Drug Patent Watch

JANUARY 9, 2025

Take the time to clearly define your technical needs, from drug substance manufacturing to packaging requirements. Industry directories, conferences, and networking can all be valuable sources of information. Work with your CDMO to stay informed about upcoming changes that could impact your project.

Compliance 52

Compliance Drug Development Pharma Companies Therapies 52

Codon

JUNE 5, 2025

pyogenes protein — whose compactness makes them far easier to package into viral vectors and deliver into the human body. This in vivo editing strategy also requires genome editors to be packaged so that they can be delivered to the correct cells in a desired tissue or organ.

DNA 81

DNA RNA Clinical Trials Engineering 81

BioPharma Drive: Drug Pricing

JUNE 24, 2025

Skip to main content CONTINUE TO SITE ➞ Dont miss tomorrows biopharma industry news Let BioPharma Dives free newsletter keep you informed, straight from your inbox. View our other publications | Privacy policy | Terms of use | Take down policy. All copyright resides with them. Informa PLCs registered office is 5 Howick Place, London SW1P 1WG.

RNA 219

RNA Drugs Therapies Licensing 219

BioPharma Drive: Drug Pricing

JULY 14, 2025

Skip to main content CONTINUE TO SITE ➞ Dont miss tomorrows biopharma industry news Let BioPharma Dives free newsletter keep you informed, straight from your inbox. PCI helps biopharmaceutical companies manufacture and package drug products used in clinical trials as well as commercially. All copyright resides with them.

Production 152

Production Drugs Therapies Clinical Trials 152

FDA Law Blog: Drug Discovery

DECEMBER 6, 2024

Because this guidance covers such a breadth of information, for Part 1 of our coverage, we will focus on the non-CMC topics and summarize our top takeaways from each section, something of a Cliffs Notes for the Cliffs Notes. The draft guidance recommends that no more than 15 questions are included in the briefing package.

Therapies 59

Therapies FDA Production Disease 59

FDA Law Blog: Biosimilars

APRIL 10, 2025

While much of the focus has been on how these cuts may impact application review timelines and industry engagement, see earlier post about the effect on generic drugs, another quieter consequence is emerging a significant slowdown in the availability of information that FDA is required to produce under the Freedom of Information Act (FOIA).

FDA 59

FDA Packaging Government International 59

Drug Patent Watch

JANUARY 7, 2025

As healthcare professionals, it’s our responsibility to educate patients about generic drugs and empower them to make informed decisions about their treatment options. Mobile Apps Develop or recommend mobile apps that provide information about generic drugs, compare prices, and offer medication reminders.

Drugs 69

Drugs FDA Doctors Trials 69

Perficient: Drug Development

MARCH 20, 2025

using the command below: This installation generates three key files: A node_modules folder for all your libraries, packages, and third-party code. A package-lock.json file, which will lock down the versions for each package. The actions takes the information that the user provided to each prompt. Once your Next.js

Packaging 52

Packaging Production 52

Perficient: Drug Development

APRIL 2, 2025

Install Required Nuget Packages To enable logging using NLog , install the following NuGet packages: Install-Package NLog Install-Package NLog.Extensions.Logging Install-Package Microsoft.Azure.Cosmos 3. Create and Configure Nlog.config NLog uses an XML-based configuration file to define logging targets and rules.

Packaging 59

Packaging 59

Perficient: Drug Development

MAY 20, 2025

NLP provides significant search relevancy enhancements and includes modern and regularly updated packages. To obtain further information from our award-winning team, please visit [link]. It also has a fast and robust annotator for arbitrary texts, which improves search relevancy. Other Blogs in the Series HCL Commerce V9.1

Packaging 52

Packaging Production Marketing 52

Perficient: Drug Development

APRIL 1, 2025

It allows for delegated access , meaning that users can grant specific, controlled access to their data without revealing their login information. It is used to verify the identity of the user and obtain their profile information. Developer Contact Information : Enter your email address. OAuth2 (Open Authorization 2.0)

Packaging 52

Packaging 52

Drug Patent Watch

MARCH 19, 2025

By conducting a thorough patent landscape analysis, you can: Identify opportunities to strengthen your patent portfolio through re-examination or re-issuance Develop a strategy for defending against generic challenges Inform your product development and lifecycle management decisions Staying Ahead of the Competition In addition to patent management, (..)

Drugs 40

Drugs Packaging Pharmaceuticals Production 40

Codon

JULY 14, 2025

And many who recount medical and scientific histories (or, indeed, any history at all) do so despite incomplete information. Eichengrün noted that it wasn’t just that aspirin was effective with limited side effects, but also that it came packaged as tablets rather than as a powder in a paper bag. Cite: Harrison, S.

Treatment 83

Treatment Laboratories Disease Drugs 83

Drug Patent Watch

FEBRUARY 17, 2025

Step 2: ANDA Filing Generic drug manufacturers submit an Abbreviated New Drug Application (ANDA) to the FDA, which includes detailed information about the proposed generic drug, including its active ingredients, dosage forms, and manufacturing processes. This includes providing clear instructions for use, warnings, and precautions.

Packaging 52

Packaging Drugs FDA Pharmaceutical Companies 52

Perficient: Drug Development

FEBRUARY 11, 2025

Log errors and provide informative messages to the user. Secure API Keys: Store API keys and other sensitive information securely. User Experience: Provide Clear Feedback: Provide clear and informative feedback to the user. Package the Extension: VS Code uses the vsce (Visual Studio Code Extensions) tool to package extensions.

Packaging 52

Packaging Production International 52

The Pharma Data

JUNE 24, 2025

This pilot effort included employee training on circularity principles and identified ways to apply these concepts to manufacturing and packaging. The assessment provided crucial insights that are now informing the next phase of Baxter’s corporate responsibility strategy.

Production 40

Production Government International Packaging 40

Perficient: Drug Development

JANUARY 14, 2025

Rajiv’s session focused on Docker, explaining how it allows developers to package, deploy, and run applications in isolated containers, ensuring consistency across different environments. You made every session not just informative but truly inspiring. A heartfelt thank you to all our incredible speakers!

Packaging 52

Packaging Production 52

FDA Law Blog: Biosimilars

JUNE 26, 2024

Lenz, Principal Medical Device Regulation Expert — FDA recently released a new eSTAR template for device pre-submissions and 513(g) Requests for Information, referred to as PreSTAR. A 513(g) Request for Information is a means of obtaining FDA’s views about the classification and regulatory requirements for a particular device.

FDA 98

FDA Regulations Production Packaging 98

Perficient: Drug Development

JULY 24, 2024

The package allows the import and export of repository contents. You can use packages to install new content, install new features, change event content, and restore saved content for development. What is included in a package is defined using filters. Key Takeaways Content and configurations are bundled using packages in AEM.

Packaging 52

Packaging 52

SCIENMAG: Medicine & Health

FEBRUARY 12, 2024

Including frozen and prepared meals, most packaged snacks, desserts and carbonated soft drinks—but also including more innocuous foods—they are often considered the bane of healthy eating, containing little to no nutrition to fuel healthy bodies. Ultra-processed foods make up more than half the food average Americans eat.

Packaging 76

Packaging 76

The Pharma Data

DECEMBER 10, 2020

Sildenafil, Trazodone Tablets Recalled After Being Packaged Together. 10, 2020 — Sildenafil and trazodone tablets have been recalled by pharmaceutical distributor AvKARE because the drugs were “inadvertently packaged together” when they were bottled by a third-party vendor, according to the company. More Information.

Packaging 52

Packaging Pharmaceuticals Production Drugs 52

PPD

JULY 20, 2023

In clinical research, the role of drug packaging systems cannot be overlooked. Industry guidelines require biopharmaceutical and biotechnology companies to test their pharmaceutical packaging systems, as the systems often experience prolonged and intimate contact with drug products, drug substances and intermediates.

Packaging 52

Packaging Laboratories Pharmaceutical Companies Compliance 52

Perficient: Drug Development

JUNE 11, 2023

To install Docker on an Amazon EC2 instance using the yum package manager, you can follow the steps below: Connect to your EC2 instance using SSH. While installing docker if you faced any issue respond to this blog will try to solve!! Thank you

Packaging 52

Packaging 52

The Premier Consulting Blog

MAY 31, 2023

While the type, number, and design of these studies vary based on product-specific characteristics, IND-enabling packages submitted to the FDA generally include key information about the pharmacology, pharmacokinetics, and toxicology of the product.

Packaging 52

Packaging Pharmacokinetics Small Molecule Clinical Trials 52

The Pharma Data

DECEMBER 22, 2020

Surprise Medical Bills Could Be Reduced by COVID-19 Relief Package. Further Support and Information on COVID-19. Professional. TUESDAY, Dec. 22, 2020 — Measures to reduce surprise medical bills for Americans are included in the COVID-19 relief bill passed by Congress. The main provisions of the legislation would take effect Jan.

Packaging 52

Packaging Hospitals 52

Broad Institute

MARCH 19, 2024

If we aggregate more genetic information, how much more accurate can our PRSs be?” Several people have already used the R package and reported that it generated a much better score than the scores from individual studies,” said Truong. Chan School of Public Health. “If So far, this accessible approach is proving successful.

Disease 136

Disease Research Packaging Hospitals 136

Agency IQ

NOVEMBER 20, 2023

EMA publishes first electronic Product Information as pilot progresses In 2022, the European Commission, Heads of Medicines Agencies and EMA established a common standard for electronic Product Information, or ePI, an electronic representation of information patients usually receive in paper format along with their medicines.

Production 40

Production Packaging Hospitals Regulations 40

Perficient: Drug Development

AUGUST 28, 2023

Imagine each block sharing information, asking for help, and working together smoothly. Introduction to Feign Client: In the world of software, microservices are like building blocks that help make programs more flexible and scalable. But for these blocks to work together, they need to talk to each other effectively.

Packaging 105

Packaging 105

Perficient: Drug Development

MARCH 12, 2024

Applications and technology need to be designed around an understanding of what data is needed to make better-informed, data-driven business decisions. Enterprises should make sure knowledge workers have access to the up-to-date and timely data they will need to run analytics, identify trends, and make informed business decisions.

Production 104

Production Packaging Engineering Science 104

Perficient: Drug Development

FEBRUARY 29, 2024

Eureka Server allows them to locate and get producer microservice instances as well as other information. So, other instances of the target may sit idle. To solve these problems, use the “ LoadBalancerClient ” type client component. return new ResponseEntity<String>("Final billAmount = billAmount - discount (RS.

Packaging 104

Packaging International 104

FDA Law Blog: Biosimilars

JULY 10, 2025

However, the vast majority of the CRLs posted in the openFDA database are already available in the action packages posted on FDA’s Drugs@FDA database and approved biologics product pages. 355(l) ) requires that action packages (which include CRLs, if issued) for approved original NDAs and BLAs (i.e.,

FDA 52

FDA Packaging Production Drugs 52

Drug Patent Watch

DECEMBER 12, 2024

This includes drug substance and drug product development, clinical trial logistics, product labeling, supply chain management, commercial packaging, and more. Best Practices for Evaluation Use Industry Benchmarks Utilize industry benchmarks to inform CDMO selection. How Industry Benchmarks Can Inform CDMO Selection.

Drug Development 93

Drug Development Production Pharmaceutical Companies Clinical Trials 93

Perficient: Drug Development

JULY 11, 2023

Every company needs documents for its processes, information, contracts, proposals, quotes, reports, non-disclosure agreements, service agreements, and for various other purposes. To get the document generation capabilities, you need to install ‘OmniStudio’ and ‘Salesforce Industry packages in the same org.

Packaging 81

Packaging Compliance Production Marketing 81

Agency IQ

JANUARY 19, 2024

Commission unveils “one substance, one assessment” reform package The Commission has long aspired to realize its one substance, one assessment concept in the EU’s chemical regulatory regime. Chemical information stemming from Union legislation will be included. The proposed regulation is divided into 9 chapters.

Packaging 40

Packaging Regulations Laboratories Animal Testing 40

FDA Law Blog: Biosimilars

JUNE 25, 2025

The requirement for the single-unit or unit-dose containers is not a substitute for special packaging, i.e., child resistant packaging required for certain products under the Poison Prevention Packaging Act and implementing regulations. See 16 C.F.R.

FDA 59

FDA Packaging Drugs Production 59

Perficient: Drug Development

MARCH 8, 2024

This managed package includes Apex classes and four key lightning components that are used to display Personalization data. This token exposes all datasets in Personalization and their information. Event Stream Component This component gives you information about the interactions your contact or lead is having with the site.

Packaging 110

Packaging Marketing Production Science 110

SCIENMAG: Medicine & Health

JULY 21, 2023

Katy Börner’s team from the Luddy School of Informatics, Computing, and Engineering’s Cyberinfrastructure for Network Science Center has made significant contributions to constructing a Human Reference Atlas and has led or co-authored six research articles in a just-released HuBMAP package in Nature. Börner, Victor H.

Research 66

Research Packaging Engineering Science 66