(CTPro™) Clinical Trials Management Professional Certification
At Biopharma Institute, we provide stellar learning programs via our online platform. Whether you are a business owner or a working professional, our online CTPro™ program will give you a competitive edge in the marketplace.
What is (CTPro™) Clinical Trials Management Professional Certification?
The (CTPro™) Clinical Trials Management Professional Certification program is offered by Biopharma Institute.
Also known as CTPro™, the Clinical Trials Management Professional Certification demonstrates that a student is proficient in understanding the responsibilities of all parties, from sponsors, to investigators and monitors. Good Clinical Practice requirements are described in detail, as well as regulatory guidelines for gaining approval for conducting clinical trails. The online CTPro™ program is perfect for individuals who don’t have the time to learn in a conventional classroom environment.
Who Should Get CTPro™ Certified?
If your job needs you to be involved in the clinical research, you are definitely suited to undertake these online courses. The curriculum of this CTPro™ certification is designed to give participants a practical and thorough understanding of all clinical research, the required processes for documentation, from both a procedural and regulatory perspective. If you want to gain comprehensive insight into areas such as the role that the Food and Drug Administration plays in your country, early clinical trial development processes, and requirements of trial reporting and monitoring of adverse events, it is highly recommended that you enroll in this online program.
Overview of CTPro™ Coursework Details
A typical CTPro™ program contains a long mix of foundational and advanced course modules. Below is a sneak peek of some of the coursework you might undertake:
- ICH-GCP Good Clinical Practice
- Clinical Trial Monitoring: Site Evaluation and Set-up
- Clinical Trial Monitoring: Documentation and Closure
- Clinical Trials and Drug Development
- Clinical Trials: Preparation and Design
- Clinical Trials: Preparing for an Audit or Inspection
- Application Process to Conduct FDA-regulated Clinical Trials in USA
- How to Obtain Approval to Conduct Clinical Trials in the EU
Benefits of Taking the CTPro™ program at Biopharma Institute
There are many upsides when you choose Biopharma Institute for your CTPro™ program preparation needs. Below are some reasons why:
- Highly qualified customer service team: Our customer service team is dedicated to helping you select an online training solution that not only fits your educational needs but your budget too.
- Course recognized by a broad range of industries: Our online courses give you the necessary knowledge and skills that can be called upon when needed. Our online classes are recognized by a great array of industries.
- Convenient and flexible course formats: Whether you choose to facilitate your learning before or after work, you will find that our online training formats are sufficiently flexible to accommodate both personal schedules and organizational concerns.
- Advanced eLearning tools: We employ the most advanced eLearning training techniques on the market. Since our inception, we have been assisting companies educate their employees. Coupled with new automated tracking systems, we ensure that the learning experience is second to none.
- We cater to training projects of any size: We have two decades of managing training projects of all sizes. Biopharma Institute has a consistent track record of assist professionals further their understanding of their industry and even uncover new discoveries.
Prepare for the CTPro™ program at Biopharma Institute Today!
To view our complete clinical training course catalog, click here.
If you are interested in participating in our online CTPro™ program courses, you can send us an email to support@biopharmainstitute.com or call us at (888) 424-6576.
