Broad Institute

JANUARY 14, 2025

His lab had just developed base editing, a gene-editing approach that makes single-letter changes in DNA and can shut down protein production using strategies including installing a stop signal in the genetic code. In 2018, Liu, who works on the same floor as Minikel and Vallabh at Broad, approached them and proposed a collaboration.

Disease 144

Disease DNA Protein Production Treatment 144

The Pharma Data

MAY 14, 2021

Product Name: Package | Prasara Yoga. Click here to get Package | Prasara Yoga at discounted price while it’s still available… All orders are protected by SSL encryption – the highest industry standard for online security from trusted vendors. You will NOT receive a physical package shipped to you in the mail.

Packaging 52

Packaging Production Doctors International 52

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.

Packaging 52

Packaging Production 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

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.

Production 82

Production Government Packaging Research 82

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.

Packaging 52

Packaging Production 52

Pharmaceutical Development Group

JULY 7, 2021

Introduction FDA (can also be expanded as the Food and Drug Administration) is a bureau that administers the public’s welfare by controlling and surveillance of food products, medications, vaccines, medical devices, etc. There are certain rules and criteria for post marketing safety reporting of FDA combination products.

Production 52

Production FDA Packaging Vaccine 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

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.

Compliance 59

Compliance Production Packaging Government 59

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.

Production 64

Production Compliance Regulations FDA 64

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)

Packaging 52

Packaging Production 52

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.

Virus 95

Virus Packaging Production 95

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.

Treatment 105

Treatment Packaging Clinical Research Therapies 105

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 […]

Packaging 87

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.

Packaging 87

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.

Packaging 98

Packaging Production 98

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.

Production 52

Production Efficacy & Potency Packaging Drugs 52

The Pharma Data

FEBRUARY 19, 2022

Food and Drug Administration is alerting the public that several categories of FDA-regulated products purchased from Jan. The FDA is working with the company to initiate a voluntary recall External Link Disclaimer of the affected products. Families rely on stores like Family Dollar for products such as food and medicine.

Production 52

Production FDA Packaging Regulations 52

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.

Drug Development 98

Drug Development Production Clinical Trials Pharmaceutical Companies 98

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.

Production 52

Production Therapies DNA Virus 52

Cytel

OCTOBER 23, 2023

The Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) are the two main divisions of the FDA responsible for regulating drugs and biological products, as well as combinations of drugs and biological products.

Packaging 69

Packaging Vaccine Regulations Production 69

biobide

NOVEMBER 20, 2023

The justification for this growth projection lies in the increased popularity and demand for skincare and personal care products, joined by the aging of global population. Such concerns have led to strict regulations regarding the formulation of cosmetic products.

Packaging 64

Packaging Regulations Production Marketing 64

PPD

MARCH 11, 2025

It involves addressing the specificity of research questions, the clinical and investigational product context, and underlying causal frameworks; selection of a suitable data source; and a deep understanding of RWD provenance, granularity, completeness, structure and curation.

Drug Development 52

Drug Development Clinical Trials Disease Trials 52

Perficient: Drug Development

OCTOBER 15, 2024

That’s the essence of Salesforce CPQ product bundles – taking individual products and services and transforming them into irresistible offerings for your customers. You’ve got your core product, add-on features, and maybe some implementation services. But what if you could package them neatly into tailored solutions?

Packaging 52

Packaging Production Marketing 52

Fierce BioTech

OCTOBER 8, 2024

Ana Kuschel Francis Carroll Sonia Adamidis Marc Uerdingen Duration 90 Minutes Join West experts to learn about solutions for today’s drug products and tomorrow’s novel applications and gain insights to understand and execute a risk-based critical thinking approach related to injectable drug packaging and delivery.

Packaging 52

Packaging Drugs Production 52

FDA Law Blog: Drug Discovery

DECEMBER 7, 2022

This product was developed by uniQure prior to being licensed to CSL Behring. We know, for example, the use of viral vectors results in antibody production that could inhibit future administration of gene therapies using the same or similar viruses, which will inform treatment decisions by patients with their doctors.

Therapies 119

Therapies FDA FDA Approval Treatment 119

Agency IQ

JULY 26, 2024

FDA finalizes guidance on electronic submissions for OTC products FDA has fulfilled its commitment under the Over-the-Counter Monograph Drug User Fee (OMUFA) program to issue final guidance on how sponsors can electronically submit monographs and other documents. These products are regulated differently from traditional prescription drugs.

FDA 40

FDA Production Packaging Regulations 40

Perficient: Drug Development

MAY 1, 2024

Just installing the packages and it’s enough for most cases. You don’t have export the production database every time you run the migration. Props You don’t have to create any logic or any API endpoints for the migration at the source application.

Packaging 105

Packaging Production 105

Perficient: Drug Development

JULY 11, 2023

To get the document generation capabilities, you need to install ‘OmniStudio’ and ‘Salesforce Industry packages in the same org. Within the package, you get the tools necessary to optimize the document generation process. A sample functionality comes with the package.

Packaging 81

Packaging Compliance Production Marketing 81

FDA Law Blog: Biosimilars

AUGUST 27, 2023

the ability to associate the saleable return product with the transaction information/statement with the particular product). the ability to associate the saleable return product with the transaction information/statement with the particular product). Drug manufacturers have had electronic systems in place since 2017.

FDA 52

FDA Packaging Production Drugs 52

FDA Law Blog: Biosimilars

JUNE 26, 2024

It includes questions about the product, that when answered, reveal additional information that should be supplied with a submission. package labeling is optional). In the “Description” section the applicant should describe any medical device functions of the product that would require a premarket submission.

FDA 98

FDA Regulations Production Packaging 98

Drug Target Review

AUGUST 6, 2024

Therapeutic areas with fewer competitors or novel targets can be attractive, offering companies the chance to establish leadership and differentiate their products. Manufacturing ADCs involves scaling up production while maintaining quality, navigating complex processes and implementing rigorous quality control measures.

Therapies 119

Therapies Pharmaceutical Companies Disease Treatment 119

Perficient: Drug Development

MARCH 8, 2024

This managed package includes Apex classes and four key lightning components that are used to display Personalization data. Affinity Graph Component The affinity component gives you a better perspective on how your contact or lead interacts with a client’s product.

Packaging 110

Packaging Production Marketing Science 110

PLOS: DNA Science

MARCH 14, 2024

Billions have been invested since 2016 in search of cultivated meat, but only a handful of products have emerged, in Singapore, the United States and Israel. If those challenges aren’t daunting enough, some efforts to cultivate meat have led to products that include mouse or rat cells. A $10,000 prototype isn’t encouraging.

DNA 98

DNA RNA Packaging Production 98

Agency IQ

NOVEMBER 10, 2023

The delayed enforcement is part of FDA’s finalized guidance, “Compliance Policy for Cosmetic Product Facility Registration and Cosmetic Product Listing.” MoCRA defines the term “ facility ” as the establishment of a manufacturer or importer that manufactures or processes cosmetic products distributed in the U.S.

Production 40

Production FDA Compliance Packaging 40

Fierce BioTech

JANUARY 3, 2025

This joint webinar presentation by West and Groninger, explores the unique challenges of Cell and Gene Therapies, mRNA LNP therapeutics particularly regarding cold storage requirements and their impact on packaging solutions. Click here to login. Listing Image WestPharma_ListingLogo_250x190.png On Demand Start Date Wed, 02/12/2025 - 11:00

Packaging 52

Packaging Therapies Pharmaceuticals Treatment 52

Fierce BioTech

JANUARY 3, 2025

This joint webinar presentation by West and Groninger, explores the unique challenges of Cell and Gene Therapies, mRNA LNP therapeutics particularly regarding cold storage requirements and their impact on packaging solutions. Click here to login. Listing Image WestPharma_ListingLogo_250x190.png On Demand Start Date Wed, 02/12/2025 - 11:00

Packaging 52

Packaging Therapies Pharmaceuticals Treatment 52