Pharmaceutical Technology

JUNE 21, 2023

Ketarx will be marketed under the FDA-approved label of ketamine and in dosages that include 10mg/ml, 50mg/ml and 100mg/ml, with the option to boost the concentration and ready-to-administer applications. Ketamine is currently on the FDA’s drug shortage list. Ketarx will then be commercially launched in the second quarter.

Distribution 52

Distribution FDA Specialization Sales 52

Legacy MEDSearch

MAY 10, 2023

Food and Drug Administration (FDA) for continuous neonatal and infant monitoring for babies born of any gestational age to infants of 2 years at the International Maternal Newborn Health Conference in Cape Town, South Africa. The vast majority of medical devices used in pediatrics are not FDA-cleared or designed for children.

FDA 52

FDA Food and Drug Administration Recruitment Medical 52

Legacy MEDSearch

MARCH 16, 2023

Nurses or technicians can easily perform a bedside measurement and obtain a clear negative or positive output in less than 5 minutes without requiring specialized personnel or complicated equipment. For more information, visit [link]. Our clients include both blue-chip companies and innovative startups within the MedTech space.

FDA 52

FDA Patients Food and Drug Administration Recruitment 52

pharmaphorum

JANUARY 5, 2023

Addiction treatment specialist Spero Health has expanded an agreement to use Pear Therapeutics’ prescription digital therapeutics (DTx) in its network of US clinics. The extended agreement comes shortly after Pear reported a 24% quarter-over-quarter increase in revenues to $4.1

Prescription 52

Prescription Specialization FDA Networking 52

PM360

FEBRUARY 12, 2024

Given that less than 10% of rare diseases currently have an available treatment approved by the United States Food and Drug Administration (FDA) , advocating for the speedy development of novel drugs and therapies is a crucial step in improving the quality of life for those affected. What is a Rare Disease?

Food and Drug Administration 105

Food and Drug Administration Patients Networking Medical 105

Legacy MEDSearch

APRIL 3, 2023

ExtriCARE USA, is pleased to announce that its innovative extriCARE 3000 pump has received FDA approval for use in the United States. “We are thrilled to receive FDA approval for the extriCARE 3000 pump,” said Peter Mason , President of extriCARE USA.

Marketing 52

Marketing Recruitment Medical Distribution 52

MedTechVets

JULY 20, 2023

“ “Sometimes you may find that once you separate from the military that you miss the network, the camaraderie, the routine, and you may even find that you you’ve lost your sense of identity or purpose. It is also important to be willing and able to open and share your network.” Firstly, you must be humble.

Networking 52

Networking Medical Insurance Specialization 52

Legacy MEDSearch

FEBRUARY 2, 2023

Tyber Medical LLC has acquired 100 percent of the capital of ADSM-Synchro Medical, a French orthopedic medical device company, specializing in the development and distribution of implants dedicated to treating surgical forefoot pathologies. Bivi was formerly Vice President, Sales of Smith & Nephew Europe.

Medical 98

Medical Recruitment Marketing Distribution 98

Rep-Lite

MARCH 14, 2024

Specialized Certifications Specialized certifications can demonstrate a medical sales representative’s expertise and commitment to the industry. This also requires medical sales representatives to be familiar with clinical data based on research and FDA regulations to ensure compliance.

Medical sales reps 52

Medical sales reps Medical sales Medical Sales 52

Legacy MEDSearch

OCTOBER 27, 2023

an innovator in the field of orthopedic surgical robots, today announced that its TMINI Miniature Robotic System has received Special 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use with implants from three additional implant manufacturers. THINK Surgical, Inc., Are you hiring?

Specialization 52

Specialization FDA Food and Drug Administration Recruitment 52

Legacy MEDSearch

OCTOBER 25, 2023

Dr. Andrea Synowiec, a neurologist and headache specialist who serves as System Vice Chair of the Department of Neurology at Allegheny Health Network in Pennsylvania is the lead author of the study. We designed Nerivio with exactly these requirements in mind.”

Side effects 52

Side effects Recruitment Networking Management 52

PM360

OCTOBER 24, 2022

Proving as accurate as the gold standard PCR test, it was the first-ever FDA authorized use of CRISPR technology and demonstrated the power of CRISPR, while serving as a launch pad for the company’s advancements toward future applications that meet the needs of an evolving diagnostic landscape.

Medical 40

Medical Distribution Specialization Engineering 40

Nixon Gwilt Law

SEPTEMBER 7, 2023

Pediatric healthcare innovation companies—especially those in AR/VR/XR, Digital Therapeutics (“DTx”), Remote Monitoring, Virtual Care Management, Telehealth, and Telebehavioral health—need a deep understanding of the laws and regulations that govern this special market. The Family Educational Rights and Privacy Act (“FERPA”), is a U.S.

Food and Drug Administration 52

Food and Drug Administration Education Insurance Healthcare 52

Pharma Marketing Network

MARCH 25, 2022

The FDA has studied the importance of caregivers to drug development and regulatory decision-making. Sunny White is an Editorial Advisory Board member for the Pharma Marketing Network with unique insights into how important caregivers are to the HCP/patient relationship and overall health outcomes. What Can Pharma Do? Sunny White.

Pharma 98

Pharma Education Transportation Training 98

Contrarian Sales Techniques

DECEMBER 5, 2023

Keeping abreast of the latest regulations, like FDA approvals and industry guidelines, ensures that you're not just a salesperson, but a trusted advisor to your clients. Then there's the leap into specialized roles. Networking plays a pivotal role in opening doors to new opportunities, insights, and mentorships.

Pharmaceutical Sales 52

Pharmaceutical Sales Training Sales Pharmaceutical 52

Pharmaceutical Technology

SEPTEMBER 2, 2022

In a recent report, GlobalData revealed that the US Food and Drug Administration (FDA) approved 122 new drug applications (NDAs) and biologic license applications (BLAs) in 2021. The rate of drug approvals could be on the rise. This figure represents a 2.4% increase over the 2016–2020 period average. De-risking drug launch.

Food and Drug Administration 52

Food and Drug Administration Pharma Medicine Distribution 52

Legacy MEDSearch

JULY 24, 2023

Our clinic specializes in caring for the hardest and most hopeless, depressed patients by providing the best treatments available. a primary investigator and the first to enroll in the OLO study at Acacia Mental Health, Sunnyvale, Calif. “It About Magnus Magnus Medical, Inc. ,

Medical 52

Medical Recruitment FDA Specialization 52

Legacy MEDSearch

JULY 19, 2022

But before the platform became widely available, patients could only be diagnosed after trained sonographers performed an ultrasound in a hospital or specialized setting – typically after the onset of symptoms. since it received FDA 510(k) clearance in 2020.

Recruitment 52

Recruitment Medical Leads Patients 52

pharmaphorum

OCTOBER 27, 2022

Last month, pharmaphorum had the chance to speak with Dr Isabelle Ray-Coquard, professor of medical oncology (specialism sarcomas and GISTs) at the Centre Léon Bérard (CLB), a hospital 100% dedicated to cancer care and research. Ovarian cancer is the eighth most common cancer in women worldwide.

Patients 73

Patients Leads Specialization Networking 73

Legacy MEDSearch

MARCH 3, 2023

CMRs are considered the gold-standard cardiac diagnostic i ; however today, specially-trained CMR technologists need to perform an exam, and in the U.S., This case study will also be on display and discussed at Vista.ai’s ACC booth (#FH22) in the Future Hub. there is only one such technologist for every 20 MRI machines ii. About Vista.ai

Recruitment 52

Recruitment Training Patients Specialization 52

Pharma Marketing Network

JULY 7, 2021

Pfizer’s size, solid manufacturing capability and experience running large scale vaccine trials combined with BioNTech’s strong science created a synergistic effect that resulted in the first COVID-19 vaccine approved by the FDA for emergency use in December 2020, just 336 days after the genetic blueprint of the virus was published.

Pharma 59

Pharma Healthcare Healthcare Patients 59

PM360

DECEMBER 20, 2023

Addimmune , which is exploring gene therapy technologies that treat and cure HIV, went the special purpose acquisition company (SPAC) route where a publicly traded company is created for the purpose of acquiring or merging with an existing company. How did you approach your need for funding?

Management 109

Management Marketing Healthcare Healthcare 109

Rep-Lite

NOVEMBER 30, 2023

B2B sales consulting for medical sales is a specialized service that helps healthcare organizations navigate the unique challenges of B2B transactions within the healthcare industry. Then familiarize yourself with healthcare industry regulations like HIPAA and FDA standards, aligning your sales strategy accordingly.

B2B Sales 52

B2B Sales Medical sales Consulting Sales 52

Pharmaceutical Technology

JUNE 5, 2023

The US Food and Drug Administration (FDA) granted final approval to the therapy in May 2023. LUMRYZ represents a new generation of oxybate treatment that the FDA deems clinically superior to twice-nightly oxybate treatments. LUMRYZ is an extended-release formulation of sodium oxybate, indicated to be taken once at bedtime.

Food and Drug Administration 98

Food and Drug Administration Pharmaceutical Specialization FDA 98

pharmaphorum

OCTOBER 26, 2022

Founded in 1935 by Chiesi’s grandfather of the same name, Chiesi Group focuses on respiratory conditions, special care, and on rare diseases, including lysosomal storage disorders and rare haematological and ophthalmological diseases. “An These groups have also used patient feedback to build digital tools to help facilitate engagement.

Patients 80

Patients Pharma Consulting Transportation 80

PM360

SEPTEMBER 15, 2022

Cure” put me on a path to work across a network of incredibly smart, passionate, and well-meaning stakeholders to connect dots, create forums for sharing ideas, drive patient-centered approaches, and eliminate lost-in-translation moments. Fortunately, the industry is increasing its discussions around improving patient inclusion and DEI.

Patients 98

Patients Healthcare Healthcare Marketing 98

Legacy MEDSearch

JUNE 7, 2022

Food and Drug Administration (FDA) clearance for the company’s FreedomFlow® Peripheral Guidewire. Co-founded by Dr. Jihad Mustapha and Dr. Fadi Saab, ACV Centers has a special concentration on treating peripheral artery disease and the complications of critical limb ischemia. Cardio Flow, Inc., Are you hiring?

FDA 98

FDA Food and Drug Administration Recruitment Medical 98

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.

FDA 52

FDA Recruitment Marketing Medical 52

Legacy MEDSearch

MARCH 1, 2023

a medical imaging company focused on improving the treatment and outcomes for patients with coronary artery disease (CAD), today announced Food and Drug Administration (FDA) 510(k) clearance of their flagship intravascular imaging system, HyperVue. SpectraWAVE, Inc.,

Food and Drug Administration 97

Food and Drug Administration Physicians Recruitment Medical 97

Pharmaceutical Technology

MAY 24, 2023

Every major pharma company is now involved in CGT development which has resulted in the approval of 28 therapies by the FDA thereby making CGT no longer a niche category of therapies. CGT have highly unique and specialized manufacturing processes. This is a primary factor for the staggeringly high unit cost of CGT.

Manufacturing 98

Manufacturing Transportation Specialization Patients 98

Medgadget

JULY 18, 2022

Eric Brouwer: COVID-19 has had some impact on the availability of donor organs, specifically restricted access to surgery, new screening procedures being implemented, and exacerbation of shortages in specialized medical staff. Credit: University Health Network. FDA application.

Networking 76

Networking Medicine Transportation Leads 76

Evolve Your Success

DECEMBER 6, 2022

I am overjoyed to bring you a very special guest that goes by the name of Shirley Taylor. Now you’re talking about FDA-compliant equipment in the hospital space. ” so you can network together with each other and learn about opportunities. Tune in and learn what it takes to be one and thrive as one! What do you do?”

Sales 52

Sales Medical sales Medical Management 52

Pharma Marketing Network

JUNE 11, 2020

Yeah, I even wanted to wear the shirt to this FDA meeting. You know, in November 2009, the FDA held a public hearing about the promotion of Food and Drug Administrative Related Regulated Medical Products, using the internet and social media tools. Don Langsdorf (EHS): You’d mentioned 14 letters that the FDA sent.

Media 52

Media Pharma Ethics Consulting 52

Evolve Your Success

OCTOBER 31, 2023

— Watch the episode here Listen to the podcast here What A Field Clinical Engineer In Neuromodulation Sales Does With Blake Williams We have with us another special guest and he goes by the name of Blake Williams. FDA is happy with all of our results and our DMs are expressing that the physicians are happy with how everything is going.

Engineering 52

Engineering Sales Medical sales Physicians 52

Cadensee

JULY 5, 2021

Many companies especially in Europe go to local specialized distributors in different countries. Galit Zuckerman: I think we started with CE and FDA discussions the same time. We got a CE mark and the FDA, we're still in the process. I think you should use it; use these networks. use this network.

Physicians 52

Physicians Medical Patients Management 52

Legacy MEDSearch

OCTOBER 6, 2022

Body Vision Medical’s LungVision system was FDA cleared in 2019 and received CE Mark in 2021. Body Vision Medical specializes in AI-driven, intraoperative imaging with the aim of saving lives through the democratization of innovative medical technology. To learn more about Body Vision Medical, visit bodyvisionmedical.com.

Consulting 52

Consulting Medical Recruitment Marketing 52

Medgadget

JUNE 8, 2022

In the latest advancements of AI and med tech, the Eko DUO stands out as a smart and reliable product with FDA-cleared artificial intelligence (AI) algorithms being used to detect leading indicators of heart disease. The DUO can be used without the earpiece attachment altogether when paired with a mobile device.

Electronics 74

Electronics Leads Engineering Medical 74