What We Do
Through our collective knowledge and expertise from pharmaceutical drug research to manufacturing & supply, Vellagen aspires to deliver high quality medicines serving every patient’s need, acute or chronic.
Research & Development
Research & Development is fundamental requirement for enabling healthcare innovations and development of products, processes and analytical methods. Vellagen experts have the knowledge, expertise and scientific acumen to convert materials to medicines swiftly.
Contract Research
Research is expensive and a critical part in a product’s lifecycle. Vellagen enables speed up research through collaboration and let the partners focus on maximizing every product’s potential from manufacturing to market.
Technology Development
Pharmaceutical product and process development involves numerous technologies and techniques to convert materials to medicines using smart and agile scientific approaches. Vellagen team advises on the best and the most effective and efficient ways to achieve speed to market.
Process Development
Process matters the most when it comes to converting materials to medicines using science, technology and people. Vellagen excels in this space with its expertise and collaborates with industry’s leading partners, driving for speed and quality without compromising compliance.
Product Development
Pharmaceutical product development from scratch requires immense efforts. Vellagen team possess over 100 years of cumulative experience of its capable team to develop high value medicinal products, meeting international regulatory and quality standards.
Product Compliance
Compliance to international quality standards and regulatory requirements are the keys to any pharmaceutical product’s success. Vellagen has the right panel of experts with multinational work experiences and working relationships with health authorities to bring medicines to markets with quality, compliance and speed.
Key Differentiators:
What Sets Us Apart
- Vast knowledge and expertise
- Exhaustive library of intellectual property
- Expertise in niche drug formulations
- End-to-end drug development support
- Strong regulatory expertise for efficient approvals
- Focus on speed, quality, safety, and compliance
- Seamless technology and knowledge transfer