2019 United States Pharmacopeia (USP) Microbiological General and Information Chapters 7-Part Live Training Program Registration Form:

Program dates are as follows:
Part 1: Tue Apr 2, 2019 - USP <1115> Bioburden Control of Non-Sterile Drug Substances and Products– A New USP General Information Chapter
Part 2: Thu Apr 4, 2019 - USP <51> Antimicrobial Effectiveness Testing – A New 2016 Revised Chapter
Part 3: Tue Apr 30, 2019 - The USP <1113> Microbial Characterization, Identification, and Strain Typing...
Part 4: Thu May 2, 2019 - USP <1072> Disinfectants and Antiseptics - Use and Application of Sanitizers, Disinfectants and Sterilants
Part 5: Tue May 28, 2019 - USP <1116> Microbiological Control and Monitoring of Aseptic Processing Environments and Its Comparison & Contrast to FDA’s Guidance; Aseptic Processing (2004) and Annex 1 (2009)
Part 6: Thu May 30, 2019 - USP <71> Sterility Tests; Method, Limitations, Sampling Quantities and Volumes to Conform with United States Pharmacopeia
Part 7: Tue Jun 25, 2019 - FDA New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices; A Comprehensive Review of the Current Testing Requirements to Include USP <85> Bacterial Endotoxins Test

Each portion of the program will be held at 10:30 AM - 12:30 PM ET (New York Time)

Your registration includes:

• A copy of the copyright presentation slides and/or other reference materials for each registered attendee.
• Answers to your questions during the live presentation.
• Access to a 30 minute live Q&A and consulting session after each live presentation.
• An e-Certificate of Training for each individual attendee’s training records.

* Registration fees are on an individual, per person/attendee basis whether trainees are attending together from a conference room or from separate locations.
* Early registration is strongly recommended as space for each live training webinar is limited to preserve presentation and group participation quality during the live Q&A portion of each live training webinar. All Pharma Webinars live training programs audio and visual are delivered via Cisco WebEx with basic system requirements of a computer with internet access and a telephone to access the audio portion of the presentations. You may choose to access the audio through your computer.

Thank you for choosing Pharma Webinars.


This registration form may not support older versions of Internet Explorer and other browsers. If you are unable to "see" or “Submit” the registration form, you can register via email; View Email Registration Instructions>>> or please call us at Tel: 1 (877) 792-7587 to have one of our associates assist you with the completion of your registration. Thank You.

7-Part Live Training Program Registration Fees:
Single Attendee: $ 1,095.00 - 2 Attendees: $ 1,915.00 - 3 Attendees: $ 2,510.00 - 4 Attendees: $ 3,110.00 - 5 Attendees: $ 3,705.00 - 6 Attendees: $ 4,200.00 - 7 Attendees: $ 4,690.00 - 8 Attendees: $ 5,080.00 - 9 Attendees: $ 5,535.00 - 10 Attendees: $ 6,000.00 - Group over 10 Attendees: $ 495.00 per Attendee


Instrcuctor: Barry A. Friedman Ph.D.

Pharma Webinars Clients:


 "The live webinar was very useful to our team, the content was relevant and the instructor was very knowledgeable" QC Microbiology Supervisor, NJ

  "We were very satisfied with the live presentation; we appreciated the speaker staying on to answer all of our questions" QA Director, MA

  "Our group enjoyed the live presentation and found the experience much more engaging and worthwhile than any recorded webcasts" Sr Training Manager, CA

  "This was my first live training, I found it easy to connect, participate and very useful" Laboratory Analyst, PA

  "We had our entire department attend this training program and found it to be very useful, I am very satisfied with the speaker's ability to keep the audience engaged" QC Manager, NY

  "Given how recent the content of the webinar was, our team members were very happy with the relevance of the training" VP Clinical Operations, CA

  "Is my first time to attend training, I enjoy it very much" Sr Manager, Korea

  "Our department found the level of interactivity between the audience and the instructor far beyond that of any other online training that we have attended before. Well done" Director Regulatory Affairs, ON

  "Our interest group was spread out over three locations and we were able to participate simultaneously and interact very easily" Lead Compliance Manager, IL

  "Well satisfied with the presentation. Our team found the speaker's level of knowledge and his ability to translate that knowledge to our processes very valuable" VP Quality Operations, NC

  "We were impressed with the quality of the presentation, and despite our being located in Europe we were able to participate without a hitch" QC Manager, Ireland