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CloneICP

Find regulatory consultants by submission type and agency.

Describe the regulatory expertise your program needs. Get consultants who have navigated the exact submission types your program requires.

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3 free searches — discover 60-150 matching professionals, no signup required

Then $1 per search

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Your gene therapy program needs a consultant with CBER experience filing INDs through the Office of Tissues and Advanced Therapies. The RAPS directory lists 'regulatory affairs' as a practice area. That is not the same thing.

The wrong regulatory consultant does not just waste money -- they can set your development program back by years. A 510(k) specialist has no business advising on your BLA. Someone with deep FDA experience may have zero familiarity with EMA scientific advice procedures. The specificity matters enormously: submission type, agency division, therapeutic area, and regulatory pathway form a combination that standard directories cannot match. That expertise may live in a former CBER reviewer who left three years ago and started an independent consultancy.

Describe the exact combination: submission type, agency division, therapeutic area, and pathway. CloneICP finds 20-50 consultants whose agency experience and career trajectories match what your program actually requires.

Twelve 510(k) submissions does not qualify someone for your BLA.

See what you get

What You Get

What You'll Get

Every search returns clear output in under 60 seconds.

20-50 Regulatory Consultants

Professionals whose agency experience, submission types, and therapeutic area expertise match your program's regulatory needs.

Match Scores

Each consultant ranked by how closely their regulatory background aligns with your specific pathway and agency requirements.

Why They Match

Specific signals: agency division experience, submission types, therapeutic area, former agency roles, career trajectory.

CSV Export

Download your candidate list. Share with your regulatory leadership for evaluation and conflict-of-interest review.

How It Works

01

Describe Your Target

Tell us who you're looking for in plain language.

02

AI Finds Matches

We analyze signals and find matching professionals.

03

Export Results

Up to 50 matches, ready for your enrichment tool.

How This Is Different

RAPS listings tell you someone does regulatory affairs. Not which submissions they have actually filed.

With RAPS directory & industry networks
  • RAPS member listings organize by broad practice area, not by specific submission type or agency division
  • Conference networking surfaces well-known consultants, not specialists in narrow regulatory pathways
  • Retained search firms draw from their existing networks of former agency officials
  • No systematic way to search for consultants by specific agency division and submission experience
With CloneICP
  • Describe the exact regulatory pathway, agency division, and therapeutic area you need
  • Find former agency reviewers and specialized consultants outside the usual conference circuit
  • Discover consultants at independent practices and mid-size CROs with directly relevant experience
  • Results based on publicly available career histories and professional information

Questions

Can this find former FDA or EMA reviewers who have moved into consulting?
Yes. Describe the agency division and review experience you are looking for. Many former agency scientists and reviewers transition to independent consulting or join regulatory affairs firms. Their career trajectories are reflected in publicly available professional information, which means they appear in results when their backgrounds match your description.
How specific can I be about submission types and regulatory pathways?
Very specific. Describe the submission type (IND, NDA, BLA, 510(k), De Novo, PMA, MAA), the regulatory pathway (accelerated approval, breakthrough therapy, fast track, PRIME), the target agency division, and the therapeutic area. The more precisely you describe what your program needs, the more relevant the results.
Is this useful for global regulatory strategy, not just FDA?
Yes. Describe the agencies and regions relevant to your program. Consultants with EMA scientific advice experience, PMDA consultation backgrounds, Health Canada review history, or multi-regional regulatory strategy expertise appear in results when their professional profiles match your description.
How much does it cost?
3 free searches to start, no signup required. After that, credits start at $10 for 10 searches. No subscription needed.

Try It Free

3 searches. No signup. Results in under 60 seconds.

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