News

SSI Diagnostica Group Acquires Breath Test Maker Gulf Coast Scientific

Infectious disease diagnostics firm SSI Diagnostica Group said on Thursday that it has acquired Florida-based breath testing firm Gulf Coast Scientific for an undisclosed sum.

Gulf Coast Scientific is a developer of urea breath tests for Helicobacter pylori infection, which is associated with conditions including chronic gastritis and gastric cancer. SSID Group said that the acquired assets will be complementary to its gastric health portfolio and will let SSI offer a broader range of specialized products to US reference and hospital labs.

Financial and other terms of the deal were not disclosed.

Denmark-based SSID Group is a developer of infectious disease tests and antisera as well as reagents for gastric, respiratory, and blood-borne diseases and has facilities in California and Virginia. With the Gulf Coast Scientific acquisition, the company expects to generate revenues of DKK 850 million ($129.5 million) and deliver market-beating growth.

Nachum Shamir, SSID Group’s chair of the board of directors, said in a statement that the acquisition demonstrates a commitment to investing into and building the company.

“Our goal for the next few years is to rapidly grow SSID Group organically and through acquisitions,” Shamir said. “The USA is a key market, and we are excited to strengthen our position further with additional synergistic quality products in a new technological area.”

SSID Group CEO Christina Lindved added that customers in the US prefer to use a combination of rapid antigen-based screening and urea breath testing for H. pylori to provide testing for patients with differing sampling needs, and the acquisition allows the company to meet customer needs and serve more patients.

 

Read more here.

Recent News

08/25/2026

United Therapeutics Corporation Announces FDA Filing Acceptance of New Drug Application for Ralinepag to Treat Pulmonary Arterial Hypertension

United Therapeutics Corporation (Nasdaq: UTHR), a public benefit corporation, today announced that the FDA has accepted the New Drug Application (NDA) for ralinepag to treat PAH. The FDA has set a Prescription Drug User Fee Act target action date of June 24, 2027. Ralinepag has not been approved for use in any indication by the

08/19/2026

ATCC Receives New CDC Award to Advance Influenza Testing and Surveillance

ATCC has been selected by the Centers for Disease Control and Prevention (CDC) for a new contract to support serological assays for the detection and characterization of influenza viruses. The award, valued at up to $7.3 million over the 5-year contract period (contract 75D30126C21030), will support CDC’s National Center for Immunization and Respiratory Diseases, Influenza

08/18/2026

Nanochon Receives Regulatory Approval from Panamá’s Ministry of Health to Initiate First-in-Human Clinical Study of Chondrograft™

Nanochon, a medical device company developing Chondrograft™, a novel patented implant for the treatment of articular cartilage defects of the knee, today announced that it has received regulatory approval from Panamá’s Ministry of Health to initiate its First-in-Human (FIH) clinical study in Panamá. The study will evaluate the safety and performance of Chondrograft™ in patients