pharmaphorum

FEBRUARY 23, 2021

Life sciences organizations can easily send customizable, templated text messages and digital assets without compromising compliance. We have experienced significant demand for our text messaging platform within the life sciences industry,” stated Arist Co-founder and CEO Michael Ioffe. “To Onboarding and Training.

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XTalks

JULY 5, 2022

Employee retention and motivation is a challenge that all life science companies face. A corporate compliance training program is a part of many onboarding programs to ensure employees are up to date with the latest rules and regulations they must adhere to while working for the company. Training and Development Opportunities.

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Cloudbyz

JUNE 10, 2023

21 CFR Part 11 is a crucial component of regulatory compliance in clinical trials and, more broadly, any industry subject to the regulations of the U.S. This blog post will serve as a comprehensive guide to understanding and implementing 21 CFR Part 11 compliance in your clinical trials. Food and Drug Administration (FDA).

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The Pharma Data

DECEMBER 8, 2020

Find out what 500 global clinical operations professionals had to say as they shared their experiences and opinions on the progress of modernizing clinical operations in life sciences. Add bookmark. Download Your Copy. Achieve real-time, end-to-end visibility and oversight of clinical trial processes.

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The Pharma Data

MARCH 20, 2021

Natural language processing (NLP) has long held potential for the life sciences field, given the industry’s reliance on text-based data in the form of clinical records, scientific papers, pharmaceutical companies’ call center transcriptions and so forth. Reed, director of life sciences at Linguamatics, an IQVIA company. “To

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Pharmaceutical Technology

AUGUST 30, 2022

Verista is a Life Sciences business, technology and compliance firm specializing in systems, quality, and validation solutions throughout the product lifecycle. Verista is a leading life sciences business, technology and compliance company that enables clients to improve health and improve lives.

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Cloudbyz

OCTOBER 25, 2023

SPAR Solutions provides agile, innovative solutions to help clients leverage the Salesforce platform as their primary business engine The joint partnership, powered by Cloudbyz ’s Clinical Research Management Platform and SPAR Solutions, holds immense promise for the healthcare and life sciences sectors.

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Pharma in Brief

DECEMBER 3, 2023

This year marks the 30-year anniversary of the Patented Medicines (Notice of Compliance) Regulations ( Regulations ), introduced in 1993 to prevent patent infringement by linking the regulatory approval of generic or biosimilar drugs with the patent rights of innovators. Full actions (2017–present). 3d) 209 (FCA), at paras.

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Intouch Solutions

AUGUST 1, 2024

With the proven success to save on average 48% production time from traditional agency models, TEDAVI meets the dynamic needs of the pharmaceutical and life science industries. To learn more, visit [link] About EVERSANA® EVERSANA® is a leading independent provider of global services to the life sciences industry.

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Pharma Marketing Network

DECEMBER 12, 2023

Upcoming Informa Connect Events: Speaker Programs Summit – February 26-28, 2024 Event Name: Rare Disease Summit – March 19-21, 2024 PAP – Patient Assistance & Access Programs – March 19-21, 2024 Hub and Specialty Pharmacy Models East – March 19-21, 2024 Pharma Forum – March 24-27, 2024 Pharmaceutical Compliance Congress (..)

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Cloudbyz

MARCH 17, 2023

Life science companies conducting clinical trials must adhere to GCP guidelines to ensure the safety and well-being of study participants and maintain the integrity of the clinical trial data. In this blog post, we will explore the types of alerts on GCP violations that life science companies conducting clinical trials should set up.

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pharmaphorum

JANUARY 25, 2023

Life sciences marketing has rapidly evolved to mirror that of consumer retail. It may not be surprising that the key to customer engagement optimisation, like many other processes within life sciences operations, is orchestrated data management and analysis. Automatic HCP segmentation HCPs change segments regularly.

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pharmaphorum

JUNE 10, 2021

The latest version of the PRISYM 360 cloud-based labeling solution has achieved certification for the GS1 standards utilized by the medical device and life science industries. GS1 oversees a system of globally recognized open standards for unique identifiers that can be used throughout the supply chain to enhance traceability.

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pharmaphorum

MARCH 15, 2022

Life science companies invest a significant number of resources to engage physicians and patient advocates. However, companies often fall short when it comes to engaging patients in a meaningful way during the product development process. Choosing the right questions to prompt robust discussion. How to maintain confidentiality.

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XTalks

FEBRUARY 21, 2022

BioNTech announced its new vaccine manufacturing approach in Africa where the company will ship modular factories, called the BioNTainer, to the continent to enable domestic production of the vaccines to help increase supplies. Related: BioNTech to Build First mRNA Vaccine Production Plant in Africa. Photo source: BioNTech.

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Advarra

SEPTEMBER 14, 2023

GxP in Clinical Trials To yield the best possible outcomes for clinical trials, GxP guidelines and compliance regulations assures regulatory agencies the safest and most productive research efforts are being delivered to the market. In more serious instances, sponsors might see their products recalled entirely.

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Cloudbyz

OCTOBER 25, 2023

The joint partnership, powered by Cloudbyz ’s Clinical Research Management Platform and SPAR Solutions, holds immense promise for the healthcare and life sciences sectors. Together we aim to tackle the foremost challenges in the life sciences industry: timelines, productivity, and compliance.

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pharmaphorum

MAY 18, 2021

A product launch success determines 81% of a drug’s sales performance. Still, research also suggests that many companies are not optimising their strategies for this crucial period: 67% of products fail to meet launch expectations and sales forecasts, and 70% continue to lag behind three years post-launch. “But ” says Hale.

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Cloudbyz

SEPTEMBER 5, 2024

In the ever-evolving landscape of the life sciences industry, ensuring drug safety is paramount. The right solution can streamline operations, ensure compliance, and ultimately safeguard patient well-being. The right solution can streamline operations, ensure compliance, and ultimately safeguard patient well-being.

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pharmaphorum

JANUARY 4, 2022

“Working closely with Zebra engineering teams, we have tested the interoperability of PRISYM 360 with select products, including the ZT400, ZT600 and Xi4 printers that are extensively used by many of our customers,” said Chris Lentz, VP Cloud Platform, PRISYM ID. About PRISYM ID. Media Contact: Andrew Baud, Distil,?

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FDA Law Blog

MARCH 6, 2024

The American Conference Institute (“ACI”) will be hosting a series of go-to forums on critical topics including novel therapeutics, cosmetics/personal care products and Paragraph IV disputes. Claud will be featured at the Legal, Regulatory, and Compliance Forum on Cosmetics & Personal Care Products in New York, NY.

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Drug Channels

MARCH 6, 2023

Experts from across the industry will discuss how current and future drug pricing transparency regulations will impact commercialization, reimbursement, pricing and compliance practices. Plus, assess how companies are internally planning for these changes.

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pharmaphorum

OCTOBER 19, 2022

Emma Hyland, VP strategy, commercial content at Veeva Systems, tells us modular content is the most significant wave of innovation hitting the content world in life sciences, and rightly so because HCPs’ needs and expectations have changed. “There isn’t a one-size-fits-all for how the life sciences industry creates content.

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pharmaphorum

NOVEMBER 17, 2020

However, the implementation of these while maintaining compliance with internal company guidelines can prove challenging and can be difficult to navigate without support and guidance. Gareth Powell is a business development officer for the NIHR Clinical Research Network (CRN). Gareth has been with the Clinical Research Network since 2009.

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Clinical Trial Podcast

JULY 31, 2022

He is currently the Principal Attorney of Kulkarni Law Firm where he focuses his practice on providing healthcare companies with legal, compliance, and regulatory advice. Last but not the least he is the host of the DarshanTalks livestream interviews where he discusses issues that impact the life science industry.

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pharmaphorum

DECEMBER 7, 2020

Wokingham, United Kingdom — 7 December 2020 — PRISYM ID, a leading provider of regulated content and label management solutions for the life sciences sector, announced today that PRISYM 360 version 1.10 All other product and service names mentioned are the trademarks of their respective companies. www.prisymid.com.

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pharmaphorum

OCTOBER 5, 2020

In his new role, Amresh will be responsible for overseeing and coordinating the people, resources and processes required to deliver new solutions and upgrade existing products, primarily around the PRISYM 360 regulated labeling platform for clinical trials supplies and medical device manufacturers. www.prisymid.com. For more information:? .

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pharmaphorum

SEPTEMBER 29, 2022

The FDA’s General Approach to Regulating mHealth Products. Although mHealth has been gaining in popularity for at least the past decade, before commercializing their mHealth products, developers must determine whether the product is subject to U.S. General Wellness Products. Mobile Medical Applications.

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XTalks

APRIL 21, 2023

It highlights the importance of ethical standards, due diligence and regulatory compliance, and underscores the potential risks associated with over-hyped or fraudulent startups. Life science startups face unique challenges given the highly regulated and complex nature of the industry.

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pharmaphorum

FEBRUARY 4, 2021

Adams believes this positive start to the year is a sign that life science and medical device companies are looking for expert partners who understand the operational and regulatory challenges facing them and can deliver scalable solutions that meet their unique requirements. “It The challenge now is to lock in these gains.

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Cloudbyz

NOVEMBER 9, 2021

an innovative digital solutions provider for organizations that specialize in Clinical Research, Life Sciences, and Biopharmacy, announces receiving the ISO 9001:2015 certification. CHICAGO , Nov. 9, 2021 /PRNewswire/ — Cloudbyz Inc.,

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Pharma in Brief

SEPTEMBER 5, 2023

On August 8, 2023, the Federal Court overturned Health Canada’s decision that a cannabis product, Edison Jolts, was to be classified as edible cannabis and not cannabis extract. manufactures Edison Jolts ( Jolts ), which are cannabis products in lozenge form. Background Organigram Inc.

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Pharmaceutical Technology

OCTOBER 28, 2022

A key part of this includes the careful selection of personnel for the lay summary production. But if they’re doing that internally, they may have a bias, either because of a life sciences background or involvement in the clinical trial itself.

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pharmaphorum

SEPTEMBER 28, 2021

P360 , a leading developer of technology for life sciences companies, today announced that its ZING Communication Module has been enhanced with several new enterprise-grade unified communication features. The response to ZING from life sciences companies has been strong as well. “We

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pharmaphorum

OCTOBER 27, 2022

The Guidance applies to both product-related and therapeutic-area-related activities. To help ensure compliance, it is advisable for companies to establish procedures to assess and verify IT security of social media and digital channels, and to review and monitor company activities, content, and materials. About the authors.

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pharmaphorum

NOVEMBER 2, 2022

Citeline provides intelligence, data and software for clinical trials, development and regulatory compliance and was formerly part of Informa was called Pharma Intelligence ahead of a rebranding earlier this year.

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pharmaphorum

SEPTEMBER 7, 2020

He will take the lead driving Clinical Trials Sales in the North American market, building on his relationships with pharma and CROs, demonstrating how our market-leading products can be integrated into a clinical trial supply chain to deliver a compliant labeling solution.”. www.prisymid.com.

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