Research & Development
Centre of Excellence: Supporting Innovation at Scale
Our R&D Centre of Excellence is fully integrated with our manufacturing operations, which include 5 plants capable of handling production from 0.5 kg to 2mT, ensuring a seamless transition from development to commercial production. This ensures that we can deliver both innovative and scalable solutions to meet global demands. Our manufacturing facility is accredited with multiple Indian and international accolades like USFDA, EU-GMP, PMDA, WHO-GMP, EcoVadis, ISO 45001, ISO 14001, ISO 9001.
Key features of our Centre of Excellence include:
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State-of-the-art laboratories designed for APIs, Intermediates, and Specialty Chemical synthesis.
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Advanced technologies, including Continuous Flow Reactors, HVD Systems, and Column Purification Techniques.
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Integration with our manufacturing facility, capacities ranging from 0.5 kg to 2mT.
Comprehensive R&D Capabilities
Our R&D facility supports CRO and CDMO projects through a wide range of services critical to pharmaceutical development. Our key R&D services include:
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Process Development & Route Optimization
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Safety & Hazard Assessments
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Stability Studies
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Cleaning Validation
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Regulatory Support
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Process Scale-Up & Validation
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Method Development & Validation
At the Centre, we also utilize the latest software tools such as Scifinder, Cortellis, Sci-Hub, Espacenet, and CAS Ultra for literature searches and GTI assessments, to stay at the forefront of scientific advancements.
Scalable Solutions for Global Compliance
Medilux is fully committed to compliance with global regulatory standards, ensuring that our processes meet the highest international requirements. Our manufacturing facility and R&D operations are designed to provide scalable, cost-effective solutions without compromising on quality. As a CRO, CMO, CDMO, we work with clients to deliver high-quality pharmaceutical products.
Supporting Manufacturing Facilities
Our manufacturing facility, accredited by USFDA, EU-GMP, PMDA, WHO-GMP, EcoVadis, ISO 45001, ISO 14001, ISO 9001, is fully equipped with cutting-edge technologies and infrastructure, including:
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2 API and 3 Intermediate dedicated Manufacturing Plants
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Central Packaging Area
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State-of-the-art warehouse
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Quality Control (QC) and Microbiology Departments
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Effluent Treatment Plant (ETP)
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Quality Assurance (QA) Department
These facilities complement our Centre of Excellence, ensuring that all stages from development to production are integrated and compliant with industry standards.
Key Achievement:
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Years of Experience: Over 30 years of expertise in the pharmaceutical industry.
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Manufacturing Capacity: From 0.5 kg to 2mT, supporting a wide range of production scales across 5 plants.
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Successful Projects: Over 100 contracts and projects completed with success.
OUR OTHER CAPABILITIES
Seamlessly aligning drug development with global regulatory standards and approvals.
Regulatory Affairs
Quality by Design guides everything we do, ensuring consistency and compliance.
Quality Assurance & Control
A robust, integrated approach keeps your supply secure and efficient.
Supply Chain Management
Structured planning, smart resourcing, and precise oversight keep projects on track.
Project Management
Protecting innovation while navigating complex pharmaceutical regulations.
