Definitive Healthcare

AUGUST 8, 2022

Resource Type Whitepapers & Research Marketo form number 1747 Case Study Buyer's Guide Whitepaper Transforming a sales team with data-driven market intelligence from Definitive … Healthcare data & analytics buying guide for medical device firms Shifting point of care to ambulatory surgery centers Image Image Image ","nextArrow":" ","appendArrows":".coh-slider-nav-bottom","dots":false,"draggable":true,"swipe":true,"fade":false,"vertical":false,"speed":700,"cssEase":"ease","pauseOnHo

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LifeProNow

MAY 4, 2023

FDA is taking additional steps to support the use of decentralized clinical trials (DCTs) for drugs, biologics and devices, where some or all the trial-related activities occur at locations other than traditional clinical trial sites.

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Packaging 130

pharmaphorum

JUNE 16, 2022

Jennifer discusses how Abbott has approached these issues in the clinical trials for their vascular medical devices. They discuss the nitty-gritty of clinical trial diversity – why it’s been so hard to achieve, why it’s important, and how to overcome the specific barriers to inclusion for different underrepresented communities.

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Pharmaceutical Technology

DECEMBER 27, 2022

Along the way, mergers and acquisitions continued to happen, new drugs and devices got approved, and innovations in the clinical trial industry were introduced. Drug pricing was a hot-button topic, and William Newton found that while e-commerce chains could cut insulin prices , any major change won’t happen overnight. See you in 2023!

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FDA Law Blog: Biosimilars

AUGUST 28, 2023

Lenz, Principal Medical Device Regulation Expert — Following up on our first post discussing Digital Health Technologies (DHTs) ( here ), this post will focus on development and qualification of DHTs for use in clinical trials for drug development. By Adrienne R.

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Drug Development 59

FDA Law Blog: Biosimilars

AUGUST 7, 2023

By Véronique Li, Senior Medical Device Regulation Expert — The Center for Devices and Radiological Health (CDRH) offers learning opportunities for new and experienced CDRH staff through the Experiential Learning Program (ELP).

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pharmaphorum

SEPTEMBER 21, 2020

Amazon’s Alexa device can already field health and medical questions, but the library of responses has now been bulked up thanks to a partnership with digital health company Sharecare. billion at the end of 2018, according to market research. billion at the end of 2018, according to market research.

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Mayo Clinic HIPAA Online Pharmacies 138

FDA Law Blog: Biosimilars

FEBRUARY 26, 2024

Walsh among an elite panel discussing “Around the World Hot Topics” – a session dedicated to exploring recent enforcement trends, regulator expectations, and best practices in white-collar crime law. With over 26 years of dedicated service to the pharmaceutical and medical device industries, Ms.

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Express Pharma

JULY 14, 2023

The platform imparted informative sessions on wide range of topics, including investigational skills for counterfeit drugs, legal drafting, blood center inspections, medical devices rules, good regulatory practices. Rakesh Dahiya along with Gen. Secretary, Baldev Chowdhary, were present.

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pharmaphorum

FEBRUARY 25, 2021

Drug Delivery Devices Symposium. We have the distinct privilege of unveiling Oxford Global’s Drug Delivery Devices Symposium, taking place on the 10th of March, 2021. Attendees should not miss out on panel discussions on critical topic areas such as International Perspectives on Regulatory Pathways & Device Design and Engineering.

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Pharmacy Joe

FEBRUARY 19, 2023

In this episode, I’ll discuss topical lidocaine for wound VAC dressing changes. Episode 793: Topical lidocaine for wound vac dressing changes Subscribe on iTunes , Android , or Stitcher Vacuum-assisted closure of wounds uses a device to decrease air pressure on a wound and allow it to heal faster.

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FDA Law Blog: Biosimilars

NOVEMBER 30, 2023

The speaker faculty of top FDA regulatory authorities will share critical insights on foreign and domestics inspections, digital health, DOJ’s compliance guidelines, and data privacy, among many other topics. The conference will also include its annual panel discussion with FDA’s Center Compliance Directors.

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Communication 59

European Pharmaceutical Review

MAY 2, 2023

The US Food and Drug Administration (FDA) has released a new draft guidance to further support the use of decentralised clinical trials (DCTs) for drugs, biologics and devices. The FDA’s regulatory requirements for investigations of medical products are the same for DCTs and traditional site-based clinical trials.

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Packaging 86

FDA Law Blog: Biosimilars

JUNE 22, 2023

Mullen — FDA has been clearing over-the-counter (OTC) in vitro diagnostic (IVD) tests nearly since the beginning of its premarket regulation of devices. Companies are also experiencing significant regulatory obstacles with another related category: home collection devices. Cato & Jeffrey N. Gibbs & Allyson B.

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Labelling Hospitals 59

PharmaShots

MAY 5, 2023

The expo is targeting medical and healthcare tech's brightest brains and thought leaders in the middle east and around the world. The key takeaways from the event are: Gain insights and understanding of where the medical sector is heading in the near future. Meet and connect with industry peers to collaborate in future endeavors.

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RX Note

JULY 16, 2023

tanning beds, phototherapy devices). Although topical corticosteroids are frequently used in clinical practice , there is little evidence that they are beneficial in reducing the symptoms and healing time of sunburn. Painful erythema starts 2 to 6 hours after exposure , reaching a maximum at 24 hours.

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Mayo Clinic 52

The Digital Apothecary

JANUARY 23, 2021

How do we get Digital Health into Medical Education? I have given multiple international and national talks on this topic and serve as a thought leader and subject matter expert on engaging digital health in education for the upcoming future of patient care. Second, how do we integrate digital health into medical education?

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Pharmaceutical Technology

JUNE 12, 2023

Patients with erectile dysfunction (ED) will now be able to access a topical treatment without the need for a prescription after the US Food and Drug Administration (FDA) greenlit Futura Medical’s Eroxon. Shares in Futura Medical rose following the FDA nod – opening 28% higher than the previous day’s (June 9) close.

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pharmaphorum

MARCH 15, 2022

Using information garnered from hundreds of patient sessions conducted by leading pharmaceutical and medical device companies, Within3 recommends five best practices for asynchronous virtual patient engagement: Choosing the right participants – both patients and moderators. Tips for conducting blind or double-blind sessions.

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Express Pharma

JANUARY 21, 2024

He highlighted initiatives like bulk drug and medical device perk schemes, common facility support, and a dedicated policy framework presently mapping the value chain across tariffs and GST to optimise tax structures and incentivise domestic value addition.

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FDA Law Blog: Biosimilars

OCTOBER 10, 2023

By Philip Won & Véronique Li, Senior Medical Device Regulation Expert — As we recently blogged , FDA released three draft guidance documents to help enhance the predictability, consistency, and transparency of the 510(k) program. One of these documents focuses on “ Evidentiary Expectations for 510(k) Implant Devices.”

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pharmaphorum

NOVEMBER 17, 2021

SMi Group’s 14 th Annual Conference and Exhibition: Pre-Filled Syringes and Injectable Drug Devices 2022 – 12 th – 13 th January 2022. Sustainability for Drug Devices Focus Day – 14 th January 2022. The Future of Drug Delivery and Combination Product Device Design. London, UK www.pre-filled-syringes.com/Pharmaphorum.

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pharmaphorum

SEPTEMBER 4, 2020

Topics of discussion will include the latest updates on the EU MDR and Article 117, advances in novel drug products and biologics, parenteral packaging for pre-filled syringes, innovations in device design and platforms for combination products, lifecycle management and much more…. Pre-Filled Syringes and Injectable Drug Devices.

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Packaging 52

Viseven

NOVEMBER 17, 2022

Medical affairs in Pharma are often seen as a central agency that works within a healthcare company and prioritize communication among life science organizations, medical professionals, healthcare providers, and patients. What are pharmaceutical medical affairs? . What do medical affairs teams do? .

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Pharma Packaging Solutions

SEPTEMBER 26, 2019

We have plenty of new things to talk about including sustainable packaging – this seems to be a hot topic and we are your sustainability packaging partner. And the always hot topics of serialization and aggregation are open for discussion. If you need to kit or carton a medical device, we are also happy to help you.

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RX Note

AUGUST 4, 2023

Introduction Pharmaceutical care has been defined as medication-related care provided through direct patient contact and intended to improve quality of life. In United States, concerns regarding improper medication use led to mandates requiring pharmacists to provide patient counselling and education (e.g. For device counselling (e.g.

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Patient Counseling Communication Inpatient Diabetes 52

FDA Law Blog: Biosimilars

JUNE 20, 2023

By Véronique Li, Senior Medical Device Regulation Expert & Allyson B. Mullen — On June 2, 2023, FDA issued the latest version of its guidance on Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program.

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RX Note

MARCH 1, 2023

Pharmaceutical Care Pharmaceutical care has been defined as medication-related care provided through direct patient contact and intended to improve quality of life. In United States, concerns regarding improper medication use led to mandates requiring pharmacists to provide patient counselling and education (e.g.

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Patient Counseling Diabetes 52

pharmaphorum

AUGUST 31, 2022

Futura Medical’s development of a topical treatment for erectile dysfunction (ED) is approaching the finish line in the US, as the UK biotech reports confirmatory phase 3 data ahead of an FDA filing later this month. ” The post Futura eyes FDA filing as topical ED drug passes phase 3 test appeared first on.

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FDA Law Blog: Biosimilars

NOVEMBER 2, 2023

Lewis, Senior Regulatory Device & Biologics Expert — On October 20, 2023, FDA announced the availability of the final guidance authored by CBER titled “Voluntary Consensus Standards Recognition Program for Regenerative Medicine Therapies.” Tobolowsky & Richard A. It finalized a draft guidance published in 2022.

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Express Pharma

AUGUST 2, 2023

For seeking healthcare-related information, seven out of 10 people will search the internet, similarly for medical information. What is the audience mix for the GDHS 2023 and what can they expect in terms of speakers, topics, masterclasses, actionable insights etc? We are discussing solutions to implement.

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Pharmaceutical Technology

JUNE 10, 2023

Its product portfolio includes pharmaceutical products such as anti-allergic agents, anti-tumor agents, H2 receptor antagonists, antibiotics and medical devices; and consumer health products such as herbal digestive medicine, topical analgesics, antifungal cream and herbal medicine powder, among others.

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Drug Development 40

Pharmaceutical Technology

JUNE 10, 2023

Its product portfolio includes pharmaceutical products such as anti-allergic agents, anti-tumor agents, H2 receptor antagonists, antibiotics and medical devices; and consumer health products such as herbal digestive medicine, topical analgesics, antifungal cream and herbal medicine powder, among others.

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Pulses

JUNE 13, 2023

They can provide insight into how this topic is currently covered in the content and where/how it could be better covered in the curriculum. 4,5 Gather Input from External Stakeholders Do alumni feel the topic was covered? What were perceptions of the breadth and depth of the topic? Was the pedagogical approach effective?

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PharmaShots

JANUARY 23, 2023

Until recently, there were very few topical options available for treating plaque psoriasis long-term. Typically, some patients start with topical steroids; however, these can be challenging, as many are limited by where they can be applied on the body and for how long and how often they can be used. [i] of VTAMA cream?

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National Association of Boards of Pharmacy

JULY 19, 2023

In pharmacy, AI could be used to help automate routine and traditionally manual tasks that might include ordering, verifying, dispensing, and even administering medications, for example. AI could also provide an elevated level of support for pharmacists and other clinicians across many aspects of medication therapy.

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Putting Patients First Blog

FEBRUARY 22, 2024

On topics such as artificial intelligence and ‘the new normal’ in health care, attendees are collaborating to create the next generation of first-class, patient-centered care.” “The She will share highlights from the IS 2023 Health of the Sector Report and provide her perspective on the workforce challenges facing non-profits.

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