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Intellectual Property

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IPR Expertise at Medilux

Medilux is committed to protecting intellectual property and ensuring compliance in the highly regulated pharmaceutical industry. Our team of experienced scientists and legal professionals is dedicated to adding capabilities to APIs and ensuring that our IPR activities comply with all relevant laws and regulations. We are constantly developing innovative technologies to stay ahead in the industry.

Key Services Include:

  • IP Portfolio Management: Developing and maintaining a comprehensive IP portfolio to protect innovations.
     

  • IP Valuation: Evaluating the commercial value of our IP assets.
     

  • IP Licensing & Collaboration: Managing licensing agreements and collaborations.
     

  • Third-Party Collaboration: Open to IP collaborations with partners and third parties.
     

  • Early Involvement: Engaging with R&D teams early to identify potential IP assets.
     

  • IP Strategy: Crafting IP strategies to support business objectives.
     

  • Non-Infringing Routes: Identifying and developing non-infringing API manufacturing routes.
     

  • IP Queries: Addressing IP-related queries with clear, satisfactory solutions.

Our Dedicated IP Team

We have a team of IP attorneys and professionals specialized in science and IP law who ensure that Medilux’s IP wealth is well protected. With a focus on innovation and compliance, we are dedicated to safeguarding both our own and our partners' intellectual property.

OUR OTHER CAPABILITIES

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Advanced reactions executed safely, efficiently, and at scale.

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Chemistry and Reactions

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From molecule to market, our Centre of Excellence links discovery with scalable production.

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Research & Development

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Quality by Design guides everything we do, ensuring consistency and compliance.

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Quality Assurance & Control

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A robust, integrated approach keeps your supply secure and efficient.

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Supply Chain Management

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Structured planning, smart resourcing, and precise oversight keep projects on track.

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Project Management

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Seamlessly aligning drug development with global regulatory standards and approvals.

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Regulatory Affairs

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