Pharmaceuticals FDA-cGMP Training (21CFR210-211) PD631848

The FDA requires employees to be trained in the current good manufacturing practice 21CFR210-211 as they relate to the employee's  functions to help assure the safety and efficacy of drug products. 

Objectives

• Understanding the current regulations: Gain a comprehensive understanding of the current Good Manufacturing Practices (cGMP) regulations as outlined by the FDA, particularly focusing on Title 21 CFR Parts 210 and 211.
• Compliance with regulatory requirements: Learn how to interpret and apply the regulations to ensure compliance within the pharmaceutical manufacturing environment.

Materials Provided

• 365 days of online single-user access (from date of purchase) to the approximately 15 hours of instruction
• Continuous assessment to check knowledge and application of key concepts
• Follow-up to your content questions

Is this On Demand Course for You?

This course is intended for employees in pharmacies and pharmaceutical companies who need to be trained in cGMP regulations and individuals seeking to learn about the FDA's 2016 version of cGMP for finished pharmaceuticals.

For More Details

Email CustomerService@sae.org, or call 1-877-606-7323 (U.S. and Canada) or 724-776-4970 (outside US and Canada).