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Global Regulatory Strategy
ICON’s Regulatory Consulting Solutions team has expertise in all aspects of drug, biologic, cell and gene therapies across a range of therapeutic indications.
We offer full-service development and regulatory consultancy, providing both strategic and operational support throughout the product development life cycle, covering preclinical/ analytical and clinical trial evaluation, marketing authorisation and post-approval maintenance.
The team works as part of the ICON clinical development organisation, as well as independently on standalone consulting projects for our clients. Our operational model is flexible, to adapt to individual client project requirements.
Key services
Strategic regulatory consulting:
- Provide strategic guidance and operational execution across service lines and throughout the product lifecycle
- In-country expertise and regulatory consulting: US (FDA), EU (EMA), Canada (HC), Korea (MFDS), China (NMPA), Japan (PMDA) and Australia (TGA)
- Risk evaluation and mitigation strategy/ risk management plan consulting
- Due diligence
Health authority interactions:
- Act as global agency liaison ‘agent’ as needed (e.g. US and Canada)
- Support global agency/ advisory meetings
- Scientific advice
Regulatory expertise:
- Program lead for US Investigational New Drug (IND) applications and maintenance, Canada Clinical Trial Applications and marketing authorisation applications
- Expedited pathways (e.g. accelerated, priority, breakthrough, fast track, qualified infectious disease product designation, PRIME, innovative licensing and access pathway)
- Orphan drug/ rare paediatric diseases designations
- Gap analysis
- Paediatric investigation/ study plan
Regulatory writing/ review:
- Module 2 clinical and non-clinical summaries
- Investigator brochures
- Briefing books
- Protocol and study report writing
Post-marketing regulatory affairs support
In this section
In this section
- Asset Development Consulting
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Blended Solutions
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Cardiac Safety Solutions
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Clinical & Scientific Operations
- Biostatistics
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Case studies
- Clinical Operations
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Clinical Supplies Management
- COVID-19
- Clinical data science
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Endpoint Adjudication Services
- Global Logistics
- Interactive Response Technology
- Investigator Payments
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Medical Affairs
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Medical Call Centre Services
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Medical Writing & Publishing
- Pharmacovigilance
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Project and Program Management
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Site Identification and Feasibility
- Commercial Positioning
- Decentralised Clinical Trials
- Early Clinical
- Language Services
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Laboratories
- Medical Imaging
- Outcome Measures
- Real World Intelligence
- Regulatory Affairs
- Symphony Health data
- Site & Patient Solutions
- Strategic Solutions
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Technologies