pharmaphorum

JUNE 15, 2022

The drug works by activating the body’s natural response to reduced oxygen levels in the blood, increasing red blood cell production. ” It’s estimated that more than 75,000 people live with anaemia associated with CKD in England and Wales.

Nurses 57

Nurses Marketing Clinical Trials Clinical Trials 57

pharmaphorum

FEBRUARY 23, 2022

Ben Hargreaves takes a look at why uptake began slowly in both the EU and the US, and then began to accelerate to see biosimilars take a large portion of market share away from originator products. One way in which the pharmaceutical industry and regulators have reacted is by developing or facilitating the development of biosimilars.

Marketing 87

Marketing Production Development Medicine 87

pharmaphorum

MARCH 18, 2022

Allergan fell foul of the regulations for a number of LinkedIn and Instagram posts promoting Botox (botulinum toxin type A) to the public by the chief executive of aesthetics clinic – described in his profile as an ‘Allergan mentee’, which were also liked or commented on by employees of the company.

Botox 62

Botox Medicine Nurses Sales 62

XTalks

AUGUST 12, 2020

of Bakersfield, California, USA, or any products made with these onions. This advice applies to all individuals across Canada, as well as retailers, distributors, manufacturers and food service establishments such as hotels, restaurants, cafeterias, hospitals and nursing homes.”. More about Salmonella.

Contamination 78

Contamination Production Bacteria Nurses 78

pharmaphorum

NOVEMBER 1, 2021

How can pharma move from a product- to a patient-centric mindset? We need to engage with them if we are to develop new products and solutions that create better health for everyone,” she said. As well as digital tools and nurse visits, they sometimes wanted to see the doctor,” she said. We were very proud of it.

Clinical Trials 64

Clinical Trials Clinical Trials Trials Production 64

pharmaphorum

JANUARY 12, 2023

As the crisis rumbles on, there is a risk of greater levels of drug diversion, which requires a counter strategy on the part of the healthcare care industry and regulators.

Drugs 90

Drugs Nurses Medicine Regulation 90

XTalks

AUGUST 2, 2022

Baxter has recommended that Abacus users follow instructions outlined in the user and configuration guides for the product prior to processing orders. They also suggest having a pharmacist review orders and that both pharmacy and nurse checks be conducted on every order.

Drugs 52

Drugs Nurses Pharmacy Production 52

XTalks

FEBRUARY 10, 2023

As a result of this siloed decision-making and planning, confirmation of suitability of the protocol and product design may occur much later during regulatory submission or patient enrollment, thereby requiring re-work, timeline delays and an increased budget. Medpace Regulatory Team support throughout product development.

Clinical Trials 52

Clinical Trials Clinical Trials Trials Gene Therapy 52

XTalks

AUGUST 25, 2021

But now that restrictions are loosening, more and more retail settings are offering food samples once again — an encouraging sign for smaller brands that rely on it to get its products into the hands of consumers. . Much like all things pre-pandemic, food sampling took a hit throughout most of 2020 and into 2021.

Branding 98

Branding Marketing Nurses Production 98

pharmaphorum

AUGUST 23, 2021

The regulator has cleared the vaccine – now officially given the trade name Comirnaty – to prevent COVID-19 in people aged 16 or more, although it will still be available to 12 to 15 year olds under the EUA. . Having a fully-approved vaccine could also encourage businesses and other organisations to insist on vaccination.

Vaccination 52

Vaccination Vaccine FDA Approval Nurses 52

Pharmacy Checkers

NOVEMBER 21, 2019

As my greater advocacy initiatives have worked to implore the FDA to bring more balance, commonsense and fairness to regulating and providing consumer education about personal imports of prescription drugs, I’ve realized that I should practice the same in how I talk about the FDA. The medications that we obtain in the U.S., Far from it.

Generic Drugs 68

Generic Drugs Manufacturing Regulation Drugs 68

The Pharma Data

AUGUST 28, 2020

The Department of Health and Social Care (DHSC) said this could include training a wider range of existing NHS staff, as well as student doctors and nurses. Proposals, which are being considered in a three-week consultation , are designed to cut red tape and prevent any delays between a vaccine being found and then given to the UK population.

Vaccination 52

Vaccination Vaccine Immune Response Nurses 52

The Pharma Data

NOVEMBER 30, 2020

. “If people with heart failure can reduce the amount of pro-inflammatory foods that they eat, it might help with their survival,” said lead researcher JungHee Kang, a nursing research assistant and PhD student at the University of Kentucky in Lexington.

Cardiology 52

Cardiology Nurses Research Production 52

Roots Analysis

FEBRUARY 21, 2024

In addition, several exoskeletons can help healthcare workers, such as doctors and nurses in physically demanding tasks and repetitive work to avoid back injuries. In smart factories, the Industrial Internet of Things (IIoT) facilitates seamless integration of exoskeletons to enhance worker safety and productivity.

Marketing 40

Marketing Regulation Production Nurses 40

Pfizer

JANUARY 27, 2023

The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. AUTHORIZED USE The U.S.

Marketing 75

Marketing Production Drugs Licensing 75

Pharmacy Checkers

JANUARY 10, 2020

We know there are many doctors, nurses and other prescribing medical professionals who recommend PharmacyChecker or have learned of trusted licensed foreign pharmacies though their own research. FDA and Alipza by the United Kingdom Medical and Health Product Regulatory Authority. FDA: PIERRE FABRE MEDICAMENT PRODUCTION.

FDA Approval 62

FDA Approval Branding Pharmacy Manufacturing 62

Pharma Marketing Network

SEPTEMBER 14, 2020

Give your staff, reps, and other KOLs the chance to create personalized videos to thank local HCPs, nurses, and others on the front line of the coronavirus crisis. For the heavily-regulated healthcare industry, these platforms help maintain compliance with built-in processes and tools to ensure proper permissions are granted at each stage.

Sales 105

Sales Pharma Companies Nurses Compliance 105

Pfizer

JANUARY 27, 2023

and global regulators for all antiviral products and are carried out by many companies and academic institutions in the U.S. It is important to note that these studies are required by U.S. and around the world. IMPORTANT SAFETY INFORMATION Pfizer-BioNTech COVID-19 Vaccine, Bivalent (Original and Omicron BA.4/BA.5),

Research 112

Research Vaccination Vaccine Drugs 112

Pfizer

AUGUST 15, 2022

The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. Herbal Products: St. AUTHORIZED USE. anti-infectives).

Drugs 99

Drugs Vaccination Vaccine In-Vitro 99

Cloudbyz

MARCH 12, 2023

Review documentation Review the site’s regulatory and institutional review board (IRB) documentation to ensure that it is up to date and in compliance with local regulations. This includes reviewing the storage, security, and access control measures in place for investigational products and study documents.

Nurses 52

Nurses Compliance Clinical Trials Clinical Trials 52

Pfizer

DECEMBER 13, 2022

The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. Herbal Products: St. AUTHORIZED USE . Antimycobacterials: rifampin.

Drugs 110

Drugs Licensing Licensing Production 110

Advarra

APRIL 30, 2024

Verify names, address(es), and other relevant information are correct for the following: All investigator sites where the participants are seen for trial procedures and the investigational product (IP) shipment address(es) are recorded in section 3. In some countries, local regulations may indicate the sub-investigators need to sign as well.

Licensing 52

Licensing Licensing Pharmacy Clinical Trials 52

Pharma Marketing Network

SEPTEMBER 14, 2020

Give your staff, reps, and other KOLs the chance to create personalized videos to thank local HCPs, nurses, and others on the front line of the coronavirus crisis. For the heavily-regulated healthcare industry, these platforms help maintain compliance with built-in processes and tools to ensure proper permissions are granted at each stage.

Sales 69

Sales Pharma Companies Nurses Compliance 69

The Pharma Data

OCTOBER 18, 2020

Richner received a Master of Public Health in Health Policy and Administration and a Bachelor of Science in Nursing from the University of Michigan in Ann Arbor, Michigan. Throughout my career, I have sought to enable access to breakthrough technologies as an important element of public health policy.

Production 52

Production Marketing Containment Sales 52

Pfizer

DECEMBER 20, 2022

The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. Herbal Products: St. AUTHORIZED USE. Anticancer drugs: apalutamide.

Drugs 69

Drugs Licensing Licensing Containment 69

XTalks

JANUARY 19, 2022

The webinar also included three case studies which used remote biosensor technology in DCTs, which were described by Mariel Fabro, Head of Products at Vivalink, a company which provides digital healthcare solutions for virtual patient care and DCTs. The future of DCTs and HCTs certainly looks promising in a post-pandemic world.

Clinical Trials 98

Clinical Trials Clinical Trials Trials Clinical Research 98

XTalks

MAY 10, 2024

For the 2024-2025 flu season, the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) has recommended a trivalent influenza vaccine formulation, which excludes the B/Yamagata strain. For manufacturers, three versus four strains in the vaccine perhaps simplifies manufacturing.

Vaccination 52

Vaccination Vaccine Life Science Nurses 52

pharmaphorum

MAY 20, 2022

CVS Health has come a long way from its humble beginnings as a health and beauty products store in 1963. And so that’s kind of I think lesson number one is just that clinical research is a complex, regulated, established market with its own adoption curve. The patient wants to be able to interact with studies on their own terms.

Clinical Trials 89

Clinical Trials Clinical Trials Trials Clinical Research 89

The Pharma Data

OCTOBER 25, 2020

The Richmond Agitation–Sedation Scale was developed in a collaborative effort with practitioners representing critical care physicians, nurses, and pharmacists and its validation and reliability is well documented. Food and Drug Administration (“FDA”) for the treatment of agitation associated with delirium. BioXcel Therapeutics, Inc.

Trials 52

Trials Production FDA Approval Development 52

Delveinsight

FEBRUARY 17, 2021

To fulfill the patient’s evolving needs and to provide them with better services, companies worldwide are focusing on delivering new applications and products to the users. Besides it is in use to analyze population health trends, medical records, virtual nursing assistants, and administrative work.

Doctors 52

Doctors Doctor Big Data Development 52

pharmaphorum

APRIL 16, 2021

Approval by regulators such as the FDA or EMA, as reported by the regulators themselves. This wasn’t the case in Germany, where a resilient system meant that productivity in terms of HTA decisions was higher in 2020 than the historic average from 2015-2019. ” In the UK and France, HTA decision making slowed down.

Sales 74

Sales Marketing Medicine Doctors 74

ACRP blog

MAY 17, 2023

Sidebar 2: Informal Poll at ACRP 2023 Finds Regulations to be “Clear as Mud!” Nearly 50% said the regulations were “clear as mud” and nearly 50% wished “someone would send help” for dealing with the challenges faced. The draft guidance offers welcome clarity that this is still the case for DCTs.

Clinical Trials 59

Clinical Trials Clinical Trials Trials Clinical Research 59

Drug Discovery World

OCTOBER 19, 2022

She explains how the centre responded to the initial invasion: “Our centre did not stop its work for more than a day, and all principal investigators, coordinators and nurses stayed in Kyiv. We quickly made the decision to use the capacity of a large local laboratory with which we are collaborating to monitor patient safety.

Clinical Research 52

Clinical Research Research Clinical Trials Clinical Trials 52

The Pharma Data

FEBRUARY 8, 2021

This PTE will be listed in Approved Drug Products with Therapeutic Equivalence Evaluations (commonly known as the Orange Book), published by the U.S. IBRANCE is an oral inhibitor of CDKs 4 and 6, 1 which are key regulators of the cell cycle that trigger cellular progression. Food and Drug Administration (FDA). 2,3 In the U.S.,

HR 52

HR Clinical Trials Clinical Trials Containment 52

Pfizer

NOVEMBER 23, 2022

The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. Herbal Products: St. AUTHORIZED USE. Antimycobacterials: rifampin.

Licensing 40

Licensing Licensing Drugs Manufacturing 40

Pharma Marketing Network

NOVEMBER 4, 2020

Tom (AC): Yeah so we have a two products one is a self-service to what we were searching audience generate the ads from scratch. So people will buying this alcoholic products to say sorry like the brand have no idea about it so we have another thing which is like your only get data back on the things that you test.

Branding 52

Branding Marketing Regulation Production 52

The Pharma Data

APRIL 8, 2021

Roche’s Chief Medical Officer and Head of Global Product Development. “We Roche will present data on the increased use of home nursing capabilities in the Phase III GRADUATE studies of gantenerumab during the COVID-19 pandemic, which enabled home-bound trial participants to continue dosing to maintain medicine exposure.

Clinical Trials 52

Clinical Trials Clinical Trials Trials Antibody 52