Sat.Dec 05, 2020 - Fri.Dec 11, 2020

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Novartis signs ophthalmology AI deal with RetinAI Medical

pharmaphorum

Novartis has signed a multi-year agreement with RetinAI Medical, which will see the companies work together to use artificial intelligence (AI) tools to support ophthalmology and digital health projects. Both companies have already worked on pilot projects in this area. The first project under a new master agreement will involve a multi-centre international clinical study involving patients with neovascular age-related macular degeneration (nAMD).

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RWE key to boosting trial diversity: Verantos

Outsourcing Pharma

An expert from the clinical research technology specialist discusses how trial teams can use real-world evidence to improve study inclusivity.

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17 creams to STOP ITCHING FAST

Druggist

Several factors can cause skin itchiness (also known as pruritus). Skin itch is commonly associated with eczema (dermatitis), psoriasis, chickenpox, insect bites, hives and other conditions. Several effective creams to stop itching can be purchased from supermarkets, pharmacies and online. Sale of some anti-itch creams is restricted to pharmacies only.

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Gilead’s CAR T therapy Yescarta shows potential in new indication

Pharma Times

ZUMA-12 phase II study is evaluating therapy as a first-line treatment for high-risk large B-cell lymphoma

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From Diagnosis to Delivery: How AI is Revolutionizing the Patient Experience

Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.

The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven

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Cyberattack targets EMA, hacks COVID-19 vaccine data

pharmaphorum

The European Medicines Agency (EMA) says it suffered a cyberattack, with documents relating to a Pfizer and BioNTech’s COVID-19 vaccine accessed. In a terse statement, the EU regulator confirmed its security had been breached and said it had launched an investigation with law enforcement, but would not be providing any additional information while that probe was underway.

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CROs partner on women’s oncology clinical solutions

Outsourcing Pharma

Health Decisions and OncoBay Clinical will collaborate on specialized clinical development services addressing therapies for womenâs cancers.

More Trending

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Roche reveals new bispecific antibody data in blood cancers

Pharma Times

'Encouraging' data for investigational candidates across a range of blood cancers

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FDA reviewers back Pfizer/BioNTech COVID-19 vaccine ahead of panel

pharmaphorum

Reviewers from the FDA have given their blessing to the Pfizer/BioNTech COVID-19 vaccine ahead of a key meeting tomorrow – but the regulator noted that there are still uncertainties about whether the shot can stop the disease from spreading. The gist of a briefing document published from FDA reviewers ahead of an expert advisory board meeting is that the vaccine is good to go.

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Medidata: collaboration furthers decentralized trial progress

Outsourcing Pharma

Through organizations like the Association of Clinical Research Organizations, clinical research professionals are helping decentralized research evolve.

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What a Clinical Trial Transparency Program Is (and Why You Need One)

Pharma Marketing Network

Tune in now to listen to Darshan Talks Podcast, What a Clinical Trial Transparency Program Is (and Why You Need One). The post What a Clinical Trial Transparency Program Is (and Why You Need One) appeared first on Pharma Marketing Network.

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Position Your Pharmacy for Expansion

Speaker: Chris Antypas and Josh Halladay

Access to limited distribution drugs and payer contracts are key to pharmacy expansion. But how do you prepare your operations to take the next step? Meaningful data: Collect and share clinical data regarding outcomes, utilization, and more Reporting: Limited distribution models require efficient tracking and reporting systems Workflows: Align workflows with specific pharma and payer contractual requirements For in-depth, expert insights on pharmacy expansion, watch this webinar from Inovalon.

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MHRA issues allergy warning for Pfizer/BioNTech COVID-19 jab

Pharma Times

Updated guidance warns people with a history of allergic reactions not to receive the shot

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AI drug discovery biotech AbCellera eyes record IPO

pharmaphorum

AbCellera Biologics has been in the spotlight since coming up with Eli Lilly’s COVID-19 antibody drug bamlanivimab, and looks set to capitalise on that exposure with a sizeable initial public offering. The Vancouver, Canada-headquartered biotech – which has been bankrolled in part by billionaire entrepreneur and venture capitalist Peter Thiel – plans to offer 23 million shares at a price of between $14 and 17%, which could raise $380 to $390 million.

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FDA grants orphan status to Rafael Pharmaceuticals cancer drug

Outsourcing Pharma

The companyâs cancer drug, devimistat, has received orphan status from the agency for treating clear-cell sarcoma, pancreatic cancer, and other diseases.

FDA
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Telstar strengthens its activity in Bangladesh and relocates its office in Dhaka

Pharma Mirror

Terrassa (Barcelona) 2020. The Telstar subsidiary in Dhaka, Bangladesh, has relocated to a new installation reacting to the ongoing growth of demand for Life Sciences service & product solutions in the region. Under the leadership of Parvez Hashim, Country General Manager, Telstar’s office has consolidated a professional and specialized service in Asia’s pharmaceutical market in consultancy, engineering, construction and manufacturing processes for development of turnkey plants and installat

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What the FDA's New Dosage Guidance Means for the Future of Clinical Research

Speaker: Dr. Ben Locwin - Biopharmaceutical Executive & Healthcare Futurist

What will the future hold for clinical research? A recent draft from the FDA provides valuable insight. In "Optimizing the Dosage of Human Prescription Drugs and Biological Products for the Treatment of Oncologic Diseases," the FDA notes that "targeted therapies demonstrate different dose-response relationships compared to cytotoxic chemotherapy, such that doses below the Maximum Tolerated Dose (MTD) may have similar efficacy to the MTD but with fewer toxicities.

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Winners shine bright at PharmaTimes Awards

Pharma Times

Meet the winners of the 2020 PharmaTimes Marketer of the Year, Communications Awards and Sales Awards

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Sanofi/Regeneron on notice as FDA reviews GSK’s Nucala for nasal polyps

pharmaphorum

Sanofi and Regeneron’s Dupixent has had the US market for the treatment of chronic rhinosinusitis with nasal polyps (CRSwNP) mainly to itself since June 2019, but GlaxoSmithKline’s Nucala is now breathing down its neck. The FDA has started its review of Nucala (mepolizumab) for the inflammatory condition, which results in the growth of nasal polyps in the nose that can obstruct airflow and cause mucus discharge, sometimes requiring surgical intervention.

FDA
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How has COVID-19 impacted clinical trial data collection?

Outsourcing Pharma

A leader from data-centric CRO Quanticate shares perspective on how the pandemic has disrupted trials, and what tools and technologies can keep work going.

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Frugal Living? 2 Smart Money Moves to Make Before Year End

That Frugal Pharmacist

I’m That Frugal Pharmacist, so clearly I should have some ideas about frugal living, right? 2020 has been a heck of a year for everyone. I’ve got two big tips to either make the most of your frugal muscle, or make some smart money moves and start maximizing your money. Clearly, you should be tracking … Frugal Living?

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5 Reasons to Upgrade Your Pharmacy Management Software

Are you still using workarounds to manage your daily operations? To achieve peak performance, it's time to explore other options for specialty and infusion pharmacy software. Streamline pharmacy operations and improve clinical performance with automated processing, real-time data exchange, and electronic decision support. Download this helpful infographic to: Drive efficiency and patient adherence from referral receipt to delivery and ongoing care – all with our Pharmacy Cloud.

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Research highlights benefit of telemedicine for stroke treatment

Pharma Times

Around one in five stroke patients could go undiagnosed with the tests currently used by paramedics

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Latin America: How pharma can navigate a complex market

pharmaphorum

Bureaucracy, political upheaval, and lack of regulations continue to make Latin America a difficult market for European and North American pharma to enter – and COVID-19 has only worsened these issues. Developing market specialist Dr Zulf Masters OBE takes us through the nuances of being successful in this region. Having worked all around the world to supply medicines to developing markets, Dr Zulf Masters understands the biggest barrier for a pharma company entering these regions is a lack of u

FDA
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Ancestry study explores COVID-19 genetic risks

Outsourcing Pharma

The online DNA network has delved into self-reported data of more than 563,000 US adults to help identify genetic risk of infection and severe outcomes.

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CO2 Safety Monitors for Dry Ice Vaccination

Pharma Mirror

Ormond Beach, FL – CO2Meter, Inc. has partnered with a national pharmacy chain to keep their customers and employees safe from the potential hazardous effects for CO2 exposure from the dry ice that is keeping the COVID-19 vaccines cold. A national pharmacy chain contacted CO2Meter on December 1st asking about devices to detect the release of CO2 when dry ice sublimates.

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World first as UK launches COVID-19 vaccination programme

Pharma Times

A 90 year-old woman in Coventry has become the first person in the UK to be given the vaccine

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Coronavirus vaccine may have allergy warning in US, says expert

pharmaphorum

The US government’s coronavirus vaccine chief has said that Pfizer/BioNTech’s vaccine could carry a warning that it should be avoided by people who are prone to serious allergic reactions. Moncef Slaoui, co-head of the US government’s Operation Warp Speed COVID-19 vaccine programme, made the comments after the UK drugs regulator advised those with severe allergies to avoid the vaccine.

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Current FDA COVID-19 developments

Outsourcing Pharma

The agency continues to offer advice, resources and oversight during the pandemic to help develop tests, treatments and other solutions for the virus.

FDA
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Biotech Showcase | January 11-15, 2021 | Digital Event

Pharma Marketing Network

REGISTER NOW! The post Biotech Showcase | January 11-15, 2021 | Digital Event appeared first on Pharma Marketing Network.

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NICE backs AZ' Calquence for chronic lymphocytic leukaemia

Pharma Times

The recommendations are positive for a select population of patients with CLL

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UK faces “V-Day” and largest ever vaccination programme

pharmaphorum

Tuesday has been dubbed “V-day” in the UK, when the first doses of Pfizer/BioNTech’s coronavirus vaccine will be distributed to the public outside of a clinical trial. Health secretary Matt Hancock reportedly came up with the wartime analogy to describe what will be the largest scale vaccination programme in the country’s history. The UK last week became the first country in the world to officially authorise the vaccine, which has so far shown an effectiveness of around 95% and minimal side effe

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What Should an Ambulatory Surgery Center Look for in a Pharmacy Partner?

indispensable health

What are good Characteristics of a pharmacy partner for an Ambulatory Surgery Center? When considering what characteristics an Ambulatory Surgery Center (ASC) should consider in a pharmacy partner “flexibility” is the first that comes to mind. Ambulatory Surgery Centers require a pharmacy partner that can be flexible to their unique situations. Every ASC has various needs and pharmacy providers must be able to provide custom services tailored to fit the outpatient surgery center’s needs.

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CPhI report looks ahead to post-COVID pharma world

Outsourcing Pharma

The industry analysis dives into likely developments in supply chain, impact of the new White House occupant, CDMO growth and other key areas.

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FDA set to review GSK’s Nucala for nasal polyps

Pharma Times

Submission is based on data from the pivotal SYNAPSE study

FDA
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Sensyne launches fundraising, agrees patient data deal with Phesi

pharmaphorum

UK digital health firm Sensyne has secured access to millions more anonymised patent records via an alliance with US clinical trial data specialist Phesi. The new agreement comes after a string of access deals with NHS trusts for patient data, and coincides with a bid by Sensyne to raise £27.5 million (around $37 million) through a 90 pence per share placing.

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Is Off-Label Marketing by a Pharma Company a Bad Thing?

Pharma Marketing Network

Tune in now to listen to Darshan Talks Podcast, Is Off-Label Marketing by a Pharma Company a Bad Thing? The post Is Off-Label Marketing by a Pharma Company a Bad Thing? appeared first on Pharma Marketing Network.