Drugs.com

APRIL 4, 2025

FRIDAY, April 4, 2025 -- Common chemicals used in plastic and personal care products may interfere with brain development in babies, a new study says.Phthalates are found in many everyday items, like food packaging, shampoo, toys and vinyl.

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DrugBank

SEPTEMBER 12, 2024

The Complete Support Package While the Data Dictionary is your go-to resource for detailed field-level information, it works best in conjunction with our existing Help Centre , which provides broader context and guidance on using DrugBank data.

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Production Government Packaging Research 98

Perficient: Drug Development

FEBRUARY 27, 2025

Important things to know about Groovy Console Security Due to security concerns, Groovy Console should not be installed in any production environment. 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.

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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.

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Perficient: Drug Development

JUNE 2, 2025

package which added the following dependencies. Following channels were created: staging, uat, and production. Test: Unlike App center, Expo provides the same package for iOS and Android targets. The targeted version package is available on the expo server. It is caused by the react-native-elements package.

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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.

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Packaging Laboratories Pharmaceutical Companies Compliance 52

Fierce BioTech

JUNE 12, 2025

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Disease Packaging Compliance Drugs 52

Perficient: Drug Development

AUGUST 22, 2023

In this episode, we will continue exploring Sitecore Content Serialization and learn multiple options required for serialization along with the item packaging and deployment. But for the production release, we need to create a Sitecore Content Serialization package and configure it in the pipeline for continuous integration.

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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.

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Drug Patent Watch

MARCH 12, 2025

Behind the scenes, generic drug manufacturers are working tirelessly to ensure that their products are safe, effective, and identical to their branded counterparts. It helps them to identify potential issues early on, make adjustments as needed, and ultimately bring a high-quality product to market.

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Drug Patent Watch

FEBRUARY 19, 2025

From inspecting manufacturing facilities to testing finished products, QA teams work tirelessly to guarantee that every pill, tablet, or capsule that reaches the market is safe and effective. These dedicated individuals play a critical role in ensuring that generic drugs meet the same high standards as their brand-name counterparts.

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FDA Law Blog: Biosimilars

JULY 22, 2024

The American Conference Institute (“ACI”) is holding its 2nd West Coast Editionof its Legal, Regulatory, and Compliance Forum on Cosmetics & Personal Care Products from September 25-26 at the Le Meridien Delfina, Santa Monica, California. s John W.M. s John W.M. s John W.M.

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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: WuXiHigh™ 2.0: Source link

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FDA Law Blog: Biosimilars

MARCH 21, 2024

As the new law unfolds—and as state laws regarding ingredients and packaging, as well as laws regarding environmental claims continue to affect the cosmetics and personal care industries—the topics covered at the conference have never been more relevant. By John W.M.

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Production Compliance Regulations FDA 64

addgene Blog

JULY 25, 2023

For safety and production reasons, multiple plasmids with many components are used to package lab grown viruses. It can be intimidating at first to look at so many plasmid maps and protocols! In reality, there are many shared components across viruses (AAV, lentivirus, etc.) and their functions are more intuitive than you might think.

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Perficient: Drug Development

FEBRUARY 26, 2025

However, during the development cycle, there are occasions when having access to a local database environment becomes crucial, particularly for analyzing and troubleshooting issues originating in the production environment. Run SqlPackage Put.bacpac file into the package folder.(ex: ex: C:sqlpackage-win7-x64-en-162.1.167.1)

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Drug Target Review

JUNE 9, 2023

This research has resulted in the first TCR-based therapeutic product candidate from the partnership to advance into clinical development. Looking ahead, Genentech has responsibility for clinical, regulatory and commercialisation efforts for any T-cell therapy product candidate.

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The Pharma Data

JUNE 25, 2025

The company announced that the Committee for Medicinal Products for Human Use (CHMP), the scientific advisory body of the European Medicines Agency (EMA), has issued a positive opinion recommending approval of a new tablet formulation of BRUKINSA for all currently approved indications. Alignment with U.S.

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Packaging Pharmacokinetics Therapies Marketing 52

The Premier Consulting Blog

DECEMBER 10, 2024

The influence of CMC on the NDA process Identification of a promising molecule is just the start of a long journey to product approval. CMC is a critical component in the development strategy for an asset, and the FDAs expectations regarding a sponsors level of CMC product and process knowledge increases as a molecule advances to market.

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Perficient: Drug Development

DECEMBER 9, 2024

requirements.txt is a text file that lists the external libraries and packages your Python project depends on. Use Separate Files for Different Environments : If your project has different dependencies for testing, development, and production, consider creating separate requirements files (e.g., What is requirements.txt?

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Packaging Production 52

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 agreed to provide the Chinese companies with access to the shipping companys accounts for common carriers to generate domestic shipping labels for goods and products the Chinese companies sold or manufactured.

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SCIENMAG: Medicine & Health

SEPTEMBER 1, 2023

We are constantly exposed to phthalates in our environment through plastic products such as storage containers, medical devices, packages, fabrics, and toys. Specifically, di-isononyl phthalate is inevitably becoming a part of our lives. In a new study, researchers used mice […]

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Packaging Production Research 87

SCIENMAG: Medicine & Health

JULY 17, 2023

Indiscriminate use of packaging materials derived from petroleum has led to a huge buildup of plastic in landfills and the ocean, as these materials have low degradability and are not significantly recycled.

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Packaging Research Production 87

Perficient: Drug Development

OCTOBER 9, 2024

Optimizely Graph lets you fetch content and sync data from other Optimizely products. Install the following packages: StrawberryShake.Server StrawberryShake.Transport.Http. For content search, this lets you create custom search tools that transform user input into a GraphQL query and then process the results into a search results page.

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The Premier Consulting Blog

NOVEMBER 8, 2022

With the promise of simplified and improved treatments, the $118 billion combination-product market is projected to increase at a compound annual growth rate (CAGR) of 8.8%. e) reveals more detail — and gray areas: Two or more regulated components, in one package (e.g., The drug product is packaged and shipped as a solid powder.

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Production Efficacy & Potency Packaging Drugs 52

Perficient: Drug Development

MARCH 20, 2025

Unfortunately, this slows us down and hampers our productivity by introducing errors into the workflow. 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.

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FDA Law Blog: Biosimilars

JUNE 25, 2025

To be clear, the minor changes are permitted only for OTC monograph drug products that are included in deemed final orders, and not for OTC monograph products that may remain on the market pending FDA monograph orders allowing or prohibiting such products.) See 16 C.F.R.

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FDA Packaging Drugs Production 59

Drug Target Review

MAY 14, 2025

This isnt about hype or grand promises its about identifying low-hanging fruit and achievable productivity gains. Recently, we’ve been pursuing AI product initiatives that have made me consider why people might be resistant to AI tools, what AI tools are capable of in drug discovery, and their limitations.

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Drugs Science Government Production 69

The Premier Consulting Blog

MARCH 7, 2024

The analytical package, consisting of release, stability, and characterization tests, includes data generated throughout the product development and manufacturing process. For gene therapy vectors, this testing encompasses production cell lines, master and working cell banks (MCB, WCB), and virus banks.

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Perficient: Drug Development

APRIL 17, 2025

Equitable Use means designing products and services that are accessible to all users in the same way, without segregating or stigmatizing certain groups. Whether its in physical spaces, digital interfaces, or everyday products, everyone deserves the ability to interact without barriers. Heres why Equitable Use is vital for everyone.

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Packaging Pharmacy Compliance Production 52

Perficient: Drug Development

MAY 20, 2025

NLP provides significant search relevancy enhancements and includes modern and regularly updated packages. Range Filter The range filter feature allows the user to find products based on a price range filter. and dimensions (Length, Width, and Height) when searching for product quantities or measurement values.

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FDA Law Blog: Drug Discovery

DECEMBER 6, 2024

Valentine On November 19, 2024, FDA released a draft guidance titled Frequently Asked Questions Developing Potential Cellular and Gene Therapy Products. The draft guidance states that only one 90-minute pre-BLA meeting will typically be granted for a specific product or indication planned for an original marketing application.

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Drug Patent Watch

DECEMBER 12, 2024

Evaluating CDMO performance is a critical step in this process, ensuring that the chosen partner can meet the required standards and deliver high-quality products. This includes drug substance and drug product development, clinical trial logistics, product labeling, supply chain management, commercial packaging, and more.

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Drug Target Review

JUNE 6, 2025

Most are concentrating on the delivery van and not necessarily on the package,” he adds, highlighting the industry’s tendency to focus on antibody engineering while underinvesting in payload innovation. And we think the package is probably equally, if not more, important.” “It’s almost both worlds coming together”.

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Common Sense for Drug Policy Blog

OCTOBER 29, 2024

Limited Evidence for Nalfmefene "In 2021, due to the widespread availability of high-potency synthetic opioids like fentanyl, the US FDA approved two high-dose naloxone products, an 8 mg IN spray (Kloxxado) and a 5 mg IM injectable (Zimhi). mg IM vs. 8 mg IN and 2 mg IM vs. 5 mg IM, respectively).

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FDA Approval Pharmacokinetics Packaging FDA 52

SCIENMAG: Medicine & Health

JULY 27, 2023

Supported by the EU-call Circular Bio-based Europe Joint Undertaking (CBE JU), the research project establishes a value chain for sustainable products such as textiles, food packaging and reinforced composites ready for the consumer […]

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Packaging Production Research 74

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.

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