Legacy MEDSearch

JULY 21, 2023

UroMems , a global company developing innovative, mechatronics technology to treat stress urinary incontinence (SUI), announced today that it has successfully completed the first-ever implant of the UroActive smart, automated artificial urinary sphincter (AUS) in a female patient. Food and Drug Administration).

Food and Drug Administration 52

Food and Drug Administration Patients Safety Recruitment 52

Legacy MEDSearch

DECEMBER 6, 2022

With ActivSight, surgeons can access critical intraoperative visual data as augmented reality overlays, helping to increase surgical outcomes and patient safety. “As We believe ActivSight will be a game-changer in the operating room by revolutionizing surgical vision and, ultimately, improving surgical care and patient safety.

Food and Drug Administration 98

Food and Drug Administration Safety Recruitment Medical 98

Legacy MEDSearch

MARCH 24, 2023

a company developing a completely transcatheter device-based therapy to address heart failure (HF), announced that patients treated with the investigational AccuCinch ® Ventricular Restoration System demonstrated improvement in HF patient outcomes and beneficial changes in the structure of the heart. Ancora Heart, Inc.,

Patients 52

Patients Recruitment Medical Medicine 52

Legacy MEDSearch

SEPTEMBER 26, 2023

This approval applies to all commercially implanted Evoke ® System patients in the United States as well as patients formerly enrolled in the ECAP Study. The approval provides patients implanted with the Evoke ® System the ability to undergo 1.5 IDE study with 300 patients enrolled. head and extremity and 1.5T

Medical 52

Medical FDA Food and Drug Administration Safety 52

Legacy MEDSearch

SEPTEMBER 27, 2022

Food and Drug Administration (FDA) 510(k) clearance for its CellFX System, expanding the indication for use to include the treatment of sebaceous hyperplasia in patients with Fitzpatrick skin types I-III. The clearance was based on clinical data from the Company’s IDE approved study for the treatment of sebaceous hyperplasia. “We

FDA 98

FDA Food and Drug Administration Recruitment Medicine 98

Legacy MEDSearch

JANUARY 13, 2023

Hip Innovation Technology , LLC (HIT), a medical device company developing innovative orthopaedic device solutions to advance the quality of life and quality of care for patients, is pleased to announce the first U.S. Safety will be assessed through the collection of device-related adverse events and patient quality of life metrics.

FDA 98

FDA Safety Recruitment Patients 98

Legacy MEDSearch

AUGUST 15, 2022

This first-generation anatomical segment analysis tool emerged over 10 years ago from research aimed at detecting subtle volumetric and shape abnormalities in patients with mild traumatic brain injury. More importantly, it provides point-based correspondence longitudinally and across patients. About ClearPoint Neuro.

FDA 98

FDA Recruitment Safety Patients 98

Legacy MEDSearch

NOVEMBER 7, 2022

a company committed to advancing surgical efficiency and safety, announced that they have received Safer Technologies Program (STeP) designation from the FDA for their surgical device StimSite. “Surgeons are constantly learning new techniques, either robotics or laparoscopic, and safety is always front and center.

Medical 95

Medical FDA Safety Recruitment 95

Legacy MEDSearch

AUGUST 8, 2022

The SkyWalker System has the technical advantages of precise operation and efficient coordination, while prioritizing safety. Prior to the actual surgery, the planning system assists surgeons in formulating personalized patient implant plans based on preoperative CT scan anatomical data as well as specific implant data.

Food and Drug Administration 98

Food and Drug Administration Recruitment Medical Food 98

MedCepts

NOVEMBER 7, 2017

Selling involves skills and traits which improve the possibilities of getting a sales concluded. The Exceptional Sales Representative and Physician Relationship. Obviously, the product or service itself has to be pass safety and efficiency standards. The Physician and Sales Rep Relationship.

Physicians 52

Physicians Sales Doctors Medical 52

Pharma Marketing Network

AUGUST 9, 2023

Adhere to Labeling and Packaging Requirements The labeling and packaging of pharmaceutical products are tightly regulated to ensure safety and accurate information. Train Your Team Educate your marketing and sales teams about the regulatory landscape and the importance of compliance.

Marketing 52

Marketing Pharma Food and Drug Administration Media 52

Pharma Marketing Network

JANUARY 6, 2021

Tools that help people track their health, including apps, wearables, and patient portals will be used more than ever in 2021. Due to the pandemic, the healthcare industry has gone almost completely virtual Patient visits with HCPs, meetings between HCPs and sales reps, and healthcare conferences have all had to endure the virtual shift.

Marketing 98

Marketing Pharma Media Safety 98

Scott’s Directories

NOVEMBER 22, 2023

As healthcare professionals navigate the complexities of patient care, research, and pharmaceutical advancements, the demand for reliable resources has never been higher. Streamlining New Drug Introductions The path to introducing a new drug is fraught with challenges, from ensuring efficacy and safety to navigating regulatory landscapes.

Medical 52

Medical Healthcare Healthcare Healthcare Provider 52

Rep-Lite

OCTOBER 26, 2023

Why Nurses Choose to Make Career Changes Nursing is a multifaceted field , and after years of delivering hands-on patient care, many nurses yearn for diversification. A Desire for New Challenges Nurses are problem solvers by nature, and many develop a yearning for new challenges that lie beyond the realm of patient care.

Education 52

Education Healthcare Healthcare Recruitment 52

Pharma Marketing Network

JULY 19, 2023

This can help to increase trust and credibility and ultimately drive sales. These platforms can be used to connect with patients and healthcare providers, share educational content, and build relationships. VR can be used to create immersive experiences that allow patients to visualize different medical conditions and treatments.

Marketing 96

Marketing Pharma Media Healthcare Provider 96

Pharma Marketing Network

MAY 15, 2023

One of the biggest opportunities presented by big data in the pharmaceutical industry is the ability to gain insights into patient needs and preferences. One of the biggest challenges is ensuring that patient privacy is protected. However, the use of big data in pharmaceutical marketing also poses significant challenges.

Pharmaceutical 59

Pharmaceutical Marketing Electronics Media 59

Legacy MEDSearch

NOVEMBER 29, 2022

generated image quality assessments while the patient is still in the exam room, and supports reduced technical recalls and improved mammography quality. Densitas ® is a global leader in artificial intelligence solutions for breast cancer screening, focused on quality, safety, efficiency, and precision breast health.

Recruitment 98

Recruitment FDA Engineering Management 98

Legacy MEDSearch

DECEMBER 12, 2022

“Nerivio is an excellent treatment option for our patients with migraine, especially those who do not respond to medications, or cannot tolerate their side effects. .” Dr. Synowiec is the medical lead of this Coverage with Evidence program. See Full Press Release at the Source: Pennsylvania-based Highmark Inc.

Side effects 98

Side effects Insurance FDA Pharmacology 98

Legacy MEDSearch

OCTOBER 9, 2023

Data pooled from both the US and European/UK trials were used to assess the clinical safety and efficacy of histotripsy in destroying targeted primary and secondary liver tumors. Our clients include both blue-chip companies and innovative startups within the MedTech space.

FDA 52

FDA Food and Drug Administration Physicians Safety 52

Legacy MEDSearch

MARCH 20, 2023

(NYSE American: ASXC), a medical device company that is digitizing the interface between the surgeon and the patient to pioneer a new era of Performance-Guided Surgery (PGS), announced that it has received 510(k) clearance from the FDA for an expanded indication to treat pediatric patients with the Senhance® System. Europe, and Japan.

FDA 52

FDA Recruitment Patients Medical 52

Legacy MEDSearch

SEPTEMBER 5, 2023

However, insufficient image guidance precision and treatment control, lead to high risk of recurrence and complications, creating significant barriers to widespread adoption and limiting patients’ eligibility. solution is not yet approved for sale or distribution in the USA and is limited by USA law to investigational use.

FDA 52

FDA Food and Drug Administration Physicians Recruitment 52

PharmaKinnex

AUGUST 23, 2022

From new legislation to functional shifts in marketing and advertising, the pharma industry works hard every day to keep up with new regulatory requirements and the constantly evolving expectations of prescribers and patients. – Inefficient & Expensive Sales Strategies. More convenience and safety? What’s not to love?

Pharma 52

Pharma Sales Sales Strategy Marketing 52

Pharma Marketing Network

OCTOBER 16, 2023

The pharmaceutical industry is increasingly turning to social media to reach patients, healthcare professionals, and other stakeholders. It also provides an opportunity to share valuable information, such as product information, health advice, and safety warnings. Companies should also consider the long-term impact of their campaigns.

Media 52

Media Pharmaceutical Marketing Safety 52

Pharma Marketing Network

MARCH 23, 2023

One of the biggest opportunities presented by big data in the pharmaceutical industry is the ability to gain insights into patient needs and preferences. One of the biggest challenges is ensuring that patient privacy is protected. However, the use of big data in pharmaceutical marketing also poses significant challenges.

Pharmaceutical 52

Pharmaceutical Marketing Electronics Media 52

Legacy MEDSearch

OCTOBER 25, 2023

Theranica , a neuromodulation therapeutics company, announced the publication of a comprehensive clinical study in Advances in Therapy examining the long-term utilization, clinical efficacy, and safety of Nerivio ® , a Remote Electrical Neuromodulation (REN) device for the treatment of migraine. As for clinical efficacy, 74.1%

Side effects 52

Side effects Recruitment Networking Management 52

Legacy MEDSearch

JUNE 27, 2022

This funding will help propel the company into new surgical applications, accelerate its commercial sales and add to its growing clinical evidence repository. He also noted that Centerline is a success story for Northeast Ohio. Our clients include both blue-chip companies and innovative startups within the MedTech space.

Recruitment 52

Recruitment Healthcare Healthcare Safety 52

Infuse Medical

MARCH 22, 2024

Healthcare training is a crucial aspect of maintaining high standards in patient care and ensuring the competence of medical professionals. From medical procedures to patient interaction techniques, ongoing training is essential to maintain competence and stay abreast of advancements in the field.

Training 52

Training Healthcare Healthcare Education 52

Legacy MEDSearch

APRIL 11, 2023

This system fills that void for both surgeons and patients.” Knee replacement is undoubtedly the gold standard for well-selected patients with severe OA, but for every patient I see that is ready for joint replacement, I see as many, if not more, who are not yet good arthroplasty candidates,” said William A.

Marketing 96

Marketing FDA Food and Drug Administration Specialization 96

Pharma Marketing Network

AUGUST 9, 2023

Adhere to Labeling and Packaging Requirements The labeling and packaging of pharmaceutical products are tightly regulated to ensure safety and accurate information. Train Your Team Educate your marketing and sales teams about the regulatory landscape and the importance of compliance.

Marketing 40

Marketing Pharma Food and Drug Administration Media 40

Legacy MEDSearch

AUGUST 29, 2022

Food and Drug Administration (FDA) has approved an investigational device exemption (IDE) application to initiate a pilot trial of the eShunt ® System in patients who develop communicating hydrocephalus post aneurysmal subarachnoid hemorrhage (paSAH). . Details on the trial will soon be posted to www.clinicaltrials.gov. About CereVasc, Inc.

FDA 52

FDA Food and Drug Administration Recruitment Physicians 52

Legacy MEDSearch

JULY 10, 2023

“This submission is another milestone in KORU Medical’s mission to make subcutaneous therapy radically simpler and easier for patients. . “This submission is another milestone in KORU Medical’s mission to make subcutaneous therapy radically simpler and easier for patients.

Medical 40

Medical Food and Drug Administration Recruitment Manufacturing 40

European Pharmaceutical Review

AUGUST 23, 2022

FAKE MEDICINES are not a new problem, and pose a tremendous threat to patient safety and public health in society regardless of a country’s economic status. Unfortunately, such a chain of custody is not intended to provide patients with the ability to verify their own medicines. This allows for a cyber?

Medicine 90

Medicine Food and Drug Administration Pharmaceutical products Pharmaceutical 90

Legacy MEDSearch

JUNE 16, 2023

The prospective, randomized clinical trial is designed to evaluate the safety and effectiveness of the pro disc C Vivo and pro disc C SK system by comparing it with an approved TDR product as a control for 2-level indications, making it the first and only of its kind with two investigational devices and a TDR control.

Food and Drug Administration 52

Food and Drug Administration Recruitment Safety Medical 52

Legacy MEDSearch

AUGUST 25, 2022

The PiCSO-AMI-II multicenter, randomized trial will enroll 300 patients with anterior ST-segment Elevation Myocardial Infarction (STEMI) presenting with TIMI flow 0, 1, and 2 within 12 hours of symptom onset. The primary safety endpoint is a performance goal for device and procedure related adverse events at 30 days.

Medical 52

Medical FDA Recruitment Pharmacology 52

Legacy MEDSearch

AUGUST 23, 2023

Food and Drug Administration (FDA) Circulatory Systems Devices Panel of the Medical Devices Advisory Committee met to discuss the pre-market approval application (PMA) for the Paradise Ultrasound Renal Denervation (RDN) system, indicated to reduce blood pressure in patients with hypertension. Otsuka Medical Devices Co.,

Medical 52

Medical Food and Drug Administration FDA Recruitment 52

Legacy MEDSearch

FEBRUARY 14, 2023

“Transcatheter mitral valve replacement is still in its infancy and is becoming an important therapeutic alternative for our patients with severe mitral regurgitation,” said Azeem Latib MD, Director of Interventional Cardiology, Montefiore Medical Center. million people, approximately four times more common than aortic stenosis.

Recruitment 52

Recruitment Management Medical Specialization 52

PM360

NOVEMBER 12, 2023

New entrants come into a therapeutic class, often with increased efficacy or safety, while older products lose patent exclusivity, changing the promotional landscape. Plus, the ways healthcare providers (HCPs) interact with both patients and pharmaceutical companies have seen significant changes.

Physicians 52

Physicians Media Electronics Pharmaceutical 52