Leading the way in CTO, CRO and CDMO Solutions
Via a CTO, CRO or CDMO, projects are supported by dedicated scientific experts who are highly skilled and experienced in driving scientific research, development and delivery forward.
The role of CTOs, CROs and CDMOs can be scaled up, or scaled back, in accordance with the requirements of an organisation, the demand of their projects and the level of support their teams require.
CTOs, CROs and CDMOs work to set scientific regulations and standards, ensuring all projects – and their discoveries and outputs – adhere to all necessary requirements.
What are Contract Testing Organisations (CTOs), Contract Research Organisations (CROs) and Contract Development and Manufacturing Organisations (CDMOs)?
Contract Testing Organisations (CTOs), Contract Research Organisations (CROs) and Contract Development and Manufacturing Organisations (CDMOs) are essential in scientific and pharmaceutical industries.
CROs specialise in research and development activities, providing services including preclinical research, clinical trials, and regulatory consulting, empowering companies to focus on their core goals while accelerating innovation.
The role of CDMOs is in the development and manufacturing of pharmaceutical products, including formulation, scale-up production, packaging, and distribution, ensuring flexibility, scalability, and compliance with regulatory standards.
CTOs offer specialised analytical and quality assurance services, conducting rigorous testing to ensure the safety, efficacy, and compliance of pharmaceutical products with regulatory standards. They assist in areas such as stability testing, method validation, raw material analysis, and contamination control, providing pharmaceutical companies with reliable data and insights critical for product approval and market release.
Each organisation provides expert scientific support, enabling laboratories and scientific teams to scale operations according to project needs while maintaining high levels of quality and adherence to regulations. The skilled professionals and advanced infrastructure of CTOs, CROs and CDMOs ensure precision in research, development, and manufacturing processes, helping companies remain competitive and deliver high-quality results.
Click here to find out about the several CTO, CRO and CDMO models to choose from
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Specialised CTO: Focuses on high-demand analytical services and regulatory expertise for niche industry requirements.
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On-Demand CTO: Offers flexible, project-based testing solutions tailored to the scope and timeline of organisational needs.
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Integrated CTO: Ensures seamless collaboration with existing teams to deliver customised testing programs aligned with company objectives and processes.
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End-to-End CTO: Provides comprehensive testing services, from initial analysis to method validation and ongoing quality assurance support.
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Full-Service CRO: Provides comprehensive research and development services from preclinical studies to clinical trials and regulatory consulting.
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Hybrid CRO: Combines elements of full-service and functional models, tailoring services to meet the unique needs of clients and projects.
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End-to-End CDMO: Offers complete product development and manufacturing solutions, including formulation, scale-up production, and packaging.
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Specialised CDMO: Concentrates on niche areas such as biologics or advanced drug delivery systems, leveraging expertise in specific domains.
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Integrated CDMO: Aligns development and manufacturing processes to ensure seamless transition and operational efficiency across product life cycles.
Why choose SRG
We understand the unique needs of Life Sciences employers. SRG delivers solutions tailored to the fast-paced, high-demand world of science. Our embedded teams work as an extension of your business, combining strategic insight with day-to-day recruitment and workforce delivery — helping you attract top talent, increase efficiency, and improve the candidate experience.
We provide expert scientific support for your research, development and manufacturing projects, working to your requirements and objectives, in line with your culture and ways of working.
Benefits of partnering with us
Our clients in Life Sciences sectors gain measurable advantages from SRG’s expert-led CTO, CRO and CDMO services, which are built to deliver consistent results in a competitive market:
Access to Hard-to-Find Talent
We maintain extensive networks of skilled professionals across drug development, manufacturing, regulatory, quality, and commercial functions. Whether you need experts in biologics, cell and gene therapy, or GMP manufacturing, we know where to find them, often before they hit the open market.
Industry Expertise
We understand the science, the regulatory frameworks, and the urgency behind every hire. Our team speaks the same language as your hiring managers and can accurately assess candidates for technical fit and regulatory readiness.
Faster, Smarter Hiring
Time is critical, especially when scaling up for new projects or expanding manufacturing capacity. Our specialist approach means faster shortlisting, targeted outreach, and less time wasted on unqualified applicants.
Quality Hires
Beyond technical skills, we assess candidates for adaptability, client-facing communication, and cross-functional collaboration, traits that are essential in CDMO/CRMO environments. Our placements are not just made quickly; we make them to last.
Valuable Market Insights
We provide more than talent. We deliver data. From salary benchmarks and hiring trends to talent availability by region, we equip you with insights that help you stay competitive and make informed decisions.
Flexible Support for Growth and Project Spikes
Need to scale quickly for a new client project or facility launch? We can support contract, interim, and permanent hires, scaling up or down as needed without overwhelming your internal teams
Need talent or looking to find your next opportunity?
Let’s talk. Whether you're hiring or job searching, fill out our contact form and one of our specialist consultants will be in touch.
