for market access.
We manage every registration and notification requirement your product needs to enter each target market - from EU CPNP notifications to US FDA registration to TGA ARTG listings.
We review your product labels against the mandatory requirements of every target market, manage the correction process, and build the technical documentation required for market access and audit.
We handle tariff classification and export control screening for your products across all relevant markets, and monitor regulatory changes that affect your compliance position as they happen.
Not a report. Not a list of recommendations. A managed programme with a dedicated owner who is accountable for your product reaching market compliantly.
A clear scope before any work begins.
Before any work begins, TGC scopes your full compliance programme - what is required, what you already have, what needs to be done, and in what order. You receive a scoped proposal for the programme with a milestone-based timeline. No open-ended billing.
One person accountable for every workstream.
Your dedicated specialist owns your programme from kickoff to market entry. They manage every workstream - testing, registration, labelling, certification - and are your single point of contact across all of them. If something is delayed, they know why. If something needs resolving, they resolve it.
Every document your product needs to clear customs and enter market.
At the end of your programme, you hold every document your product needs: test reports, certificates, registration confirmations, technical files, label sign-offs, SDS, declarations of conformity, and HS classification memos. All organised, all referenced, all yours.
Your compliance position maintained as regulations evolve.
Compliance is not a one-time project. Regulations change, certifications expire, and new markets open up. TGC monitors regulatory changes across your active markets, flags anything that affects your products, and manages the update process before it becomes a problem that stops your shipments.
Most compliance failures do not happen because of a single missed requirement. They happen in the gaps between suppliers who each own one piece and no one owns the whole.
When testing, registration, labelling, and HS classification are managed by different suppliers, no single person has a complete view of where your product stands. Critical dependencies get missed. Parallel workstreams fall out of sync.
When something goes wrong - a delayed registration, a failed test, a customs hold - everyone points to someone else. With a single owner, there is no ambiguity about who is responsible and who resolves it.
Managing multiple compliance suppliers means your operations or regulatory team spends significant time coordinating rather than executing. TGC takes that burden off your team so they can focus on the business.
From scoping call to market-ready product - a structured, milestone-based programme with a single dedicated owner at every stage.
We map your product, target markets, current compliance position, and key timelines. We identify every gap and outline the full programme scope.
You receive a proposal covering every workstream, a milestone-based timeline, and the name of your dedicated specialist. No obligation to proceed.
Your specialist manages every workstream in parallel - testing, registration, labelling, documentation, classification. Regular updates keep you informed at every milestone.
You receive every compliance document, certificate, and registration confirmation. Ongoing monitoring ensures your compliance position stays current as regulations evolve.
"TGC took what felt like an impossible situation and turned it around in record time. They handled the documentation, liaised with the authorities, and had our shipment cleared within two weeks. Their team knows compliance inside out."
"We have expanded into four new markets in 2025, and it would not have been possible without TGC's guidance. From CE Marking to local labelling requirements, they kept us compliant and on schedule."
"We were overwhelmed by the new MoCRA requirements in the US, but TGC broke it down into clear steps and managed the entire process, from ingredient reviews to PIF compilation and more."
Many full product compliance programmes begin with a targeted service. These are the most common starting points.
TGC scopes your full compliance programme and provides a clear proposal - no obligation, no open-ended billing.
Custom scoping - Clear proposal - No obligation
