CDMO Services
Your Strategic Partner in Pharmaceutical Development and Manufacturing
At Chemox Pharma Pvt. Ltd., we are dedicated to transforming innovative pharmaceutical concepts into reality. As a premier Contract Development and Manufacturing Organization (CDMO),we procide comprehensive, integrated development and manufacturing services under one roof; that empower pharmaceutical companies to bring groundbreaking products to market with speed, precision, and regulatory excellence.
With a focus on quality, reliability, and cutting-edge technologies, we help you navigate the complex landscape of drug development, clinical trials, and commercial manufacturing – ensuring that our products reaches its full potential safely, efficiently, and cost-effectively.
Our Expertise:
- Comprehensive Drug Development Services
- Scalable Commercial Manufacturing Solutions
- Full Regulatory Affairs & Compliance Support
- Customized Packaging & Global Supply Chain Management
Partner with Chemox Pharma for a seamless and successful journey from concept to commercialization. Let’s accelerate your success together!
Why Chemox Pharma?
Tailored Drug Development
From KSM to final API product, we specialize in developing the right molecule for your therapeutic target.
Analytical & Stability Studies
Ensure the quality, stability, and safety of your drug through rigorous testing and optimization.
Technology Transfer
Smooth, efficient transfer of manufacturing processes to commercial-scale production.
Commercial Manufacturing
High-volume manufacturing capabilities, offering flexibility in batch sizes and packaging, with on-time delivery to global markets.
Regulatory Submission Support
Expert guidance through global regulatory landscapes (FDA) to ensure smooth market access.
Compliance Excellence
Adherence to GMP, GLP, and other global standards to guarantee product safety and efficacy.
Audit & Documentation Services
Comprehensive support in regulatory documentation, submissions, and audit preparation.
Innovative Packaging Solutions
Custom packaging designed to meet your product’s specifications and market needs.
Serialization & Traceability
Compliant serialization services to ensure full traceability and meet global regulations.
Global Supply Chain Expertise
Efficient distribution, logistics, and inventory management for timely and cost-effective global delivery.
Questions you may have?
Find answers to the most commonly asked questions about our services.
What is the typical timeline for a CDMO project with SCL Lifesciences?
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.
Do you offer both small-scale and large-scale manufacturing?
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.
Ready to discuss your needs with us?
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