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Halloran Consulting Group

Halloran Consulting Group is a life-sciences consulting firm providing regulatory strategy, dossier writing, GxP quality, and clinical trial management.

At a glance

Delivery model

Consulting / Advisory FirmService ProviderCRO / Research Services Provider

Main areasCapabilities

34 reviewed capabilities
Reviewed Oct 2026
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Halloran Consulting Group is a life science consulting firm that provides regulatory, quality, and clinical support to pharma and medical device companies, from early development to commercialization. Its work includes agency interactions, regulatory content, inspection readiness, trial oversight, and organizational strategy.

Regulatory Strategy and Submissions

  • Develop regulatory strategies and support agency interactions, including advice informed by frequent FDA engagement.
  • Prepare regulatory content such as Module 2 summaries, protocols, and investigator brochures, and support IND, BLA, NDA, and MAA applications. Halloran also provides eCTD document formatting, publishing, assembly, and submission support, reviews CMC filing documents, guides 510(k) applications for medical devices, and serves as an authorized FDA representative.

Quality, Compliance and Inspection Readiness

  • Build or assess GxP quality management systems, identify compliance gaps, prioritize risk-based actions, and develop implementation plans, procedures, and CAPA responses.
  • Prepare for regulatory inspections through virtual or on-site readiness engagements, conduct GxP audits of clinical vendors and suppliers, and provide support for data integrity, 21 CFR Part 11, and computer system validation.

Clinical Development and Strategy

  • Plan and oversee clinical studies through protocol and synopsis development, bottom-up budgets, scenario planning, study start-up, vendor selection, and clinical trial project management for timelines and milestones.
  • Evaluate indications and business opportunities through risk, cost, and commercial assessments; support due diligence led by drug development experts and advise on organizational design and change adoption.

Best Fit

  • Biopharmaceutical and medical device teams seeking consulting support for regulatory submissions, FDA interactions, GxP quality systems, audits, or inspection preparation.
  • Organizations planning or managing clinical studies that need project leadership, study-start-up support, vendor oversight, budgeting, or development strategy.

Reviewed capability coverage

Backed by 22 pages from the vendor's own site. Select a capability to see its quote and source.

Main offeringWhat the vendor leads with
Corporate Strategy & Enterprise7 capabilities
Strategy & Consulting

Corporate, Portfolio & Innovation Strategy

Operating Model, Transformation & Digital Strategy

Product, Launch & Market Expansion Strategy

Business Development, Licensing & Transactions

Life Sciences Enterprise Services

HR, Payroll, Learning & Talent Acquisition

Regulatory, Quality & Safety21 capabilities
Regulatory Affairs & Submissions

Regulatory Strategy & Agency Interactions

Regulatory Writing, CMC, Labeling & Artwork

Clinical & Marketing Applications

Regulatory Operations, Publishing & Information Management

Device/IVD Regulatory Affairs & Regulatory Technology

Quality, GxP & Validation

GxP Compliance, Quality Risk & Product Quality

QMS, CAPA, Change & Document Controls

Audits, Supplier Quality & Inspection Readiness

CSV, Data Integrity & Process Validation

Quality Training & Platform Implementation

Pharmacovigilance & Drug Safety

PV Outsourcing, Governance & Compliance

Clinical Development & Operations5 capabilities
Clinical Trial Operations & eClinical Technology

CRO, Trial Management & Study Start-Up

Clinical Development Strategy & Study Design

Clinical Development & Protocol Strategy

Trial Budgeting & Forecasting

Medical Affairs, Evidence & Access1 capability
Medical Affairs & Scientific Communications

Medical Affairs Strategy, Operations & Integrated Evidence

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