Due Diligences

AGINKO experts can be hired to assess various technologies and their market potential. Frequently we have been included in due diligence teams in cases of a merger of acquisition for orthopedic technologies/compounds.


Strategy, Analysis, and Development  

  • Predicate landscape and device design
  • Balancing indication costs and claims
  • Leveraging regulations, competition, and new opportunities


Benefits of AGINKO Consulting

  • Fast and efficient through clean targeting
  • Independence and objectivity as 3rd party consultants
  • Highly experienced technical consultants
  • Deep operational experience
  • Ability to rapidly mobilize and deploy the Technical DD team

Typical Scope  

TDD typically includes an assessment of Medical devices or Drugs in the field of Joint Disease. Our focus makes the difference compared to generalist TDD consultant. We bring market knowledge.

We conduct also DD on an acquisition of Healthcare Providers.
This is achieved through a closely managed process of focused, rapid data collection and assessment of the installed assets, systems, people, and practices.

Regulatory Know How

We specialize in helping medical device companies, pharmaceutical companies, and healthcare institutions comply with international regulations. As a result, we are extremely familiar with the following medical device regulations and can perform audits to determine the extent of compliance with:


  • USA - US Food and Drug Administration regulations
  • Europe - Medical Devices Directives and CE Marking
  • Japan, China, and South Africa
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AGINKO Research AG
AGINKO Research AG, Route de l’ancienne Papeterie 106
1723 Marly
AGINKO Research AG, Route de l’ancienne Papeterie 106
1723 Marly