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Recorded Webinars
Harold Thibodeaux

SOPs for Clinical Trials: Regulatory Requirements

Since the year 2000 there has been an increasing trend of registered clinical studies from approximately 4,000 in 2000 to 160,000 in 2014. In 2014 Forbes Magazine reported that the FDA had approved 44 drugs the highest in 18 years.

Speaker: Harold Thibodeaux | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Harold Thibodeaux

FDA New Drug Approval Process

In the calendar year 2015, the pharmaceutical industry witnessed the largest number of Food and Drug Administration (FDA) prescription drug approvals in the past decade. The FDA's Center for Drug Evaluation and Research played a valuable and key role in bringing these drugs to market.

Speaker: Harold Thibodeaux | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Harold Thibodeaux

Research Use Only Products - The Dos and Don'ts

For medical professionals involved with clinical development of drugs and medical devices, they are well educated that the Food and Drug Administration (FDA) is the regulating agency that provides the regulatory requirements necessary for final approval.

Speaker: Harold Thibodeaux | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
Harold Thibodeaux

SOPs for Clinical Trials: Regulatory Requirements

Since the year 2000 there has been an increasing trend of registered clinical studies from approximately 4,000 in 2000 to 160,000 in 2014. In 2014 Forbes Magazine reported that the FDA had approved 44 drugs the highest in 18 years.

Speaker: Harold Thibodeaux | View Anytime | Duration: 90 Minutes | Price: ¤190.00 | View Details
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