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Healthcare

Clinical Trials & Regulatory Affairs

Get the training to conduct clinical trials and fulfill the educational requirements to become a CRA or CRC.

Join the thriving clinical trials market
Conducting clinical trials is essential to ensure the safety and efficacy of new drugs, biologics and medical devices. The demand for highly trained professionals to coordinate and manage clinical trials for the local, national and international biomedical and biotech communities continues to grow rapidly. By learning key concepts, guidelines, regulations and best practices, professionals gain the skills needed to become part of an active workforce and fulfill the requirements to become a CRA or CRC through ACRP, or CRP through SoCRA.

Clinical Trials & Regulatory Affairs Programs & Certificates

Classroom type:
Live Online
In-Person
Online
Hybrid

Biotechnology Project Management

Explore the key skills needed for project management within the biotech environment from a clinical, technical and regulatory perspective.

Duration
9 months
Cost
$5,990

Clinical Trials Administration

This program is built on responsiveness to the changing demands of the new clinical trials economy, personal attention, and sound principles.

Duration
12 months
Cost
$2,835

Clinical Trials Design and Management

By learning key concepts, guidelines, regulations, and best practices, participants gain the skills needed to become part of an active clinical...

Duration
6 - 24 months
Cost
$5,100 - $5,700

Quality Assurance and Control

This program is designed for chemists, bio-chemists or biologists in the pharmaceutical and biologic industry who are new to quality assurance and...

Duration
12-18 months
Cost
$3,720

Regulatory Affairs Essentials

An excellent career for professionals who wish to work in a challenging and dynamic field that is at the center of science, business, government...

Duration
9 -15 Months
Cost
$3,345

Regulatory Affairs for Medical Devices

Provides professionals with the knowledge to work in this highly regulated environment and the process needed to develop medical devices from...

Duration
9 -15 Months
Cost
$3,820

Clinical Trials & Regulatory Affairs Courses

Classroom type:
Live Online
In-Person
Online
Hybrid
FPM-40685

CT: Documents in Drug Development: Writing Protocols, Reports, Summaries, Submissions, and Disclosures

Units
3.00
Cost
$645.00
FPM-40173

CT: Drug Development Process

Units
3.00
Cost
$645.00
FPM-40338

CT: Financial Management of Clinical Trials

Units
1.00
Cost
$325.00
FPM-40204

CT: Good Clinical Practices

Units
3.00
Cost
$645.00
FPM-40388

CT: Human Subjects Protection and IRBs

Units
2.00
Cost
$525.00
FPM-40494

CT: Monitoring Oncology Trials

Units
3.00
Cost
$645.00
FPM-40187

CT: Nuts and Bolts of Monitoring Clinical Trials

Units
2.00
Cost
$525.00
FPM-40233

CT: Practical Clinical Statistics for the Non-Statistician

Units
2.00
Cost
$525.00
FPM-40656

CT: Project Management in Clinical Trials

Units
3.00
Cost
$645.00
FPM-40207

CT: Prospective Preparation for Internal and External Audits

Units
1.00
Cost
$325.00
FPM-40189

CT: Regulation of Drugs, Biologics, Devices, and Diagnostics

Units
3.00
Cost
$645.00
FPM-40208

CT: Site and Investigator Recruitment

Units
1.00
Cost
$325.00
FPM-40493

CT: Understanding Oncology

Units
3.00
Cost
$645.00
FPM-40228

CT: Working with Clinical Research Organizations (CROs)

Units
1.00
Cost
$325.00
BIOL-40201

Good Documentation Practices

Units
3.00
Cost
$745.00
BIOL-40244

In Vitro Diagnostics Product Development

Units
2.00
Cost
$625.00
BIOL-40322

Overview of Regulatory Affairs for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40323

Quality Management Systems for Medical Devices

Units
3.00
Cost
$745.00
BIOL-40101

Regulatory Compliance for Drugs & Biologics

Units
2.00
Cost
$645.00