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Chemistry, Manufacturing and Controls (CMC) and Quality
The ICON CMC and Quality Team provides robust CMC strategies, executed by industry-leading experts.
Our team is adept at designing and delivering CMC programs to take candidates from discovery to early clinical trials, through scale up and optimisation, to process validation and registration. All with hands-on resources to manage implementation.
We apply scientific excellence and regulatory expertise every step of the way. We work with clients on formulations, manufacturing processes and controls, specifications for new chemical and biological entities and new formulations of approved products.
The team’s approach is flexible and collaborative, whether providing a single piece of strategic technical consultancy, or joining your team for the design and implementation of your CMC strategy.
Key services
Operational execution of core services and/ or across service lines:
- Health Canada Drug Establishment License and Importer of Record services
- Genetically Modified Organism applications
- Quality services
- Audit services
Writing and review of CMC packages for all pre- and post-approval submissions (small and large molecules including cell and gene therapies):
- Change controls and impact assessments
- CMC component review, gap analysis and due diligence for Clinical Trail Applications and Marketing Authorisation Applications
- CMC authored documents for Investigational New Drug Applications, Biologics License Application, New Drug Applications and Marketing Authorisation Applications
Development strategy for small molecules:
- Technology transfer
- Active pharmaceutical ingredient development
- Drug product development
Development strategy for biologics:
- Process development (quality target product profile, certificate of analysis and certificate of pharmaceutical product risk assessment) and manufacturing
- Analytical method development
- Process validation
- Life cycle management
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
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Early Clinical
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Bioanalytical Laboratories
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Biometrics
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Clinical Pharmacology
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Clinical Research Facilities
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Adaptive Pharmaceutical Services
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Early Phase Oncology
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Early Phase Patient Studies
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Early Phase Obesity Trials
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PK/PD Modeling and Simulation
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Quality and Compliance
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Quantitative Pharmacology and Pharmacometrics
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Volunteer Recruitment
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Bioanalytical Laboratories
- 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
Related Information
Blog
Accelerating ATMP and CGT: The importance of Regulatory CMC expertise in efficient biologics development
Media Article
Regulatory CMC: Enhancing Biologics Development. Preventing delays and accelerating the progression of these critical therapies
Factsheet
Regulatory CMC
Case Study
Seamless transition and lifecycle management for 50+ marketed products
Media Article
Application of project management strategy to postapproval CMC submissions
Blog