Expert Input – When and Where You Need It Most

Not every regulatory challenge needs a long project. Sometimes, you just need a quick check-in, a second opinion, or help with a single submission step.
Our Micro Consulting format gives you fast, focused access to expert guidance on UKCA, TGA, and Medsafe requirements – without complex contracts or long timelines.

Your Challenges

  • One specific issue is blocking progress
    You’re almost ready to submit – but one requirement or term is unclear.
  • Lack of time for deep research
    You need a fast answer to keep moving, not days of reading regulatory texts.
  • Small team, big responsibilities
    You’re handling multiple roles – and just need expert backup for a key topic.
  • Need to validate your approach
    You want to make sure your regulatory assumptions align with local expectations.

How We Help

  • On-demand sessions with senior consultants
    We provide 30–90-minute expert sessions focused on your exact question or deliverable.
  • Written input or document reviews
    Whether it’s a classification rationale or a GSPR checklist – we review and return actionable feedback fast.
  • No long-term commitment
    Pay per session, per document, or by the hour – scale up or down as needed.
  • APAC & UK regulatory experience
    Get clear input tailored to MHRA (UK), TGA (Australia), or Medsafe (New Zealand) rules.

What Our Micro Consulting Covers

Regional Requirements

Classification Clarification

Clear up confusion on SaMD or device class across UK, AU, and NZ.

Clinical Evaluation & Risk Management

GSPR or Checklist Review

Get feedback on your MDR/UKCA/TGA checklist or safety documentation.

Clinical Evaluation & Risk Management

Regulatory Gap Snapshot

Quick high-level analysis to identify missing or unclear content in your docs.

Cybersecurity Documentation

Validation & Cybersecurity Feedback

Get second opinions on test plans, CBOMs, threat models or validation logic.

Timely Response in Local Time Zones

Submission Strategy Advice

Not sure how to package or present your docs for TGA, Medsafe or MHRA? We help.

In-Country Representation

One-on-One Expert Calls

Book a short call to walk through a blocker or specific question with a senior consultant.

Targeted Help, Without the Overhead

No big project. No long contracts. Just focused regulatory support to help you move forward quickly and confidently — across the UK, Australia, and New Zealand.

Looking for more? Discover how we support your team beyond consulting.

Regulatory Training for Your Team

Regulatory Training for Your Team

Build internal know-how with workshops, online courses, and our Regulatory Accelerator.

Helpful Ressources

Helpful Ressources

Access blog articles, checklists, and updates for UKCA, TGA, and Medsafe.

The People Behind Elevate MedTech

The People Behind Elevate MedTech

Learn who we are and why MedTech teams trust us across UK and APAC.