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Ankara, TR · Germantown, MD, US — Pharma · Medical · Cosmetic · Food supplement

5 services

Product research-development and regulatory affairs

From concept to dossier: scientific planning and a submission that meets the rules

Taking a product from concept to authorization means planning the science and the regulation at the same table. We handle product-specific decisions together with the requirements of the submission dossier and remove unforeseen costs from the start.

Image · R&D / regulatory affairs

5 services

Science and regulation, on one platform

An experienced team follows your product through the safety and market-access stages as well. A decision made at authorization stays defensible in the reimbursement dossier.

  1. 01.1

    R&D / product-development studies

    Design, planning, execution and reporting of formulation, bioequivalence and drug-development studies. Projects are detailed to include GMP prioritization and clinical / non-clinical reports

  2. 01.2

    Authorization and approval dossiers

    Dossier preparation in CTD format, submission management and follow-up of authority correspondence

  3. 01.3

    SmPC & PL preparation, clinical / non-clinical reports

    Preparation and revision of the Summary of Product Characteristics and Package Leaflet in line with current guidelines

  4. 01.4

    Medical device consulting

    Consulting on medical-device classification, FDA submissions (510(k), De Novo, PMA, Pre-Sub, IDE) and EU MDR technical-file processes

  5. 01.5

    Scientific publication review, writing and medical-writing consulting

    Clinical and non-clinical reports, scientific publications and technical documents (white papers)

  6. 01.6

    Food supplements

    Ingredient assessment, label and claim compliance, application dossier and approval processes in Türkiye and the USA

Let’s plan your dossier together

Tell us what stage your product is at and we will come back with a scope and timeline.

Services