About us
OUR MISSION
We combine our experience with assignments for companies, running from global manufacturers to drawing board start-ups, to set up adherence in a way that support your strategy.
With technological developments advancing and legal requirements trying to catch up, there is room to integrate these (changing) requirements with your strategy. After all, both wish to ensure quick access to high quality and safe medical technology. Innovative healthcare technology developers should not be held back by (lagging) legislation, but lead the way in implementation of these changing requirements and thus set the standard.
NAALA can help you in this. We do not leave you with a standard overview of requirements that might be applicable or an endless legal analysis with a two sentence conclusion in unclear jargon. We will have a proper discussion with you and define, together with you, what suits your organization and, above all, how to ensure this efficiently and sustainably to support (and not limit) the daily activities.
“We understand you are not only the manufacturer of a medical device, but also data provider and responsible for information security. Let us help you integrate these strategies and requirements. “
We understand you are not only the manufacturer of a medical device, but also data provider and responsible for information security. Let us help you integrate these strategies and requirements.
Combining our legal and economic backgrounds, we will not just make you comply with current requirements, but build a sustainable compliant strategy. Let’s jointly make your product or service accessible and trustworthy to your target audience.
Anne Sophie Dil, LL.M. | CIPP/E RAC
Anne Sophie has a background in health technology and law. In both the legal profession and during her work at a big four firm, she learned that technological advancements move faster than the law. This reinforced her belief that laws and rules should not be interpreted the same for every organization and that the law should not be restrictive, but rather supportive of innovative companies. A philosophy that she is able to share through NAALA.
Anne Sophie approaches each client question as an individual case and combines this with in-depth legal knowledge to find the appropriate solutions.
+31 (0)6 23 99 54 38
annesophie@naala.nl
Amy Eikelenboom, MSc | CIPP/E RAC
Amy has a background in health economics, policy and law. Working in legal advisory at a big four firm, she shared the belief that legal compliance is intertwined with the commercial strategy of a company and influenced by economical and political factors. Additionally, she learned that demonstrating compliance has the potential to facilitate trust in patients and potential clients, which can have a beneficial impact on the adoption of innovative products. An approach she can fully deploy through NAALA.
Amy will combine legal and regulatory compliance with developments in health policy and economics to provide complete advice.
+31 (0)6 50 05 52 08
amy@naala.nl
annesophie@naala.nl
amy@naala.nl
+31 (0)6 23 99 54 38
+31 (0)6 50 05 52 08
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