Search
Search
Search
Close this search box.

Optimizing Preclinical Study Timelines with Master Schedule Management

Effective master schedule management can keep a preclinical timeline on schedule. Learn more when you read our blog today.

Blog Master Schedule Management and Its Importance to Preclinical Study Timelines Preclinical studies are the process of cells or animals before they make their way to human trials. This process is vital to the development process as it’s used to see which drugs are safe to continue testing. Optimizing the process can help speed up […]

How to Accelerate Drug Discovery and Development Time to Market

Blog Accelerating the Drug Discovery and Development Process with Xybion’s Pristima XD Drug discovery and development is a crucial and complex process in the pharmaceutical industry. Its goal is to get new drugs to market as quickly and efficiently as possible. However, this process involves many steps and can be time-consuming, especially in the preclinical […]

Major Considerations While Doing Preclinical Studies

Blog Navigating Preclinical Studies: Key Considerations to Keep in Mind Are you looking to navigate preclinical studies for your laboratory? It’s crucial to understand the key considerations required to ensure your preclinical study’s success. Good laboratory practices (GLP) are essential during the preclinical stage, with eight subparts. Navigating preclinical studies may seem overwhelming, but with […]

Choosing the Best Preclinical Software for Your Company: A Complete Guide

Blog Choosing the Best Preclinical Software Did you know that the drug discovery industry is projected to exceed $150 billion in value by 2030? In order to thrive in this market, you will need to make use of preclinical software to help achieve your target metrics. Not everybody understands what to look for when searching […]

Reducing Your Preclinical Regulatory Burden Through a Unified Solution

Blog Challenges in Drug Discovery Studies show the average cost of bringing a new drug to market is close to $1 trillion. Healthcare firms face a considerable regulatory environment and administrative burden. Professionals in the field note these items as key challenges to delivering effective products. Organizations must comply with an ever-increasing and wide-ranging body […]