df23

Our Services

Our Partnership

Discovering the Power of collaboration

Across Europe, we bring deep expertise in the pharmaceutical industry and a comprehensive understanding of its regulatory landscape. This knowledge empowers us to navigate the development process with precision, accelerating treatments from concept to market.

We are constantly seeking new collaborations and innovative therapies to enhance our portfolio. If you have a potential medication that could make a difference for patients, we are eager to learn more.

Our mission is to drive healthcare innovation. We are dedicated to exploring fresh ideas and building impactful partnerships to deliver transformative solutions to patients across Europe.

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Product Licensing (In and Out)

Product Licensing

In Licensing:

At DF23, licensing plays a key role in expanding our product portfolio and enhancing our offerings in the dynamic pharmaceutical landscape. By collaborating with innovative companies and acquiring rights to promising products, we drive growth and bring advanced treatments to patients. Our strategic approach to product selection ensures a strong pipeline of therapies addressing diverse medical needs across Europe.

Out Licensing:

Our commitment to advancing healthcare extends beyond our portfolio. Through our licensing, we collaborate with like-minded partners to share our expertise and products for the benefit of the global patient population. By licensing our technologies and products, we contribute to the broader medical community and drive innovation across the industry.

Regulatory Affairs services

Regulatory Affairs Consulting in Europe

At DF23, our team of global pharmaceutical experts provides comprehensive support to help you navigate all regulatory aspects of life sciences in Europe, from development and registration to commercialization.

We specialize in providing top-level regulatory affairs consulting services, including CMC, quality assurance, non-clinical studies, toxicology, clinical trials and medicinal product compliance.

Regulatory affairs professionals are a vital bridge between pharmaceutical companies and health authorities. They ensure seamless management of every stage of product development, maintaining transparency and efficiency. Our team ensures regulatory compliance throughout the entire product lifecycle, from early-stage development to final approval and commercialization.

Partner with DF23 to ensure that your pharmaceutical products meet the highest regulatory standards across Europe.

Distribution

Logistics Management

At DF23, our logistics management system ensures efficient and reliable delivery of pharmaceutical products to every corner of the world. By utilizing advanced supply chain technologies, performing rigorous quality checks, and fostering strategic partnerships, we ensure timely and safe deliveries. This commitment enables healthcare providers and patients to access our lifesaving medicines exactly when they are needed most.

Comparator Drug Sourcing (RLD)

Comparator Drug Sourcing (RLD)

At DF23, we specialise in comparator drug sourcing (RLD) in Poland, ensuring high-quality and compliant pharmaceutical products for clinical trials. Our strong network with certified suppliers and manufacturers allows us to provide authentic reference-listed medicines (RLD) at competitive prices, ensuring timely delivery and full regulatory compliance.

Why Choose DF23 for Comparator Drug Sourcing?

  • Global network and regulatory expertise: We understand the regulatory requirements of each region, ensuring compliance and seamless sourcing.
  • Audited and reliable supply chain: We collaborate with validated and traceable suppliers to guarantee product authenticity and quality.
  • Cold chain and special handling for hard-to-source products: Expertise in handling temperature-sensitive drugs, specialty pharmaceuticals, and hospital lines with GDP-compliant storage solutions.
  • End-to-end logistics and compliance: Our secure distribution system ensures timely delivery with advanced packaging solutions such as Credo Box packaging and data loggers.

At DF23, we are committed to providing cost-effective, compliant, and timely comparative drug sourcing to support clinical trials globally.

Our vission-df23

Re-purpose

Repurposing involves taking an existing drug or compound and finding new therapeutic applications beyond its original intended use.

Our vission-df23

Re-engineering

Re-engineering in the pharmaceutical industry refers to the process of increasing the efficiency, quality and cost-effectiveness of various stages of drug development, manufacturing or distribution.

Our vission-df23

Re-formulation

Reformulation involves modifying the structure of a drug to optimize its therapeutic effect, improve patient compliance, or reduce side effects.

Reach Out to Us for Your Pharmaceutical Product Inquiries!

At df23, we prioritize your needs and are committed to providing exceptional support for all your pharmaceutical product inquiries. Our knowledgeable team is available to guide you through our diverse offerings, ensuring you find the right solutions for your healthcare needs.

Whether you need detailed product information, pricing or assistance with ordering, we are just a message or call away. We also welcome potential partners to explore collaborative opportunities, as we believe in building strong, mutually beneficial relationships. Contact us today, and let us help you navigate the world of high-quality pharmaceuticals!

  •  Personalized Solutions for Your Needs
  •  Comprehensive Product Information
  •  Dedicated Customer Support
  •  Long-Term Partnership Commitment

Contact Us

Contact us for inquiries, partnerships, and learn how we can help with your pharmaceutical needs.

    Lets Get in Touch!

    We look forward to connecting with you to meet your pharmaceutical needs and explore opportunities for collaboration. Get in touch today!

    Call us

    +48-695844617

    Email us

    info@df23.pl