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AdhexPharma's Comprehensive Contract Development Services

Written by Justine Donzel | Aug 19, 2024 1:55:30 PM

Introduction

AdhexPharma and its subsidiary Labtec both stand as leading providers of specialized contract development services, with a primary focus on the development of topical and transdermal patches, as well as oral films. With a legacy spanning over four decades, AdhexPharma has established itself as a reliable partner in the pharmaceutical industry, renowned for its ability to transform innovative drug delivery concepts into commercially viable products. Their deep-rooted expertise, coupled with a commitment to innovation, makes AdhexPharma an essential partner for companies seeking to navigate the complex journey from drug concept to market.

Expertise in Drug Delivery Solutions

AdhexPharma's expertise lies in its comprehensive approach to drug delivery solutions, particularly in the areas of transdermal patches, and oral films. These delivery methods are increasingly preferred due to their ability to enhance patient compliance, reduce systemic side effects, and provide controlled release of APIs. AdhexPharma leverages its extensive knowledge to offer tailored solutions that meet the unique needs of each client, ensuring that every product is optimized for both efficacy and patient comfort.

Comprehensive Development Stages

AdhexPharma’s approach to drug development is methodical and encompasses multiple stages, each crucial in bringing a product from the initial idea to the market.

  1. Feasibility Stage: The development process begins with the feasibility stage, where the experts conduct thorough evaluations to assess the suitability of APIs for various administration routes, such as topical, transdermal, buccal or oral. This stage is critical, as it provides essential data that guides the decision-making process, ensuring that the chosen delivery method is not only effective but also aligned with the product’s intended therapeutic goals.

  2. Product Development: Following feasibility assessment, AdhexPharma engages in a detailed product development process. This involves a step-by-step approach that focuses on optimizing product performance, ensuring stability under various conditions, and preparing the product for clinical trials. The company’s rigorous development protocols are designed to ensure that each product meets the highest standards of quality and is ready for the next phase of its lifecycle.

  3. Clinical Trial Supply Manufacturing: As the product progresses, AdhexPharma takes on the critical role of manufacturing clinical trial supplies. This stage is essential, involving the production of samples that must meet stringent regulatory requirements for use in clinical trials. With extensive experience and expertise, AdhexPharma ensures that all clinical trial materials are produced to the highest standards, thereby safeguarding the integrity and success of the trials.
    A key advantage offered by AdhexPharma and Labtec is the ability to produce clinical trial samples at both pilot and commercial scales, depending on the trial phase. The pilot scale is designed to replicate the parameters of the commercial scale, ensuring seamless transition and consistency throughout the process 

  4. Formulation Transfer: One of the key services offered by AdhexPharma is formulation transfer, which involves the seamless transition of developed formulations to advanced production facilities. This step is vital in ensuring that the product can move from the development stage to large-scale manufacturing without any hitches, preserving the formulation’s integrity and ensuring consistency in the final product.

 

State-of-the-Art Facilities

AdhexPharma’s research and development efforts are supported by its state-of-the-art facilities, particularly its German R&D site at Labtec. Equipped with cutting-edge technology and tools, these facilities operate under current Good Manufacturing Practices (cGMP) and are fully compliant with the regulations set forth by both the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). This advanced infrastructure is designed to support efficient and precise development processes, allowing AdhexPharma to maximize the potential of each product they work on, from initial concept through to final production. In parallel, AdhexPharma has started the construction of a new 8000m2 building in Chenôve (France).

Strategic Partnerships

At the core of AdhexPharma’s business philosophy is a strong emphasis on building lasting, long-term relationships with its clients. The company is committed to working collaboratively, viewing each project as a partnership rather than a mere transaction. By fostering close relationships, AdhexPharma ensures full alignment with its clients’ goals and delivers high-quality, innovative drug delivery solutions that meet the rigorous standards of the global pharmaceutical market. Their team of experts is dedicated to supporting each project from the early stages of development through to commercial production, ensuring a seamless and successful journey for every product.

Why Choose AdhexPharma and Labtec?

Choosing AdhexPharma and Labtec as a partner in drug development comes with numerous advantages:

  • Proven Track Record: With over 40 years of experience in the industry, AdhexPharma and Labtec have a history of successfully bringing complex drug delivery systems to market. Their extensive portfolio of completed projects is a testament to their capability and reliability.

  • Global Reach: AdhexPharma’s operations are not confined to a single region; they have the capacity to manage projects on a global scale. This international presence ensures that their clients have access to broad market opportunities, facilitating the global distribution and success of their products.

  • Regulatory Expertise: Navigating the complex regulatory landscape is a critical aspect of drug development. AdhexPharma possesses deep knowledge of FDA and EMA standards, ensuring that every product they develop complies with these stringent regulatory requirements, thereby smoothing the path to market approval.

Conclusion

AdhexPharma’s contract development services are designed to bring innovative drug delivery solutions to life with the highest degree of precision and efficiency. Their extensive experience, state-of-the-art facilities, and unwavering commitment to fostering strategic partnerships make them an ideal choice for pharmaceutical companies looking to transform their ideas into market-ready products. With a proven track record, global capabilities, and regulatory expertise, AdhexPharma stands out as a trusted partner in the journey from concept to commercialization.