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GCP: The IND, How to Gain Approval for Clinical Trials in the USA (GCP007)

Certification Training Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
CPD Accredited TrainingAccreditation: This training course offers CPD accreditation from the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians.
CPD Credits: 3
Demonstration: Demo an online course.

Certificate: View sample certificate.

PRICE: USD $195.00 LogoTraining Program: GCP: The IND, How to Gain Approval for Clinical Trials in the USA
Training Provided By:

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

The IND (Investigational New Drug) Application is a submission through which the sponsor seeks approval from the FDA (Food And Drug Administration) to conduct clinical studies with an investigational drug. This online course will give students who are, or are becoming, regulatory professionals, the necessary detail and background required in order to complete and submit, for FDA approval, an IND application. An IND must contain various pieces of information covering areas such as clinical protocol, manufacturing, toxicology, drug distribution, and animal pharmacology. The application is a stepping stone that is crucial, from nonclinical all the way to clinical testing.

Once all course requirements have been satisfied, a Certificate of Completion is immediately available. Course takers can attempt the final assessment any number of times, as needed in order to achieve a passing grade.

Benefits of Getting Certified at

By employing advanced e-learning training techniques, and coupling them with new automated tracking systems, the provides professionally designed online courses which are effective at training, and assist those interested with advancing their careers. The also assists companies through maintaining training records, the education of their employees, and assisting them with improving their overall quality of service. The has assisted companies both abroad and throughout the United States for two decades. Through various learning tools our online courses offer proven methods that can help individuals and/or companies stay on top of the latest changes in the clinical research, pharmaceutical, and healthcare industries.

Have Questions?

Should you have any particular question about this course, you can call us at (888) 111-1111 or send us an email at for more information.

Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.

Online Training Programs Include:

  • Immediate access to training: Instructions, password, and username are emailed following order
  • 90 days of 24/7 access to individual training programs / 180 days for Professional Certification Program
  • Programs include voice-overs, easy navigation, progress checks, and high-quality animations
  • Course notes (in PDF) and/or references available with select training programs
  • Online final assessment with multiple-choice questions can be taken an unlimited number of times, until passing grade is achieved
  • A Certificate of Completion is immediately available once course requirements have been satisfied

The GCP: The IND, How to Gain Approval for Clinical Trials in the USA Course is Found in the Following Professional Certification Program(s):

Clinical Trials Management Professional Certification Program: This professional certification program is designed for clinical managers, project managers, and clinical research associates and coordinators, or those with desire to grow their career into these positions. Co … Learn more


Regulatory overview: This session briefly describes the legislative guidelines that apply to obtaining FDA approval to conduct clinical trials in the USA.

An introduction to Investigational New Drug Applications: This session provides a brief overview of the IND and of the submission process.

IND content and format requirements: Explore the specific format and content requirements of an IND application as specified by the Center for Drug Evaluation and Research (CDER).

The IND review and approval process: This session discusses the FDA review principles for IND applications, with a view to improving your application.

Maintenance of an IND: This session outlines the different types of IND amendments, when they are required, and the regulations that govern them.

Summary: Key point summary for all topics covered in This online course. Ideal for review, a refresher or a consolidation of learning points.


Students completing this course should be able to:

–Describe what an IND is, and why it is needed.

–Access the key regulatory documents surrounding INDs.

–Describe the content and format of an IND application.

–Describe the IND review and approval process.

–Describe the IND reporting requirements, and the types of amendments that can be made to an IND.


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