Contract Development of Finished Drug Products

In the field of Contract Development of FDFs, Midas offers „one stop shop“ solutions with comprehensive management of all project phases. We assess the feasibility of the product candidate and manage the development, IP protection, registration as well as the supply of the finished product ready for marketing.

Added Value by Experience 

Midas is able to support with modular services already in the ideation phase of the Contract Development of Finished Drug Products (FDFs). In doing so, we see ourselves as a partner dedicated to contribute its experience and experts when it is about developing ideas to generate potential and suitable candidates. After an initial assessment of such candidates, Midas supports you in the selection procedure and transfers the most promising option into the definition of first target product profiles.

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Contract Development of finished drug products
*Product Life Cycle Management ideas or attractive portfolio extensions, developed jointly with customer / Contract Development of FDFs

Learn more about the individual project phases in the Contract Development of Finished Drug Products: 

  • Step 1: Idea Phase

    Feasibility Assessment:

    Midas evaluates whether the intended product can be realized from a technical, regulatory and commercial point of view:

    • Commercial analysis (competitiveness, API sourcing, ...)
    • Check of regulatory requirements
    • Evaluation of technical hurdles
    • First estimation of development costs & time

    IP Analysis

    • “Freedom to operate“ patent report
    • First evaluation of potential for relevant own IP claims
  • Step 2: Development Phase
    • Midas is not bound by the limitations in technical eligibility or scale of own equipment. Midas’ experts select the most suitable CDMO as per individual project requirements (technical and commercial eligibility as well as reliability).
    • Assessment of costs and time required to realize the product opportunity: Midas will provide a detailed quotation, which will make all necessary project steps easy to understand and to follow-up.
    • Qualification of development & manufacturing sites
    • Audits of GMP relevant sites (API and FDF)
    • Securing customer interests by taking care of negotiating all relevant contracts
    • Comprehensive project management: from definition and systematic testing of critical parameters (quality by design) to guiding and monitoring all development work
    • Regular review of all data/documents intended for registration (regulatory compliance check)
    • Constant IP monitoring, assessment and filing of potential own IP claims
  • Step 3: Registration Phase
    • Advising on choice of procedure and related authority
    • Preparing and arranging pre-submission/scientific advice meetings with regulatory agencies on behalf of customer
    • Dossier preparation and submission
    • Acting as applicant, taking care of required administrative steps and authority demands (incl. Pharmacovigilance)
  • Step 4: Commercialization
    • Manufacturing & Supply
    • Ensuring timely availability of API and all materials needed for production in batch sizes according to marketing requirements
    • Primary packaging solutions potentially enabling superior stability
    • Order management & Launch preparation
    • Reliable supplies: ensuring that ordered products will be available in time as well as in the right quality and quantity

Your Contact

Andreas Kahm

Andreas Kahm

Business Development
Senior Manager

Midas Pharma GmbH
Rheinstr. 49
55218 Ingelheim

Business Development & Licensing Support

With decades of experience in pharmaceutical licensing we support you to make your projects a success.

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