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CDMO Services

Your Partner for Comprehensive CDMO Capabilities

As a trusted CDMO/CMO partner, we streamline the entire process from concept to commercialization, ensuring regulatory compliance and operational excellence.

Our comprehensive CDMO pharmaceutical capabilities cover every aspect of pharmaceutical development, providing efficient solutions for your success. Partner with SCL Lifesciences to drive your pharmaceutical and mRNA innovations forward with scalable and efficient services.

API Drug Substance Development Icon

API Drug Substance Development & Manufacturing

API Drug Substance Development

Delivering high-quality APIs and specialty chemicals. We offer a broad portfolio, including high-potency molecules and niche generics.

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Analytical Services

Analytical Services

Analytical Services

We provides advanced analytical development services with state-of-the-art labs and 21 CFR Part 11-compliant instruments, ensuring accurate, reliable.

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Here's why we stand out as your ideal CDMO partner

Discover why we are your ideal partner, delivering unmatched expertise, reliability, and innovative solutions.

Driving Innovation
Driving Innovation in Pharmaceutical and mRNA Development
Global Regulatory
Global Regulatory-Approved CDMO Facilities
Research and Development Team
Innovative CDMO Services Backed by Advanced R&D
Regulatory Compliance
Proven Regulatory Compliance Across Major Markets

Questions you may have?

Find answers to the most commonly asked questions about our services.

SCL Lifesciences follows a structured CDMO process, ensuring high-quality API development within a typical timeline of 12-14 months (for lab validated products: 3-6 months and for scale-up and validation: 6 months), depending on project complexity. Our concurrent development and scale-up approach, led by cross-functional teams (CFT) and a dedicated PMO, ensures seamless execution. With state-of-the-art R&D facilities, advanced instrumentation, and a skilled scientific team, we provide robust support for development, troubleshooting, and regulatory compliance.

Yes, SCL Lifesciences offers both scalability and flexibility, supporting pilot-scale batches and large-scale commercial production. Our advanced infrastructure enables a smooth transition from kilogram-level development to large-scale manufacturing, backed by expertise in diverse chemistries, high-potency manufacturing, and analytical method development. With a strong focus on backward integration and process optimization, we ensure efficiency, reliability, and high-quality standards across all stages of production.
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Related Resources

Explore our latest news, case studies, and blog posts for valuable insights and updates.

How Integrated CDMO Solutions Simplify the Drug Development Lifecycle
CDMO

How Integrated CDMO Solutions Simplify the Drug Development Lifecycle

The drug development lifecycle is the complete journey of a pharmaceutical product-from its initial discovery through availability on the market and beyond.

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How CDMOs are leading innovation for pharmaceutical partners
CDMO

How CDMOs are leading innovation for pharmaceutical partners

The pharmaceutical industry is undergoing rapid transformation, and so is the role of the Contract Development and Manufacturing Organization (CDMO).

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Optimizing Your API Partnership: What to Discuss with Your CDMO
CDMO

Optimizing Your API Partnership: What to Discuss with Your CDMO

In the fast-paced and highly regulated world of pharmaceuticals, partnering with the right CDMO partner can be a defining factor in the success of your small molecule API project.

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Explore our related services

Browse through our related services that complement your needs and provide comprehensive solutions.

Active Pharmaceutical Ingredients

Supplying high-quality APIs tailored to your pharmaceutical formulations.

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Intermediates

Offering a range of advance intermediates crucial for pharmaceutical synthesis.

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Intermediates

mRNA Vaccine Ingredients

Providing essential components for vaccine manufacturing.

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mRNA Vaccine Ingredients
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