XTalks

JANUARY 20, 2022

Life science consulting can be a rewarding career and the job outlook is promising for the future. . Perhaps you have heard of life science consulting jobs but do not exactly know what type of work is involved, or the education and experience needed to become a life science consultant. Job Description.

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pharmaphorum

OCTOBER 12, 2022

Remaining compliant is imperative to the life sciences industry, so adhering to regulatory requirements is mandatory. Prior to selling drugs or medical products in any country, pharmaceutical companies must prove compliance and gain the regulatory approval required by the country in which the goods will be distributed in.

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XTalks

FEBRUARY 22, 2022

A successful life science webinar engages the audience in a unique manner, drives the right kind of traffic and provides genuine value for attendees. Here are 5 trending life science webinar topics that have been resonating well with our audiences. Then view our past life science webinars here.

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Cloudbyz

MARCH 17, 2024

In the dynamic world of life sciences, where innovation is paramount, the integration of cutting-edge technologies is crucial for accelerating clinical operations and driving breakthroughs in healthcare. Salesforce’s recent announcement of its Life Sciences Cloud marks a significant stride towards this goal.

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pharmaphorum

FEBRUARY 4, 2021

However, issues like compliance, governance and security often are. That’s why CIOs and CTOs working within the life sciences industry need to include Salesforce org management as a key component of their standard operating procedures. This will help ensure consistency and compliance across the entire enterprise. .

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pharmaphorum

APRIL 27, 2017

The life sciences landscape is moving at a rapid pace, which in turn is increasing the demands on marketers to create innovative, digital content faster while maintaining industry compliance. Veeva Systems recently conducted an annual industry study, focused on content and digital asset management within life sciences.

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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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Pharma Times

NOVEMBER 8, 2022

ProductLife becomes partner in upholding regulatory and compliance across life sciences

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pharmaphorum

JANUARY 6, 2023

From enabling patient choice during clinical trials to strengthening vital partnerships across the quality ecosystem, connected data will become the lifeblood that enables life sciences teams to collaborate efficiently and effectively in 2023. The post 6 research and development life sciences predictions for 2023 appeared first on.

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XTalks

SEPTEMBER 13, 2023

Claudia Grimaldi is currently Vice President, Principal Finance Officer, and Chief Compliance Officer at IGC. She has been with the company for almost 12 years with increasing responsibilities including managing SEC and NYSE filings, regulatory compliance and disclosures.

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Pharmaceutical Commerce

MAY 8, 2023

How maximizing the value of compliance data can help drive commercial decisions.

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Cloudbyz

DECEMBER 22, 2024

Cloudbyzs dual recognition underscores its commitment to innovation , regulatory compliance, and enhanced trial efficiency. As life sciences organizations increasingly seek digital transformation , Cloudbyz continues to deliver solutions that simplify workflows and accelerate drug development timelines.

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XTalks

DECEMBER 9, 2024

The draft also formalizes withdrawal procedures for non-compliance, including delayed studies or failure to confirm benefits. Notably, the FDA can now mandate that confirmatory trials begin before approval, ensuring proactive validation of clinical benefits.

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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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FDA Law Blog

JULY 30, 2024

By Sara M Keup & Véronique Li, Senior Medical Device Regulation Expert — The American Conference Institute (“ACI”) held its 11th Annual Summit for Women Leaders in Life Sciences Law at the Seaport Hotel in Boston, Massachusetts on July 25th & 26th of last week. GLP-1s – Exploring the Anticipated Compliance and Litigation Risks.

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Intouch Solutions

AUGUST 5, 2024

It works because it’s been designed from the ground up for life sciences. TEDAVI uses robust methodologies, cutting-edge platforms and AI-driven capabilities to help clients overcome regulatory challenges, reduce costs, streamline creation and review, and enable personalization – all while maintaining compliance.

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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. Its acquisitions and integrations have been carefully calculated and culminated into a life sciences powerhouse that helps clients solve critical and complex challenges.

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Cloudbyz

SEPTEMBER 11, 2024

This prestigious recognition positions Cloudbyz among the top performers in delivering intuitive and scalable EDC solutions to life sciences organizations worldwide. This prestigious recognition positions Cloudbyz among the top performers in delivering intuitive and scalable EDC solutions to life sciences organizations worldwide.

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pharmaphorum

OCTOBER 29, 2015

Findings from the Veeva 2015 European Life Sciences Survey Is the industry getting what it needs? Customer data challenges are among the most vexing and pervasive that life sciences companies currently experience, especially with the increasing regulatory pressure and the transition to new business models they face.

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Cloudbyz

APRIL 12, 2023

UCTMS also helps organizations ensure compliance with regulatory guidelines and provides robust data security features. By automating these processes, Cloudbyz CTMS helps life sciences companies conduct clinical trials more efficiently. These features help life sciences companies remain compliant and avoid costly fines.

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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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Cloudbyz

AUGUST 13, 2024

In the rapidly evolving landscape of life sciences, the need for robust, efficient, and compliant pharmacovigilance (PV) solutions has never been greater. In this blog, we’ll explore how these solutions are transforming pharmacovigilance and why they are becoming the go-to choice for forward-thinking life sciences companies.

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BioTech 365

APRIL 5, 2021

Porzio Life Sciences Launches Porzio GST, U.S. and Global Transparency Solution for the Life Sciences Industry Porzio Life Sciences Launches Porzio GST, U.S. and Global Transparency Solution for the Life Sciences Industry MORRISTOWN, N.J.–(BUSINESS

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XTalks

DECEMBER 20, 2023

In 2023, there were significant advancements and notable trends in the life sciences. Xtalks compiled a list of its top life science news and trends of 2023, which provided readers with the latest developments, information and expert insights across life science industries, including pharma, biotech and medical device.

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Outsourcing Pharma

APRIL 11, 2023

OSP spoke to Vladamir Penkrat, head of safety and regulatory and Shuba Rao a senior director at Indegene, a life sciences digital company about a paper they recently published called 'Challenges and Future of PV Compliance' about the direction compliance is headed and how they would convert risk-based approaches into a confidence-based assurances. (..)

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XTalks

JULY 9, 2024

In the dynamic landscape of clinical trials, ensuring compliance and maintaining high-quality standards are paramount. The field of quality and compliance in clinical trials is undergoing significant transformations driven by technological advancements, regulatory changes and evolving industry practices.

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FDA Law Blog

NOVEMBER 30, 2023

The 2023 Food and Drug Law Institute’s (“FDLI”) Enforcement, Litigation and Compliance Conference will boast two speakers from Hyman, Phelps & McNamara, P.C. (“HPM”), HPM Director Anne Walsh will moderate a panel discussion on “Due Diligence and Mitigating Securities Violation Risks for Emerging Life Science and Novel Food Companies.”

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Pharma Marketing Network

APRIL 21, 2021

Darshan Kulkarni and Marc Banjak, General Counsel at Dova Pharmaceuticals, discuss sales compliance in the life sciences. Sales and marketing representatives in the life science industry must comply with state and federal regulations. What are these regulations and how should you navigate them?

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Cloudbyz

MARCH 30, 2023

In today’s digital age, life sciences organizations are collecting, storing, and processing vast amounts of sensitive data, including personally identifiable information (PII) and protected health information (PHI). As such, it’s becoming increasingly challenging for organizations to manage and secure this data.

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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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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. Increase study quality and compliance. Add bookmark. Download Your Copy. Download Your Copy.

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Cloudbyz

MARCH 28, 2023

This solution is designed to meet the unique needs of clinical research organizations (CROs) and pharmaceutical companies, offering a range of features to help them streamline their operations, manage clinical trials, and ensure compliance with regulatory requirements.

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The Pharma Data

DECEMBER 15, 2020

FAIRFAX, VA, December 15, 2020 /24-7PressRelease/ — Quality and Regulatory Compliance requirements can present impediments to progress. However, these requirements also reveal opportunities to re-envision a team’s effectiveness, renovate processes, and enable newer technologies to revamp business-as-usual.

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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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Pharmaceutical Commerce

MARCH 27, 2025

In the final part of his video interview with Pharma Commerce Editor Nicholas Saraceno, Brad Stewart, BDOs national life sciences co-leader, details the Biosecure Act, including the ways pharma companies are preparing for it, especially from a compliance standpoint.

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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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pharmaphorum

MARCH 15, 2022

Life science companies invest a significant number of resources to engage physicians and patient advocates. In a new whitepaper, Best Practice Guide: Insights Management and Virtual Patient Engagement, Within3 provides a detailed roadmap to help life science companies navigate engagement in the virtual world.

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