Pharma Marketing Network

APRIL 10, 2025

With platforms like Bing, LinkedIn, and programmatic networks, pharma marketers can scale efforts across search engines and display placements. For more insights into how top pharma companies are adapting to digital-first strategies, check the latest insights on Pharma Marketing Network. Moreover, PPC isnt just about Google Ads.

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Legacy MEDSearch

FEBRUARY 8, 2023

market with a breakthrough FDA-Class II medical device, TargetCool. ” TargetCool was created by award-winning South Korean mechanical engineer, Dr. Gun-Ho Kim, who specializes in thermal engineering. Recens, Inc. “We truly believe that TargetCool will change the face of cooling,” Dr. Kim stated. Are you hiring?

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Pharma Marketing Network

MARCH 5, 2025

So how can pharma brands maximize their return on investment (ROI) while ensuring compliance with FDA and HIPAA regulations ? The answer is simple search engines and social platforms are where patients and HCPs find information. Partner with verified healthcare ad networks to ensure ads appear on trusted HCP-only platforms.

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Pharma Marketing Network

MARCH 16, 2025

They must be highly targeted, compliant with FDA and HIPAA guidelines, and designed to generate meaningful interactions rather than just impressions. For additional insights on pharma digital marketing, visit Pharma Marketing Network. For advanced tracking insights, visit Pharma Marketing Network. Call-to-action (CTA) buttons.

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Media Pharma Networking Education 52

Legacy MEDSearch

JANUARY 10, 2023

a commercial-stage healthcare business dedicated to neonatal intensive care and the acute care hospital community, announced FDA approval of the newest generation of its tankless inhaled nitric oxide (iNO) delivery system. . Food and Drug Administration (FDA). VERO Biotech Inc., About GENOSYL ® DS. VERO Biotech Inc. Are you hiring?

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Legacy MEDSearch

AUGUST 15, 2022

This is a crucial first step in our path to make the Maestro Brain Model the ‘engine’ in our navigation system supporting multiple new applications in the future. The ClearPoint® Neuro Navigation System has FDA clearance, is CE-marked, and is installed in over 60 active sites in the United States, Canada, and Europe. Are you hiring?

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FDA Recruitment Safety Patients 98

Legacy MEDSearch

FEBRUARY 13, 2023

the groundbreaking medical device company that created the Swoop® system, the world’s first FDA-cleared portable magnetic resonance imaging (MRI) device for imaging of the brain, today announced the U.S. Food and Drug Administration (FDA) 510(k) clearance and launch of the company’s upgraded AI-powered software. Hyperfine, Inc.,

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Food and Drug Administration FDA Recruitment Food 98

European Pharmaceutical Review

AUGUST 1, 2022

The DDiCT project will be co-led by Bristol Myers Squibb (BMS)’s Disability Advancement Workplace Network (DAWN) and the Global Drug Development Team. The US Food and Drug Administration (FDA) recently published a new draft guidance to support companies in enrolling more ethnically diverse trial populations. .

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Legacy MEDSearch

AUGUST 22, 2022

Food and Drug Administration (FDA) has granted 510(k) clearance to the MedWand,” shared MedWand CEO and Co-Founder, Robert Rose. “As With FDA clearance, clinicians and patients everywhere can trust MedWand’s vitals and remote examination tools, and experience telemedicine on an entirely new level.” MedWand Solutions, Inc.

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Legacy MEDSearch

NOVEMBER 29, 2022

engine acts as a second reader to radiological technologists at point-of-care for image quality on every mammogram. Over the past 17 years, we have built one of the strongest networks of device professionals ranging from sales, marketing, research & , quality & regulatory, project management, field service, and clinical affairs.

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Legacy MEDSearch

NOVEMBER 2, 2023

Food and Drug Administration (FDA) to market the SOLACE Sacroiliac Fixation System with proprietary NANOACTIV surface technology and compatibility with StealthStation ® Navigation. The NANOACTIV implant surface demonstrates elements to be considered a nanotechnology as outlined in FDA nanotechnology guidance document.

Medical 52

Medical FDA Food and Drug Administration Recruitment 52

Legacy MEDSearch

JUNE 30, 2023

Food and Drug Administration (“FDA”) for Cresilon Hemostatic Gel (“CHG ”). This marks Cresilon’s first FDA clearance for human use, validating its revolutionary hemostatic gel technology and the company’s global mission to transform wound care. .” Cresilon’s mission is to save lives.

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FDA Food and Drug Administration Recruitment Medical 52

Legacy MEDSearch

SEPTEMBER 11, 2023

Zeta’s computer vision engine ensures maintained accuracy by automatically registering multiple times a second, accounting for patient movement. The post Zeta Surgical’s Mixed Reality Navigation System Receives FDA Clearance appeared first on Legacy MedSearch | Medical Device Recruiters. Are you hiring?

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FDA Food and Drug Administration Recruitment Medical 52

Legacy MEDSearch

JULY 27, 2022

Rapid Medical , a leading developer of advanced neurovascular devices, announces FDA 510(k) clearance for TIGERTRIEVER 13 for large vessel occlusions at the 2022 Society of NeuroInterventional Surgery’s (SNIS) 19th Annual Meeting in Toronto. TIGERTRIEVER 17 and 21, COMANECI , and COLUMBUS /DRIVEWIRE are CE marked and FDA cleared.

Medical 52

Medical FDA Recruitment Physicians 52

Legacy MEDSearch

JUNE 14, 2022

Xenco Medical has expanded its ASC surgical device portfolio through the FDA clearance and launch of its Multilevel CerviKit , an expansion of Xenco Medical’s breakthrough single-use cervical spine technology to include a comprehensive suite of implants and single-use instruments for 2, 3, and 4 level anterior cervical spine procedures.

Medical 52

Medical FDA Recruitment Engineering 52

Legacy MEDSearch

JULY 31, 2023

Axial3D, a leader in medical segmentation and 3D solutions, today announced that it is the first to receive FDA clearance for an automated, AI-driven, cloud-based segmentation platform for orthopedic trauma, orthopedic, maxillofacial, and cardiovascular applications.

Medical 52

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Legacy MEDSearch

JUNE 19, 2023

The FDA approval is significant as it recognizes the safety and effectiveness of iTFlow® in analyzing blood flow through 4D Flow MRI data, with the potential to enhance diagnostic accuracy for patients with cardiovascular diseases and heart conditions. The US Food and Drug Administration has approved the use of iTFlow® in blood flow analysis.

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FDA Food and Drug Administration Recruitment Physicians 52

Legacy MEDSearch

MAY 30, 2023

Food and Drug Administration (FDA). About Sagentia Innovation Sagentia Innovation is a science and engineering R&D consultancy based in Cambridge, U.K. The post THINK Surgical Receives FDA 510(k) Clearance for TMINI Miniature Robotic System appeared first on Legacy MedSearch | Medical Device Recruiters. Are you hiring?

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Legacy MEDSearch

JUNE 14, 2023

Food and Drug Administration (FDA) 510(k) clearance for its Pounce LP (Low Profile) Thrombectomy System. Surmodics also develops and commercializes highly differentiated vascular intervention medical devices that are designed to address unmet clinical needs and engineered to the most demanding requirements. Surmodics, Inc.

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FDA Food and Drug Administration Recruitment Medical 52

Pharma Marketing Network

MARCH 20, 2025

Develop an Omnichannel Strategy : Integrating multiple touchpoints, including social media, programmatic advertising, email marketing, and search engine optimization (SEO), helps maintain a consistent brand presence. For more expert insights, visit Pharma Marketing Network. Why is healthcare marketing changing so rapidly?

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Legacy MEDSearch

SEPTEMBER 29, 2023

Obtaining IDE Approval for the HYDRAFIL-D Study from the FDA is a major milestone for ReGelTec,” said Bill Niland, the company’s co-founder and CEO who has successfully founded and exited multiple healthcare companies including Harpoon Medical, Inc., Vapotherm (NYSE:VAPO), and National Sleep Technologies. ABOUT REGELTEC, INC: ReGelTec, Inc.

FDA 52

FDA Food and Drug Administration Recruitment Medical 52

Legacy MEDSearch

SEPTEMBER 1, 2022

eCential Robotics, a French growth MedTech company that designs and produces a system unifying 2D/3D imaging, surgical navigation and robotics, announced FDA 510(k) clearance of its 3D imaging, navigation and robotics guidance system, securing the penetration of its unified robotic platform in the United States. Securing the U.S.

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FDA Recruitment Marketing Medical 52

Legacy MEDSearch

APRIL 7, 2023

Food and Drug Administration (FDA) has granted 510(k) clearance to the Axiom PSR System for use with the company’s Kinos Axiom Total Ankle System. The convergence of our inhouse 3d printing capabilities, advanced engineering, and clinically focused research teams allows us to provide the next generation patient-specific devices.

Patients 52

Patients FDA Food and Drug Administration Recruitment 52

Legacy MEDSearch

APRIL 14, 2023

Northwell Holdings, the venture investment arm of Northwell Health, Topspin Fund, and Long Island Angel Network also participated in the round. This funding will be used by Neuvotion to further expand its team, complete clinical studies, and obtain FDA clearance for its initial product. ” About Neuvotion, Inc. (IPS)

Engineering 52

Engineering Networking Recruitment Medical 52

PM360

NOVEMBER 27, 2023

If a misinterpretation exists between engineers and testers on the solution developed, then such requirements will have higher risks on the entire lifecycle. AI/ML technologies offer a streamlined approach by creating health alert monitors that analyze event triggers, database usage, and network alerts.

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Engineering Medical science Healthcare Provider Healthcare 115

Legacy MEDSearch

FEBRUARY 3, 2023

a commercial-stage healthcare business dedicated to neonatal intensive care and the acute care hospital community, announced FDA approval of its innovative second generation GENOSYL® Inhaled Nitric Oxide (iNO) delivery system for use with rebreathing anesthesia in the operating room setting. Food and Drug Administration (FDA).

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FDA Food and Drug Administration Recruitment Patients 52

Pharmaceutical Technology

JUNE 5, 2023

The attackers use various tactics to gain unauthorised access to a computer system, network, or device with the intention of stealing, modifying, or destroying data for strategic or financial gain. Social engineering attacks will rise, in addition to phishing, smishing and deepfake attacks.

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Legacy MEDSearch

JANUARY 4, 2023

Food and Drug Administration (FDA) 510(k) clearance of its Zoom RDL Radial Access System, the company’s latest innovation in elevating stroke care and the first radial access platform developed specifically for ischemic stroke treatment. Imperative Care, Inc., announced U.S. 088” lumen for compatibility with large-bore aspiration catheters.

FDA 52

FDA Food and Drug Administration Physicians Recruitment 52

Legacy MEDSearch

FEBRUARY 21, 2024

In June 2023, Sparrow received FDA clearance for the downloadable application, making it the first FDA-cleared smartphone stethoscope software-as-a-medical-device (SaMD). The company later obtained additional FDA clearance for consumer use, empowering individuals to actively monitor their heart health.

Medical 52

Medical FDA Recruitment Engineering 52

Pharma Marketing Network

FEBRUARY 27, 2025

For pharma marketers, PPC campaigns typically fall into three main categories: Search Ads: Appear on search engines when users look for specific keywords (e.g., While pharma brands should invest in search engine optimization (SEO) for sustained growth , PPC ensures immediate traffic to branded websites, drug pages, and lead-generation forms.

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Pharma Marketing Networking Prescription 52

Legacy MEDSearch

MAY 9, 2023

Webster, III, PhD also co-founded the Vanderbilt Institute for Surgery and Engineering (VISE) with Dr. Duke Herrell. They developed the Virtuoso Surgical system with a design team helmed by COO and Lead Engineer Richard Hendrick, PhD. This device has not yet been approved by the FDA and is not for sale in the United States.

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Recruitment Engineering Sales Medical 52

Pharma Marketing Network

OCTOBER 29, 2024

Leveraging Search Engine Optimization (SEO) Optimizing your website and content for search engines is essential to rank higher in search results. Emphasizing Compliance and Ethical Standards Maintaining compliance with regulatory bodies like the FDA is crucial in healthcare marketing. How does SEO benefit healthcare brands?

Healthcare 52

Healthcare Healthcare Marketing Pharma 52

European Pharmaceutical Review

MARCH 12, 2024

Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. Blockchain technology creates a decentralised and unalterable ledger that records all transactions across a network of computers.

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Government Pharma Training Ethics 98

European Pharmaceutical Review

AUGUST 31, 2023

However, companies must not only use their logistical know-how to knit well-functioning infrastructure networks but also adhere to standards that consider environmental and patient safety. FDA approves new treatment for certain digestive tract cancers [Internet]. Pluvicto [Internet]. ema.europa.eu [cited 2023 May].

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Food and Drug Administration Manufacturing Safety Transportation 97

Legacy MEDSearch

APRIL 5, 2023

announced today that the FDA has granted premarket approval (PMA) of the NeuRx ® Diaphragm Pacing System (NeuRx DPS ® ) for use in patients with spinal cord injuries who rely on mechanical ventilation. PMA is the most stringent type of device marketing application required by FDA. Synapse Biomedical, Inc.

Patients 52

Patients Recruitment FDA Medical 52

PM360

NOVEMBER 29, 2022

1 And, on average , the FDA approved 60% more drugs between 2010-2019 than the yearly average over the previous decade. If you apply the right AI engines, you will get increasingly better insights. It’s a lot of balls to keep up in the air—and often without the right technology support.

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Medical science Medical Customer Relationship Management Doctors 95

pharmaphorum

NOVEMBER 7, 2022

Since Mitch helped to found Aerie as a Duke University spinout in 2005, Aerie has filed 5 INDs and 2 NDAs, with its first FDA approval coming in 2017 and Najam (Naj) Sharif, PhD, DSc (Southampton University, UK) has >34-years’ pharmaceutical drug discovery research/development experience covering neuroscience and ophthalmology.

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