Perficient: Drug Development

FEBRUARY 19, 2024

Document-less servers, like Eureka Server, are known. The details appear as follows when we publish several instances of various microservices to an R&D server like Eureka Server. Diagram: – Eureka Server Internal Structure. To put it another way, the server does not contain any XML or JSON files.

Packaging 101

Packaging International 101

Perficient: Drug Development

AUGUST 14, 2023

Document all actions taken in Google Optimize. Documentation Checklist should include: A/B testing results Personalization campaigns Goals and Metrics setup Google Analytics audience setup Development workflows and troubleshooting documentation 2. Remember, the best tool for you depends on your specific needs and context.

Packaging 98

Packaging Marketing Trials Production 98

Perficient: Drug Development

JULY 19, 2023

Salesforce provides extensive documentation that lists the available metadata types and their specific XML names. Salesforce’s Metadata API documentation offers a comprehensive list of available component types to help you make the correct selections. Now, let’s discuss a code snippet and understand its contents: <?xml

Packaging 52

Packaging 52

Perficient: Drug Development

JUNE 25, 2024

To do this, utilize PDFBox, a Java library for managing PDF documents, in combination with Selenium, a potent web automation tool. It enables the creation, modification, and extraction of content from PDF files by developers. Key Features: PDF Creation: Enables the creation of new PDF documents from scratch.

Packaging 52

Packaging 52

Perficient: Drug Development

NOVEMBER 21, 2024

Step 1: Installing and Importing Dependencies for the Date Range Picker Component We will start by installing the required package. If you’re looking for more detailed documentation, you can check out the official vue2-daterange-picker documentation.

Packaging 105

Packaging International 105

DrugBank

SEPTEMBER 12, 2024

At DrugBank we’re committed to improving your daily research and drug development operations. Designed with your needs in mind, the DrugBank Data Dictionary addresses this challenge by providing comprehensive documentation for every table and column in our knowledgebase.

Production 78

Production Government Packaging Research 78

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 52

Packaging Production 52

The Premier Consulting Blog

APRIL 15, 2024

It is critical that the nonclinical program outlined in the PIND briefing document is presented in a manner that allows FDA to provide relevant input on the required IND-enabling studies. For example, if the nonclinical data presented in the PIND briefing document lacks information on the potential toxicity profile of the drug (e.g.,

FDA 52

FDA Pharmacokinetics Laboratories FDA Approval 52

Perficient: Drug Development

AUGUST 8, 2023

I have gone through multiple Sitecore documents and consolidated all the details in following steps. Install the Sitecore JavaScript Rendering SDK Forms for React package, along with its dependencies, in a JSS React or Next.js Sitecore does not have any out of the box (OOB) component to implement Sitecore Form. application.

Packaging 98

Packaging 98

Perficient: Drug Development

NOVEMBER 7, 2023

This platform facilitates AI developers in constructing applications that amalgamate Large Language Models, such as GPT-4, with external data sources and computational capabilities. The framework is equipped with both Python and JavaScript packages. How does langChain work? In the constants.py In the constants.py

Packaging 52

Packaging Engineering Research 52

Perficient: Drug Development

FEBRUARY 29, 2024

All the mutable scala collections will be under this package – scala.collection.mutable. Mutable Collections (from scala.collection.mutable package): Scala provides various other mutable collections like ArrayBuffer, HashMap, Queue, LinkedList, etc. Let’s explore some mutable data structures.

Packaging 52

Packaging 52

FDA Law Blog: Drug Discovery

DECEMBER 6, 2024

As much of the content of this draft guidance for cellular and gene therapy (CGT) products is articulated elsewhere, this document serves as a one-stop shop or Cliffs Notes for the numerous guidance documents now covering CGT product development. CBER will not commit to reviewing packages greater than 250 pages.

Therapies 59

Therapies FDA Production Disease 59

FDA Law Blog: Drug Discovery

SEPTEMBER 27, 2023

The meeting package for Type D meetings should be included with the meeting request. FDA intends to provide preliminary responses to Type D meeting packages no later than 5 calendar days before the meeting date. The goal for meeting minutes is the same as all other meeting types – 30 days after the meeting.

FDA 64

FDA Packaging Animal Testing Production 64

Perficient: Drug Development

DECEMBER 8, 2023

There was an issue that occurred after adding a package: the compiler errored out demanding to specify the exact version number of this package. I ended up with this config patch: <?xml xml version="1.0"?>

Packaging 78

Packaging International 78

Perficient: Drug Development

OCTOBER 30, 2023

I accidentally had my max depth set at 0 and only got one document. Document Extractors ( Part 4 ) As mentioned in this article, there are three types of document extractors. A document extractor can have multiple extractors. I’ll cover advanced document extractors in a future post. CSS, Xpath and JS.

Production 52

Production Packaging 52

Perficient: Drug Development

FEBRUARY 14, 2024

In the past, deploying UI updates has required packaging them alongside OSGi bundles and HTL-driven components. Furthermore, front-end developers and designers often need to only focus attention on the app experience. While this is still a usable way to deploy projects in AEM, it cannot isolate the UI and hot reload updates.

Packaging 52

Packaging Production 52

Advarra

JUNE 28, 2022

Failure to Have a Pre-Investigational New Drug (IND) Meeting. There are a myriad of regulations coming into play during the drug development process. Providing brief points to serve as a guiding point throughout the documents helps reviewers know what is relevant in the application.

FDA 52

FDA Regulations Clinical Trials Packaging 52

Codon

APRIL 9, 2024

However, the blandly clinical package of artemisinin and artesunate tablets reveals little about how the key compound was first discovered. “Cumulatively the deadliest of the human infectious diseases,” malaria has been documented throughout recorded history. It was from these texts that artemisinin was rediscovered.

Drugs 129

Drugs Science Research Doctors 129

Perficient: Drug Development

MARCH 19, 2024

The main driver behind the name change it seems is that Artifact Registry can manage more than just containers, such as OS and language packages. Google provides documentation and tooling to help the Container Registry to Artifact Registry migration. I first checked out a blog on this topic from Google.

Packaging 52

Packaging Production 52

Perficient: Drug Development

FEBRUARY 28, 2024

Immutable Collections (from scala.collection.immutable package): Scala provides various other immutable collections like Queue, Stack, LinkedList, etc. References: Here are the Spark documents delving further into the creation of immutable data structures in Scala.

Packaging 52

Packaging 52

Perficient: Drug Development

JANUARY 22, 2024

Optional.empty() is part of the java.util package and is primarily used in Java programming for working with the Optional class. For more details about the parameters, you can refer to the particular section in the documentation mentioned below.

Packaging 52

Packaging 52

Perficient: Drug Development

JUNE 24, 2024

CTA Action Button (Shopify landing page) Composable Commerce Principles: Modularity : The commerce platform is decomposed into individual packages or components, each responsible for specific functions such as product management, cart, payment processing, search etc. It requires significant development resources to implement.

Compliance 52

Compliance Packaging Marketing Production 52

Perficient: Drug Development

NOVEMBER 8, 2023

and npm (Node Package Manager) by running the following commands in your terminal. 5) node modules Directory: All the project’s dependencies and packages are stored in this directory, typically managed by package managers such as npm or Yarn. 9) README.md: Documentation for your project. version 10.6.0

Packaging 52

Packaging Production 52

Perficient: Drug Development

FEBRUARY 8, 2024

Even if they are not publishing documents and assets, portals will typically require managing content and translations for labels, alerts and help text, not to mention the need to integrate marketing messaging as part of the customer portal experience. But portals almost always have content management specific needs.

Marketing 52

Marketing Packaging 52

Agency IQ

FEBRUARY 12, 2024

As the FDA has previously acknowledged : “Many complex drug products did not exist” when the Hatch-Waxman Amendments were first passed into law. “As As drugs have increased in complexity in recent years, the scientific and regulatory roadmaps for drug development and approval may not be as well-established for more complex generics.”

FDA 40

FDA Packaging Production International 40

Perficient: Drug Development

SEPTEMBER 11, 2024

As Lit’s documentation says, the advantage of this approach is that, since modern components rely on standard HTML and JavaScript APIs, they are supported by almost all web browsers (all web browser that support the required HTML and JavaScript APIs, that is), and do not require any frameworks such as Angular or React to run.

Packaging 52

Packaging 52

Perficient: Drug Development

FEBRUARY 8, 2024

Both platforms offer extensive documentation and features to explore. Step 2: Creating Your Streamlit App Create a Python file : Start by creating a new Python file for your project (e.g., With Streamlit and OpenAI, you can transform your ideas into interactive AI web apps with ease. Moreover, remember, this is just the beginning.

Packaging 52

Packaging Science 52

Perficient: Drug Development

DECEMBER 18, 2023

For precise and up-to-date information on these dependency versions, it is highly recommended to refer the IBM documentation. Recommended IDE: You can use any IDE or development tools of your choice. packages/apps/store-root-app packages/libs/common-components Applications defined in core-import-map.json.

Packaging 52

Packaging Production 52

Perficient: Drug Development

MAY 8, 2024

Document Metadata. This compiler will handle re-rendering internally, eliminating the need for developers to explicitly implement useMemo , memo , and useCallback. Document Metadata In the past, adding metadata such as titles and meta descriptions to React applications was a cumbersome process.

Packaging 52

Packaging International 52

Perficient: Drug Development

FEBRUARY 15, 2024

Most of them needs to be imported from spark packages. Dataset: There are many DataFrame methods which are subclassified into Transformation and Action based upon the operation performed, you can learn more about these in this blog – Spark RDD Operations (perficient.com). Let’s see some of the basic and regularly used ones.

Packaging 52

Packaging 52

The Premier Consulting Blog

NOVEMBER 4, 2023

More importantly, the development of scientifically justified analytical methods and in-process controls can demonstrate impurity control sufficient for IND opening. The impact of the device on the drug product quality attributes and safety are suitable issues for discussion in the pre-IND meeting. Contact us to learn more today!

Clinical Pharmacology 52

Clinical Pharmacology Production FDA Packaging 52

Perficient: Drug Development

MAY 3, 2024

[CDATA[Adobe Experience Manager (AEM) Assets is a digital asset management system (DAM) that is built into AEM. adaptTo(ValueMap.class); title = StringEscapeUtils.escapeXml(null ! rss.xml"; linkTag = RssFeedUtils.setLinkElements(link); ValueMap properties = resource.getChild(JcrConstants.JCR_CONTENT).adaptTo(ValueMap.class);

Packaging 52

Packaging 52

Agency IQ

JULY 22, 2024

AgencyIQ compiles these data using information in approval letters, labeling and review packages posted to the Drugs@FDA database. In this document, the agency describes how to design a DAP, which should set enrollment goals using data about the incidence and/or prevalence of a disease in the U.S. population.

Clinical Trials 52

Clinical Trials Trials Science FDA 52

Agency IQ

MAY 17, 2024

How have pre-submission meetings for generic drug applicants changed under GDUFA III? Under GDUFA III, the scope and purpose of pre-submission meetings for generic drug developers has changed. The generic drug user fee program is currently on its third iteration (i.e., What to expect on the day of the meeting?

Science 40

Science FDA Drugs Production 40

Perficient: Drug Development

JANUARY 16, 2024

There is, of course, documentation out there from Sitecore as well as a ton of excellent content from the many helpful experts in the Sitecore community on these two SaaS products from Sitecore. I won’t be going into great detail on Experience Edge or XM Cloud as products in this post. This worked fine for a while.

Packaging 52

Packaging Engineering Production 52

Perficient: Drug Development

NOVEMBER 30, 2023

For example, my local development Sitecore 10.3 but the latest NuGet package is version 6.2 Sitecore documentation recommends using /sitecore and /sitecore/admin URLs to access Sitecore. It is a good thing to have everything documented in one place. instance is referencing IdentityModel.dll version 3.10.10

Packaging 52

Packaging 52

Agency IQ

MAY 3, 2024

FDA’s Diversity Action Plan guidance: The FDA’s hotly-anticipated revised draft guidance document is currently under review at the White House’s Office of Information and Regulatory Affairs (OIRA), and we anticipate that it will be published over the next two months.

FDA 40

FDA Science Regulations Clinical Trials 40