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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.

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 development time so that life-saving drugs can make their way to people quickly.

In this blog post, we’ll look at the challenges of preclinical study timelines. Additionally, we’ll dive deeper into what master schedule management is, along with how it can help prevent delays during the preclinical study timeline.

Want to learn more about master schedule management? Read on for everything you need to know.

The Challenges of Preclinical Study Timelines

When it comes to new drug development, clinical studies are what every team is pushing towards. However, preclinical studies are there to ensure that clinical studies are safe.

There are a few common challenges that arise within preclinical studies. These challenges can affect the study timeline and push back new drugs even further.

Common Reasons for Delays

There are several reasons that preclinical studies are delayed. While some of these reasons are related to funding, others are related to the complex nature of managing these studies.

Since so many regulatory obligations exist, dozens of tests need to be conducted. It is all in the hopes of meeting regulatory standards.

Consequences of Delays in Preclinical Studies

When preclinical studies get delayed, the drug will take longer to move to clinical trials. This delay rolls over and causes the new drug to take longer to get into the hands of those that need it.

Master Schedule Management in Preclinical Studies

Master schedule management is a great way to organize and focus your teams on the organizational goals of your lab. Here’s what you need to know about master scheduling and its role in preclinical studies.

What is Master Schedule Management?

Master schedule management is the process of planning and scheduling various tasks within a project. This is a key part of project planning as it takes all objectives and links them to a schedule.

This schedule can help outline the daily, weekly, and monthly goals for everyone working on the project.

Benefits of Using Master Schedule Management in Preclinical Studies

As mentioned above, preclinical studies are critical to ensuring that new drugs are safe for human trials. The preclinical process is designed to run tests and extract data efficiently. This data can then be used to determine if the drug is safe to move on.

It’s important to note that preclinical tests are not just one or two tests. In some cases, hundreds of tests may occur to determine if a particular compound is safe to proceed. It is where master schedule management comes in.

Master schedule management is a great way to organize, plan, and schedule all these tests. This schedule can also include each test’s objectives, deliverables, and  other relevant information.

In this way, master schedule management is the central planning tool for the entire study.

Components of a Master Schedule

Various components make up a master schedule. Here’s a quick breakdown of what you can expect.

  1. Project Objectives

The master schedule should be based on the project. It means that at a fundamental level, the plan should outline the objectives of that project.

  1. Work Breakdown Structure

The work that must be done within that project is also broken down. It helps clear the objectives and sets a path toward each goal.

  1. Tasks List

Work is always broken down efficiently as tasks. It enables task list to be shared and worked on by teams and team members.

  1. Task Sequencing

Once all tasks are noted, they can be sequenced to follow a logical path. It helps guide teams and team members toward organizational goals.

  1. Assigning Resources

Lastly, a master schedule can be used to allocate and assign resources. Since every task is outlined and planned, it’s easy to set resources centrally.

Key Considerations in Master Schedule Management

A few key considerations need to be made when creating a master schedule. The first of these considerations is to set realistic goals. Realistic goals are the best way to ensure that your entire team is focused on moving the project forward incrementally.

The next consideration is collaborating with stakeholders. Integrating this into your master schedule will keep all parties updated and in the loop for every new development.

Another important consideration is compliance. Your schedule should always consider this to ensure that your entire project abides by the latest regulations.

The Importance of Master Schedule Management

Master schedule management is essential to help plan and schedule your entire preclinical study. This can be done from day one to track every task assigned to the study. How much must be produced over a specific period is specified in your master schedule. If your master production scheduling is done correctly, it will be the foundation of a manufacturing company that will enable you adjust to changes in demand and stop stock shortages.

How Pristima XD Can Help with Master Schedule Management?

Implementing master schedule management is crucial for optimizing preclinical studies. By investing in effective management solutions, valuable admin time can be saved, leading to increased efficiency in the research process. Moreover, there are innovative solutions specifically designed to cater to the unique requirements of the medical, pharmaceutical, and research fields. Pristima XD is the perfect example of an all-in-one lab solution. As an integrated digital laboratory execution system, you can automate tasks and collect data throughout the preclinical process.

Unlock the potential of master schedule management and Pristima XD. Take the next step toward optimizing your preclinical study timelines. Book a demo now and witness the transformative capabilities of this state-of-the-art solution.

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