Overview

Aseptically processing final drug product is a crucial step in the drug manufacturing process. Failures related to aseptic processing of a final drug product are detrimental to patients. In many cases, once a failure is discovered, the drug product is considered unfit for use and may be destroyed. By understanding and implementing the concepts described in the Aseptic Guidance document, – Sep 2004, many of the failures related to aseptic processing can be eliminated.

The process of aseptic filling final drug products is not an easy task. The FDA Aseptic Processing Guidance document gives guidance when it comes putting the proper procedures and controls into place for preventing harm to a patient related to aseptic processing. By understanding how final drug product is aseptically processed, pharmaceutical companies can implement many of the controls described in the FDA Guidance Document.

Webinar Takeaway

  • Brief history of reason why the Aseptic processing guidance document is important,
  • Brief overview of the Aseptic Processing Guidance Document – Sep 2004.
  • Reviewing the concepts outlined in the Aseptic Guidance document and ways to implement the concepts described in the guidance document.
  • Examples on how the concepts outlined in the Aseptic Processing Guidance document can be implemented.

Who Will Benefit

  • Quality Assurance Managers and Directors
  • Quality Control Personnel
  • Supervisors, and Managers involved in Compounding Drug Products
  • Consultants
  • Regulatory and Compliance Management
  • Regulatory Affairs Professionals

Industries who can attend

This 60 -minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.

Faculty Carl Patterson

Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However, his avid interest in all things biology, microbiology, and biochemistry officially began when he served in the U.S. Army as a Preventative Medicine Specialist and a Licensed Vocational Nurse. Furthermore, Carl holds various degrees and certifications, including an M.S. in Biomedical Quality Systems from San Diego State University, a B.S. in Microbiology from the University of Texas, and Specialized Certificates in QA/QC & Biotechnology from UCSD.

Faculty Carl Patterson

Choose a Purchase Options

$289

Recorded Access Single - 6 month Access

You'll have access to one log-in for an archived recording of the entire 60-minute webinar, including the Q&A period, for 1 participant. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

$399

MP3 Download (DVD)

Within 48 hours delivered - Lifetime Access ,Audio recording of a webinar and reference manual delivered by download. Listen anytime on any compatible device.