The Pharma Data

JULY 2, 2025

High viscosity , aggregation risks , and stability issues often complicate both upstream and downstream processes, including manufacturing, packaging, and storage. Despite these benefits, the development and commercialization of high-concentration biologics come with formidable challenges. WuXiHigh™ 2.0:

FDA Approval

PPD

NOVEMBER 11, 2024

As companies undertake these steps, they increasingly rely on supply partners like Thermo Fisher who can address challenges in real time, helping maintain the highest levels of quality throughout the process without losing time or momentum.

Drug Development

The Pharma Data

JUNE 18, 2025

Unparalleled Access to Merck’s Biotech Ecosystem As part of its award package, Neoclease will receive broad support from Merck’s network of scientific resources.

Therapies

Broad Institute

JANUARY 14, 2025

Building on previous work by the vector-engineering lab of Ben Deverman at the Broad, the team developed a pair of adeno-associated viruses (AAVs) to package and deliver the base-editing machinery to brain cells. But the researchers needed to deliver the base editors to the brain.

Disease

Perficient: Drug Development

DECEMBER 30, 2024

Continuous Deployment (CD) takes validated code packages from the build process and deploys them into a staging or production environment. Developers can track successful deployments and narrow issues to specific package versions. Connect to App Catalog We need to authenticate against our tenant’s app catalog.

Packaging

Broad Institute

JUNE 24, 2025

It also needed to be delivered directly to the liver cells in his body, rather than to cells in a lab, and this was achieved by packaging the base editor in a lipid nanoparticle, a delivery system conceptually similar to the one used to deliver COVID vaccines to billions of people. He needed a personalized, one-of-a-kind therapy.

Treatment

Drug Target Review

MAY 14, 2025

The opportunity lies in packaging AI into controlled environments where we understand inputs, possible outputs, and have monitoring systems. However, when applied to customer interactions that directly impact financial gain or loss, especially with fiduciary responsibilities involved, trust becomes far more complicated.

Drugs

Perficient: Drug Development

FEBRUARY 27, 2025

Any content that needs to be updated in production environments should be packaged to a lower environment, using Groovy Console to update and validate content. return template } After creating a package using Groovy script on your local machine, you can directly install it through the Package Manager.

Packaging

PPD

MARCH 11, 2025

Addressing evidence gaps early enables health technology developers to optimize their development strategies and plan their health economic modelling sooner, to provide robust and comprehensive evidence packages that support their product’s value proposition.

Drug Development

The Pharma Data

JUNE 24, 2025

securing a funding package of up to $2 billion. With a total package of up to $2 billion, the agreement between Royalty Pharma and Revolution Medicines underscores growing investor confidence in the viability and future of targeted RAS inhibition.

Clinical Development

The Pharma Data

JUNE 25, 2025

By moving to tablets, BeOne estimates a reduction in bottle size by approximately 70%, which not only decreases plastic use but also facilitates more efficient packaging and transportation. This initiative is part of the company’s broader sustainability efforts aimed at reducing its environmental impact and improving supply chain efficiency.

Packaging

Broad Institute

MAY 27, 2025

To shuttle the base editors to specific cells in mice, the researchers packaged them into dual AAV9 vectors, an adeno-associated virus designed to deliver cargo to neurons. The base editors stabilized the repeat tracts in mouse models of Friedreichs ataxia and Huntingtons disease.

DNA

Predictive Oncology

JUNE 5, 2025

This information can improve the probability of technical success and strengthen the data package for the commercialization of submitted compounds. The POAI platform provides data (wet lab and active ML modeling) back to researchers based on access to an otherwise unreachable number of primary patient responses to their drug candidates.

Packaging

Fierce BioTech

JUNE 12, 2025

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Disease

Drug Target Review

JUNE 2, 2025

Each stage must adhere to strict quality and regulatory standards, even before considering fill-finish and packaging. This includes antibody production (often using mammalian or microbial platforms), linker-payload synthesis, and the bioconjugation process itself.

Small Molecule

Perficient: Drug Development

FEBRUARY 26, 2025

Run SqlPackage Put.bacpac file into the package folder.(ex: Install the Tool Follow the instructions under the “Windows (.NET NET 6)” header to download and extract the tool. After extracting, open a terminal in the directory where you extracted SqlPackage. ex: C:sqlpackage-win7-x64-en-162.1.167.1)

Packaging

The Premier Consulting Blog

DECEMBER 10, 2024

Validation involves detailed documentation of every step of the production process, from raw material sourcing to final product packaging in good manufacturing practice (GMP) compliant facilities. The objective is to demonstrate that the manufacturing process consistently produces a product that meets all predefined specifications.

Marketing

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

Pharma Manufacturing

JULY 24, 2025

Marc Casper says the Ridgefield site, which specializes in fill‑finish and packaging of aseptic injectable medications, aligns with its plans to bolster U.S. capacity.

Packaging

New Drug Approvals

JULY 25, 2025

“Drug Approval Package: Agamree” U.S. Archived from the original on 18 February 2024. Retrieved 14 March 2024. This article incorporates text from this source, which is in the public domain. Food and Drug Administration (FDA). 7 November 2023. Archived from the original on 13 November 2023. Retrieved 13 November 2023.

FDA

Codon

JANUARY 5, 2025

A package containing 100 cc. The soldiers stuffed their pockets with the small packages of albumin and administered it to many seriously wounded men, most of whom lived to be evacuated to ships and receive further medical care. On the third morning the edema had disappeared and the patient was able to eat breakfast.

Laboratories

Chemical Biology and Drug Design

DECEMBER 5, 2024

The differentially expressed genes (DEGs) of PC were obtained with the limma package in R. In this work, three PC-related microarray datasets (GSE183795, GSE28735, and GSE62452) were analyzed. Weighted gene co-expression network analysis (WGCNA) and machine learning approaches were used to screen the hub genes.

Packaging

Drug Patent Watch

JANUARY 9, 2025

Take the time to clearly define your technical needs, from drug substance manufacturing to packaging requirements. Assessing Your Technical Needs Every drug is unique, and so are its manufacturing requirements.

Compliance

The Pharma Data

JUNE 13, 2025

This favorable opinion, following a rigorous evaluation by European regulators, is based on a comprehensive package of data demonstrating the medication’s quality, safety, and efficacy. Importantly, the CVMP recognized that the benefits of Zenrelia decisively outweigh any potential risks for dogs with these conditions.

Treatment

Pharma Manufacturing

JULY 21, 2025

When not covering the pharma manufacturing industry, he is an avid Buffalo Bills football fan, likes to kayak and plays guitar.

Therapies

The Open Targets Blog

JANUARY 30, 2025

gget ( [link] ) is a free, open-source command-line tool and Python package designed to enable efficient querying of large genomic databases, such as Ensembl, UniProt, and NCBI. We chatted to the team about the module, and how it facilitates access to Open Targets Platform data. What is gget?

Bioinformatics

Codon

NOVEMBER 1, 2024

They engineered genetically-encoded RNA exporters, based on viruses, that package and secrete RNA molecules in protective nanoparticles, allowing non-destructive monitoring of those RNA molecules in real-time.

DNA

Perficient: Drug Development

JANUARY 30, 2025

You want a package manager to manage dependencies between Kubernetes. When to Use Helm and KubeOne Tool? Use Helm if: You want to manage and deploy applications on the Kubernetes cluster. You need an easy way to upgrade and roll back applications. Use KubeOne if: You are setting up, scaling, or managing Kubernetes clusters.

Packaging

BioPharma Drive: Drug Pricing

JUNE 24, 2025

Most Popular A longer ‘winter’: Public funding slowdown heightens pressure on biotech startups Novo abruptly ends obesity drug deal with Hims Compass’ big psychedelic study doesn’t impress investors Cidara stock soars as antiviral drug succeeds in flu study Library resources Survey Report Pharma's AI and RWD Revolution: Breaking Barriers to Growth (..)

RNA

FDA Law Blog: Biosimilars

MAY 4, 2025

DEA seized five packages in Eagle Pass, Texas, identifying IMC Pro as the shipper containing 26.4 IMC Pro did not store or handle the packages nor maintain records about their contents. of 1-BOC-Piperidone and 138.66 of (2-Bromethyl) benzene. Both chemicals are used in the illicit manufacturer of fentanyl.

Packaging

BioPharma Drive: Drug Pricing

JULY 14, 2025

PCI helps biopharmaceutical companies manufacture and package drug products used in clinical trials as well as commercially. That funding was supported by a “significant reinvestment” from current backer Mubadala Investment Co. and reportedly values PCI at $10 billion, according to The Wall Street Journal.

Production

Perficient: Drug Development

DECEMBER 19, 2024

By leveraging tools like pytest-html , allure-pytest , or pytest-splunk , you can generate rich and actionable test reports that greatly enhance the debugging process and provide clear feedback. Setting Up Pytest for Selenium Before we dive into reporting, let’s briefly set up Selenium with Pytest for a basic test case.

Packaging

Perficient: Drug Development

APRIL 7, 2025

Prepare your SFMC environment , ensuring that your Business Unit is properly configured and that administrative settings (including the Sender Authentication Package) are in place. Map out the migration timeline , accounting for potential downtime or overlapping platform usage.

Marketing

Perficient: Drug Development

DECEMBER 9, 2024

requirements.txt is a text file that lists the external libraries and packages your Python project depends on. This helps maintain a current and accurate list of required packages. What is requirements.txt? How to Create and Use requirements.txt for Testing 1.

Packaging

Perficient: Drug Development

APRIL 10, 2025

Package Name: Your preferred package name (e.g., Ensure your Android app (using the base package name like com.yourcompany.advancedconceptsapp ) is registered. package com.yourcompany.advancedconceptsapp.ui package com.yourcompany.advancedconceptsapp.ui // Imports: androidx.compose.*, Language: Kotlin. padding(16.dp).fillMaxSize())

Packaging

FDA Law Blog: Drug Discovery

DECEMBER 6, 2024

The draft guidance recommends that no more than 15 questions are included in the briefing package. CBER will not commit to reviewing packages greater than 250 pages. The draft guidance states that a pre-BLA meeting request should be submitted at least 4 months before the anticipated BLA submission.

Therapies

Drug Patent Watch

FEBRUARY 19, 2025

In the context of generic drugs, QA involves a range of activities, including: Conducting regular audits and inspections of manufacturing facilities to ensure compliance with regulatory requirements Testing finished products for purity, potency, and stability Verifying the accuracy of labeling and packaging Monitoring the supply chain to prevent contamination (..)

Drugs