European Pharmaceutical Review
JULY 4, 2024
Altering the conditions that T cells are grown in can improve CAR T-cell therapy, US researchers have found. Discovered by chance, their new method has potential to treat solid cancer tumours more efficiently, according to the findings. Putting T cells on a keto diet [putting our T cells on a three-day ‘keto’ diet] showed reduced maturity at the end of the manufacturing process.
pharmaphorum
JULY 4, 2024
Pieris' immuno-oncology alliance with Servier is being dissolved after a trial of the lead drug in the alliance revealed a safety concern.
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European Pharmaceutical Review
JULY 4, 2024
In the US, botanical dietary supplements can be sold without US Food and Drug Administration (FDA) approval, 1 prompting many vendors to promote the use of botanical products as dietary supplements , 2 rather than pursue a path of regulatory approval. However, as with drugs, dietary supplements require evidence that they are safe and that claims on product labels are truthful and not misleading. 1 For use as prescription drugs, a botanical product must be approved by the FDA: to date, only two h
pharmaphorum
JULY 4, 2024
UK survey finds more than two-thirds of people with chronic hand eczema say it has affected their relationships and/or working life.
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Quotas need to be hit. Revenue goals need to be met. This reality makes shortening sales onboarding time a top priority. Organizations with a standard onboarding process boost employee retention by 58% and increase productivity by 50%. Unfortunately, many companies struggle with inefficient processes that lead to high turnover and missed revenue opportunities.
PharmaTimes
JULY 4, 2024
Aggressive prostate cancer accounts for up to 15% of all prostate cancer diagnoses
pharmaphorum
JULY 4, 2024
A Connecticut federal judge has rejected Boehringer Ingelheim's challenge to Medicare’s drug price negotiation programme.
Pharma Rep Focus brings together the best content for pharma rep professionals from the widest variety of industry thought leaders.
Infuse Medical
JULY 4, 2024
In the new era of health care, interactive patient education is vital to make patients understand their health easier, more engaging, and highly personalized web. Imagine learning about your health through captivating videos. That’s the ideology behind interactive patient education content creation. The clearer the understanding of a disease, the more likely an individual is to follow necessary treatment procedures.
PharmExec
JULY 4, 2024
OncLive serves as the connection to oncology, including groundbreaking cancer news and interviews with top oncologists in multimedia formats.
Infuse Medical
JULY 4, 2024
The growing field of medical information and technology is always looking for the best possible care for their patients. With the constant influx of new data and tools, it can be overwhelming to stay updated and make informed decisions. Here comes AR technology as a trailblazer in the hospital sector. This is changing the way healthcare professionals interact with patients and access critical information.
PharmExec
JULY 4, 2024
OncLive serves as the connection to oncology, including groundbreaking cancer news and interviews with top oncologists in multimedia formats.
Infuse Medical
JULY 4, 2024
VR in healthcare is doing magic by transforming the conventional working environment to the next level. It simulates real-world scenarios in a controlled, virtual environment. VR training enables medical device maintenance personnel to practice and refine their skills without the risks associated with live equipment. This innovative approach improves technical proficiency and reduces the learning curve.
Pharmaceutical Commerce
JULY 4, 2024
The investment is expected to help enhance the company temperature-controlled services in the Netherlands, France Italy, and Hungary.
Infuse Medical
JULY 4, 2024
Are you considering importing medical device? Or else looking to manufacture medical equipment in the United States? If so, it is important to understand the regulatory requirements of the FDA. Do you know the FDA is the Food and Drug Administration? Yes!! It regulates all medical devices in the United States. It is essential to understand the FDA’s definition of a medical device.
PharmaTech
JULY 4, 2024
HCPs are major process-related impurities that must be monitored throughout biologics production for clearance.
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Are your sellers unsure about using AI in their day-to-day workflows? Or are they eager to try but uncertain where to start? They might be asking: Which tasks are best suited for AI? How will using AI affect my relationship with my customers? With so many tools available, which ones are the most useful to me? To help answer these and other common questions about using AI during the sales cycle, we surveyed B2B sellers who were early adopters to get their insight and advice about how to use gen A
Pharmaceutical Commerce
JULY 4, 2024
The latest news for pharma industry insiders.
PharmaTech
JULY 4, 2024
The companies have restructured their existing collaboration into a licensing agreement that invests in mRNA development.
Pharmacy Times
JULY 4, 2024
This narrative review dispels the long-held belief that reduction in salt intake leads to better health outcomes in patients with heart failure.
PharmaTech
JULY 4, 2024
LenioBio and Labscoop's new strategic partnership is aimed at increasing access to scalable cell-free protein synthesis technology across North America.
Pharmacy Times
JULY 4, 2024
Investigators found improvements over the placebo in metabolic dysfunction-associated steatohepatitis without worsening fibrosis across 3 dosing groups.
Pharmacy Times
JULY 4, 2024
Many patients who took technosphere insulin saw improvements in hemoglobin A1c, but other patients saw worsening with the drug.
Pharmacy Times
JULY 4, 2024
The UK’s Medicine and Healthcare Products Regulatory Agency (MHRA) introduced changes to streamline its drug approval processes.
Pharmacy Times
JULY 4, 2024
Antibody-drug conjugates (ADCs) revolutionize cancer therapy by delivering powerful drugs directly to tumors and minimize damage to healthy cells.
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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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