2019 Annual Pharmaceutical Impurities Training Program 4-Part Live Training Program Registration Form:

Program dates are as follows:
Part 1 - Wed January 30,2019 - FDA Guideline on Analytical Procedures and Method Validation with Application to Impurities
Part 2 - Wed February 27, 2019 - Understanding the Impact of FDA, ICH, USP and EMEA impurity guidelines, and data needed to establish acceptance criteria according to the FDA Manual of Policy and Procedure (MAPP)
Part 3 - Wed March 27, 2019 - Elemental Impurities – Understanding and Implementing USP General Chapters <232> and <233>
Part 4 - Wed April 24, 2019 - Monitoring Organic Impurities in Pharmaceutical Products to Meet FDA and ICH Q3 A/B Requirements
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.

4-Part Live Training Program Registration Fees:
Single Attendee: $ 1,195.00 - 2 Attendees: $ 1,570.00 - 3 Attendees: $ 2,200.00 - 4 Attendees: $ 2,840.00 - 5 Attendees: $ 3,275.00 - 6 Attendees: $ 3,700.00 - 7 Attendees: $ 3,850.00 - 8 Attendees: $ 4,100.00 - 9 Attendees: $ 4,375.00 - 10 Attendees: $ 4,450.00 - Over 10 Attendees: $ 410.00 per Attendee

 
 Instructor: Kim Huynh-Ba

Instructors:
Kim Huynh-Ba & Anthony J. DeStefano Ph.D.

Pharma Webinars Clients:

Testimonials:

 "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