Alta Sciences

NOVEMBER 4, 2024

Download a copy of this case study. Product Disposal: We disposed of all waste and material generated from the manufacturing loteprednol etabonate at regulated chemical treatment facilities. Loteprednol etabonate, a corticosteroid, requires stringent safety protocols due to its classification as a highly potent API.

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Engineering Production Compliance Laboratories 52

Agency IQ

MARCH 15, 2024

California publishes draft regulations for landmark plastic pollution reduction act CalRecycle has launched the formal rulemaking process for Senate Bill 54, which will implement a sweeping plan to reduce plastic waste in the state by 2032. However, a producer may also choose to apply for independent compliance with the requirements.

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PPD

JULY 16, 2024

Staying current with PV-relevant regulations and regulatory guidance can be challenging and often requires an FSP PV RI team that spans multiple countries and languages. Download the white paper The post Expert Interpretation and Analysis of Regulatory Intelligence Are Key to FSP-Delivered Pharmacovigilance appeared first on PPD.

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Compliance Regulations Production Trials 98

Agency IQ

AUGUST 9, 2024

Commission proposes exemptions to UV-328 ban under POPs Regulation The European Commission plans to implement exemptions introduced under the Stockholm Convention’s 2023 ban of UV-328, an ultraviolet-light absorbing persistent organic pollutant (POP). This exemption is in accordance with Article 4(1)b of the POPs Regulation.

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Regulations Production International Marketing 40

The Pharma Data

SEPTEMBER 15, 2020

Regulation in biotech can be both a barrier and a solution for innovating the drug discovery process as the pharma industry shifts from blockbuster products toward new individualized forms of medicine. Download Your Copy. Balance risk and innovation in regulation using new digital-therapy products. Add bookmark.

Regulations 52

Regulations Production Therapies Treatment 52

Perficient: Drug Development

JUNE 4, 2024

Compliance : For organizations operating in regulated industries or regions with strict compliance requirements, self-hosted runners offer greater control and visibility over where code is executed and how data is handled, facilitating compliance efforts. zip", "$PWD") Configure the runner using the below command.

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Compliance Packaging Regulations 105

The Pharma Data

JANUARY 6, 2021

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you agree to having your details passed onto the sponsor who may promote similar products and services related to your area of interest subject to their privacy policy. . Meet compliance regulations and conductivity measurements.

Compliance 52

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The Pharma Data

JANUARY 13, 2021

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you agree to having your details passed onto the sponsor who may promote similar products and services related to your area of interest subject to their privacy policy. . Meet compliance regulations and conductivity measurements.

Compliance 52

Compliance Regulations Production Pharmaceuticals 52

Fierce BioTech

OCTOBER 2, 2023

Logistics For Cell & Gene Therapy Trials: Specific Needs Demand Special Skills Download now to learn more about intricate trial logistics, the importance of expertise, navigating regulations, secure data management, and real case studies like viral vector therapy for Spinal Muscular Atrophy. A specialized provider is essential.

Therapies 52

Therapies Trials Regulations Disease 52

PPD

FEBRUARY 10, 2025

By harnessing the full range of innovative technologies and taking advantage of an FSP partners extensive skills and experience, sponsors are able to bring their therapies to market more quickly and within budget even in the face of complicated global regulations and widely fluctuating workloads.

Clinical Trials 52

Clinical Trials Trials Clinical Research Research 52

The Pharma Data

SEPTEMBER 9, 2020

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you will receive our e-newsletter, including information on Podcasts, Webinars, event discounts, online learning opportunities and agree to our User Agreement. . Download Your Copy.

Production 52

Production Laboratories Compliance Government 52

The Pharma Data

SEPTEMBER 1, 2020

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you will receive our e-newsletter, including information on Podcasts, Webinars, event discounts, online learning opportunities and agree to our User Agreement. Download Your Copy. Download Your Copy.

Clinical Trials 52

Clinical Trials Trials Regulations Production 52

Drug Channels

OCTOBER 23, 2023

With regulation and policy changes, specifically surrounding the DCSCA, IRA and serialization, the loss of exclusivity wave, adoption of low-WAC products affecting GTN and the rise of alternative distribution models, there has never been a more important time for industry to unite. Why should you attend this pivotal event?

Pharmacy 75

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Drug Channels

JANUARY 22, 2021

These solutions promote interoperability and help healthcare businesses meet regulations related to health information exchange. To learn more, download the Wolters Kluwer interoperability stories ebook. Jason discusses the benefits of accessing patient information across clinical contexts. Read on for Jason’s insights.

Regulations 52

Regulations Production Drugs 52

PPD

DECEMBER 16, 2024

Each region presents its own set of unique and complex regulations that must be met, creating a daunting landscape for companies striving to bring their therapies to market. Although adhering to complex regulations may initially complicate trials, it serves as a critical safeguard against future roadblocks.

Drug Development 52

Drug Development Clinical Trials Compliance Trials 52

PPD

AUGUST 16, 2023

Fortunately, leading global regulators have launched key initiatives. Clinical investigators, physicians, payers, regulators and certainly patients have their interests, such as quality of care, cost reduction and convenience. Explore the perspectives of clinicians executing hybrid and DCT models.

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Clinical Trials Trials Clinical Research FDA 98

The Pharma Data

DECEMBER 15, 2020

Download the whitepaper at: [link]. Our combined experience cuts across most industries with a specialization in US FDA Quality System Regulations and ISO 13485:2016 Quality Management System Requirements. # # #. Source link.

Science 52

Science Compliance Regulations FDA 52

The Pharma Data

NOVEMBER 6, 2020

Download Your Copy. We respect your privacy, by clicking “Download Your Copy” you will receive our e-newsletter, including information on Podcasts, Webinars, event discounts, online learning opportunities and agree to our User Agreement. Download Your Copy. Add bookmark.

Production 40

Production Pharmaceuticals Regulations 40

ACTO

OCTOBER 22, 2024

Compliant: Designed to comply with FDA regulations. So how can such a knowledge assistant be successfully implemented and accepted in our highly regulated industry? To learn how to build a successful GenAI Knowledge Assistant Pilot Program, download this guide. Secure: Certified to protect data privacy and security.

Science 52

Science Regulations FDA Compliance 52

H1 Blog

NOVEMBER 15, 2023

But in today’s highly regulated environment, it is more important than ever to make sure that HCP engagement plans are compliant with anti-kickback laws. However, with strict regulations surrounding interactions between industry and healthcare professionals, compliance must be at the forefront of any KOL engagement plan.

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Compliance Science Regulations Pharmaceutical Companies 59

Perficient: Drug Development

OCTOBER 3, 2024

Support and Compliance: Upgrading ensures continued support from HCL and compliance with industry standards and regulations. Download and extract the Update Package that you want to install. xx To upgrade, HCL Commerce Developers first need to download the HCL Commerce Enterprise Developer from the HCL Flexnet portal.

Packaging 52

Packaging Compliance Licensing Licensing 52

Perficient: Drug Development

SEPTEMBER 26, 2024

Support and Compliance: Upgrading ensures continued support from HCL and compliance with industry standards and regulations. Download and extract the Update Package that you want to install. Installation Step: To upgrade HCL Commerce Developer first need to download the HCL Commerce Enterprise Developer from HCL Flexnet portal.

Packaging 52

Packaging Compliance Licensing Licensing 52

Drug Channels

NOVEMBER 30, 2020

Staying on the pulse of industry trends, policies and changing regulations has never been more crucial. With drug pricing and benefit coverage top of mind for many Americans, coupled with a volatile election and overall healthcare landscape, the stakes are incredibly high for bio/pharma manufacturers.

Government 52

Government Pharma Companies Regulations Drugs 52

Perficient: Drug Development

OCTOBER 7, 2024

However, the new lengthy regulation raised many questions by the industry, and Perficient’s Financial Services Risk and Regulatory consultants have been researching answers and questioning regulators to provide in order to provide our current and future clients the answers to the following questions that have been raised.

Compliance 52

Compliance Regulations Research 52

Drug Channels

SEPTEMBER 3, 2024

Download the brochure. The Healthcare Innovation Company's Value-Based Care Summit In-Person Event | October 28 - 29, 2024 in Washington, DC Use promo code VBCDC to save $100. Register Today.

Pharmaceutical Companies 52

Pharmaceutical Companies Pharmaceuticals Government Regulations 52

The Pharma Data

JANUARY 25, 2021

Maypharm is focusing on outstanding pharmaceutical products to provide superior botulinum toxin product with an up-to-date technological advantage and elaborated advanced manufacturing quality system and sophisticated equipment to meet the GMP requirements of the Agency’s CGMP regulations. For more information visit www.maypharm.net.

Production 52

Production Clinical Trials Marketing Regulations 52

Perficient: Drug Development

DECEMBER 22, 2023

This personalized approach ensures that individuals facing psychiatric disabilities receive immediate and tailored support, promoting emotional regulation and coping strategies. The AI companion engages users in guided conversations, implementing evidence-based therapeutic techniques.

Regulations 52

Regulations Therapies Production 52

Perficient: Drug Development

SEPTEMBER 27, 2023

including phone calls, app downloads, and in-app purchases, among others. In summary, Enhanced Conversions addresses the challenges posed by privacy regulations and limited access to third-party information. With Enhanced Conversions, advertisers can capture and measure various types of conversions beyond standard website conversions.

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Regulations Compliance Marketing 52

Perficient: Drug Development

OCTOBER 5, 2023

Emotional Regulation : Sensory integration apps can assist in regulating emotions and reducing anxiety or sensory overload, enabling individuals to cope with challenging situations more effectively.

Regulations 52

Regulations Therapies Production Disease 52

The Pharma Data

DECEMBER 21, 2020

.” Kaiser Permanente’s elimination of member out-of-pocket costs applies to all fully insured benefit plans, in all markets, unless prohibited or modified by law or regulation. View original content to download multimedia: [link]. Media Contact: Marc Brown marc.t.brown@kp.org 510-407-2592. Source link.

Virus 52

Virus Clinical Research Treatment Disease 52

The Pharma Data

DECEMBER 27, 2020

. This information is information that C-RAD AB (publ) is obliged to make public pursuant to the EU Market Abuse Regulation. The following files are available for download: View original content: [link]. This information was brought to you by Cision [link].

Treatment 52

Treatment Therapies Regulations Marketing 52

Drug Channels

AUGUST 14, 2021

Exclusive Offer – Download the agenda and register today – Be sure to use your exclusive promo code USAVE10 to save 10% off* of your registration. Analyze State and Federal Progress Regulating Copay Programs DOJ Updates:?Government 2021 is a must-attend. Whether you choose to attend in-person or virtual (or both!)

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Government Regulations Therapies Drugs 40

The Pharma Data

OCTOBER 25, 2020

” This disclosure contains information that RhoVac is obliged to make public pursuant to the EU Market Abuse Regulation (EU nr 596/2014). The following files are available for download: View original content: [link]. The information was submitted for publication, through the agency of the contact person, on 26-10-2020 08:30 CET.

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Regulations Disease Marketing 40

FDA Law Blog: Biosimilars

MARCH 7, 2023

Lenz, Principal Medical Device Regulation Expert — As we discussed in our prior post , the electronic Submission Template And Resource (eSTAR) template will take getting used to in terms of form. It must first be downloaded, revised, and uploaded back to the system. By Adrienne R.

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FDA Regulations 59

Crucial Data Solutions

MAY 31, 2023

Improvements to data collection technologies and processes, a robust high-speed internet infrastructure, and pressure from regulators to make research more inclusive are converging, making exclusively site-based study designs increasingly rare. Clinical trials continue to move closer to patients. Luckily, there is one solution.

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Clinical Trials Trials Compliance Research 52

Advarra

JUNE 14, 2024

Though not legally binding, maintaining a regulatory binder is highly recommended for all intervention trials. This checklist offers a comprehensive framework for managing all necessary documents efficiently.

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Clinical Trials Trials Compliance FDA 40

The Pharma Data

NOVEMBER 1, 2020

This is information that Hansa Biopharma AB is obliged to make public pursuant to the EU Market Abuse Regulation. The following files are available for download: View original content: [link]. This information was brought to you by Cision [link]. SOURCE Hansa Biopharma AB.

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