Mon.Dec 26, 2022

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By Eliminating Requirement for Animal Testing, FDA Modernization Act Allows Faster, More Cost-effective Drug Development

MedCity News

By easing regulatory requirements for animal testing, the Act allows scientists to use innovative, leading-edge technologies more fully in future drug development strategies. .

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Top Stories of 2022 for Books and Reading

Copyright Clearance Center

The post Top Stories of 2022 for Books and Reading appeared first on Copyright Clearance Center.

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Healthcare Access and Equity: Women’s Health and Technology Hold the Keys

MedCity News

If women are the influential guide for many to access healthcare, we must work harder to promote the health of all women. Our ability to play the role of care facilitator for others depends upon it.

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11 Ways To Succeed At Telecom Sales

Spotio

The global telecommunications market is poised for huge growth. In fact, it’s forecasted to grow to $13.76 billion by 2031. How big is your slice of that pie? Ultimately, that will depend on how successful you are as a sales rep. In telecom sales, the most valuable reps are the ones that get out the door and talk face-to-face with their customers. They can use the hard work they’ve put into researching and understanding their product to answer questions in person and help customers find the best

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Unlocking Excellence: How Catalent Is Transforming Japan’s Clinical Research

Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud

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It’s Almost 2023 – Why Are Patient Experiences Still So Terrible?

MedCity News

The FHIR APIs mandated by CMS are only one data format, designed for the fast exchange of electronic health records.There’s a larger category of APIs that will help us provide a simpler, more integrated process: experience APIs.

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What I Learned In Three Years As An Entry Level Sales Rep?

Medical Sales Authority

Entry level sales job are hard. They serve to weed out a good chuck of the people interested in sales. The pay is not great, the products are boring, and the hours are long. There is typically less autonomy and more scrutiny from management about productivity. The key is putting in the time and grinding through this period. This will lead to higher pay, more interesting products, and more flexibility down the line.

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LegoChem, Amgen partner to develop antibody drug conjugates

Pharmaceutical Technology

LegoChem Biosciences and Amgen have signed a multi-target research collaboration and license agreement to develop antibody-drug conjugates (ADC). Under the deal terms, Amgen was granted rights for the research, development, and commercialisation of ADCs that will be directed to treat up to five targets which are chosen by the company using the ConjuAll ADC technology of LegoChem.

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How Healthcare Practices Can Achieve True Interoperability—And What That Means for the Business

MedCity News

As we shift into a modern era of healthcare, it’s becoming clear that no tool can be a one-size-fits-all solution, including most EHR systems. Supporting technology, then, needs to be implemented to ensure systems can effectively talk to one another to improve the quality of services and the performance of practices.

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Top 5 Articles for Retail Pharmacists in 2022

Pharmacy Times

This year, retail pharmacists were interested in diabetes research, saving patients money, and influenza vaccine candidates.

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Taboos With Telehealth: Is the Vimpro Model the Future of Men’s Healthcare?

MedCity News

If men’s health outcomes are to be improved, we need to create new pathways for men to access healthcare – pathways that swerve these social barriers.

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How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.

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Transparency Makes Cost-Plus Drug Pharmacies a Unique Business Model

Pharmacy Times

Without company or insurance contracts, controlled medication prices reduce burden on patients.

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Business ecosystems in asset finance: Greater than the sum of their parts

Pharmaceutical Technology

The once cut-throat business landscape is evolving, and business ecosystems are on the rise. Open APIs are facilitating unprecedented collaboration, enabling businesses to pool their resources and expertise to develop better solutions for end users. The opportunities for new innovations and functionalities are enormous. “Companies have long looked at collaboration to increase value, but the idea of expanding such partnerships on a technical basis was enabled by the rise of the internet and linke