Inter Scientific Supports the EU Certification for First Handheld Liquid Inhalation Device

Inter Scientific is pleased to announce its role, in collaboration with Jupiter Research LLC, as the regulatory partner for the first handheld Liquid Inhalation Device to receive regulatory approval under Regulation (EU) 2017/745 (EU MDR). This regulatory milestone marks a significant step forward in the medical device landscape and opens the door for wider global access to innovative inhalation technologies.

Jupiter Research, a pioneering company in the liquid vaporizer space, identified early in its development journey the importance of an expert regulatory partner. After an initial review process, Jupiter selected Inter Scientific based on its ability to meet the demands and complexity of the EU MDR. This decision proved instrumental in Jupiter’s successful regulatory approval.

“Jupiter recognised very early in the process that external support would be beneficial,” stated Jupiter’s Senior Director of Engineering, Jordan Walker. “We chose Inter Scientific based on their expertise and felt they were efficient and professional throughout the contract, helping us achieve our goals and gain regulatory approval.”

Walker continued, “Inter Scientific provided expertise in the creation of the device’s comprehensive Technical File, development of the required Quality Management System documentation, and delivery of tailored educational services to Jupiter’s internal teams. This approach enabled a streamlined path to regulatory compliance.”

David Lawson, Executive Director at Inter Scientific, commented:
“At every stage of this rigorous certification process, Inter Scientific maintained a customer-focused approach, working closely with the Jupiter team and delivering timely, professional, and accurate support. We’re proud to be recognised as a key contributor to this success and look forward to building on this achievement through continued collaboration on future regulatory initiatives.”

Inter Scientific’s in-depth understanding of the regulatory framework helped Jupiter design the device in line with medical classification requirements, prepare the necessary documentation, and respond effectively to regulatory feedback, which resulted in the successful approval of a first of its kind device now poised to make its mark in global healthcare.

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