Annual Current Good Manufacturing Practices (cGMP) Training.

Todd Graham

Starting at

$349


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This webinar provides a basic understanding and fundamental principles of Current Good Manufacturing Practices and will fulfill the requirement of personnel involved in cGMP must have documented training of current Good Manufacturing Practices. This session will focus on the FDC Act and 21 CFR federal regulations as applied to cGMP.

Why Should You Attend:

Good Manufacturing Practice regulations, which have the force of law, require that manufacturers, processors, and packagers of medicinal products take proactive steps to ensure that their products are safe, pure, and effective. cGMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mix-ups, and errors.

Personnel involved in cGMP must have documented training of current Good Manufacturing Practices (cGMP) training. This webinar will focus on the FDC Act and 21CFR federal regulations as applied to cGMP and provide an overview of the US FDA regulations for compliance.

Areas Covered in the Webinar:

  • What is cGMP and why is it important; Brief history of drug manufacturing
  • Describe the federal regulations applied to cGMP and inspections
  • Discuss: Organization and Personnel, Building and Facilities, Equipment, Production and Process control, Laboratory, Quality, Documentation
  • Review listing of guidelines as apply to cGMP
  • Terms and Definitions

Who Will Benefit:

This webinar will be beneficial for all personnel involved in the manufacturing, packaging, labeling, storage, testing, and distributing of medicinal products in US. Personnel in the following roles can especially benefit from the presentation:

  • Quality and Compliance
  • Manufacturing and Packaging
  • IT
  • Operations
  • R&D
  • Equipment, Facilities and Process Engineering Documentation
Webinar Events
Live -Coming soon!

Training CD-DVD

Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment


Recorded video

Recorded video session



Speaker: Todd Graham,

Todd Graham , is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertise are molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He is also in the process of establishing a consultancy that assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.


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