In Licensing: In the dynamic pharmaceutical landscape, In Licensing plays a pivotal role in expanding our product portfolio and enhancing our offerings. By partnering with innovative companies and acquiring rights to promising products, we drive growth and bring advanced treatments to patients. Our strategic approach to selecting and licensing products ensures that we maintain a robust pipeline of therapies that cater to diverse medical. needs.
Out Licensing: Our commitment to advancing healthcare goes beyond our own portfolio. Through Out Licensing, we collaborate with like-minded partners to share our expertise and products for the benefit of global patient populations. By licensing our technologies and products, we contribute to the broader medical community and foster innovation across the industry
Our co-development teams are composed of multidisciplinary experts who combine their knowledge and skills to drive breakthrough solutions. By joining forces with researchers, clinicians, and industry partners, we create an environment where diverse perspectives converge to solve complex medical challenges. These cross-functional teams ensure that our projects are nurtured from concept to realization, resulting in impactful advancements that improve the lives of patients around the world.
In a rapidly evolving landscape, the successful transfer of technology is crucial. Our commitment to excellence extends to our collaboration with Contract Manufacturing Organizations (CMOs). We ensure the seamless transition of our formulations and manufacturing protocols through meticulous technology transfer processes. This collaboration enhances our production capabilities, agility, and quality standards, ultimately benefiting patients who rely on our high-quality pharmaceuticals.
Our logistics management ensures that our pharmaceutical products reach every corner of the globe with utmost efficiency and reliability. By leveraging advanced supply chain technologies, rigorous quality checks, and strategic partnerships, we guarantee timely and secure deliveries. This enables healthcare providers and patients to access our life-changing medications when they need them the most.
Re-purposing:Re-purposing involves taking an existing drug or compound and exploring new therapeutic applications beyond its original intended use.
Example: A pharmaceutical company had developed a drug initially intended for treating a specific type of autoimmune disorder. However, during clinical trials, researchers noticed that the drug also had potential anti-inflammatory effects. The company decided to re-purpose the drug and conduct further studies to explore its efficacy in treating a range of inflammatory conditions, such as rheumatoid arthritis and Crohn's disease. This approach allowed the company to tap into new markets and indications without starting from scratch.
Re-engineering:Re-engineering in the pharmaceutical industry refers to the process of enhancing the efficiency, quality, and cost-effectiveness of various stages in drug development, manufacturing, or distribution.
Example: A pharmaceutical manufacturer identified that their existing packaging and labeling processes were inefficient and prone to errors. To address this, they implemented a re-engineering strategy that involved adopting automated packaging equipment, barcoding systems, and quality control checks. This re-engineering effort resulted in reduced packaging errors, improved traceability, and increased overall operational efficiency.
Re-formulation: Re-formulation entails modifying the composition of a drug to optimize its therapeutic effects, improve patient adherence, or reduce side effects.
Example: A pharmaceutical company had a widely used pain medication available in tablet form, but some patients found it difficult to swallow. To enhance patient compliance, the company initiated a re-formulation process. They developed a new formulation of the drug in a liquid suspension form, making it easier for patients who had difficulty swallowing tablets. This re-formulated version improved patient satisfaction and adherence to the prescribed treatment regimen.
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Get in touch to Report Adverse Drug Reactions (ADRs). At Novumgen, the well-being of patients is of the utmost importance. Should you encounter any unanticipated side effects or adverse responses linked to our products, we urge you to get in touch with us promptly. Your insights play a pivotal role in upholding the enduring safety and excellence of our medicinal products. To contact our specialist team for ADR reporting please complete the following:
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India Novumgen Private Limited Lotus Aura-1, LF-18G Sama Savli Road Vadodara, 390024, Gujarat
United Kingdom Novumgen Limited 20-22 Wenlock Road, London, N1 7GU