2019 Annual Pharmaceutical GMP 8-Part Live Training Program Registration Form:

Program dates are as follows:
Part 1: Tuesday March 12, 2019 - Quality Management System (QMS) – The New FDA, EU and Global Regulatory Requirements, Maintaining the Validated State and Driving for Consistency
Part 2: Thursday March 14, 2019 - Quality Management System (QMS) – Handling Deviations and Out-of-Spec (OOS) Investigations Based on the Latest FDA, EMA and Global Regulatory Requirements
Part 3: Tuesday April 9, 2019 - Quality Management System (QMS) – The New QMS Paradigm Explained
Part 4: Thursday April 11, 2019 - Facilities and Equipment; Linking the Latest FDA , EMA and Other Regulatory Bodies' Regulatory Expectations With Respect to Design, Construction, Start Up and Commissioning of Facilities and Utilities to Best Practices
Part 5: Tuesday May 7, 2019 - Latest FDA EMA & Other Regulatory Requirements of Pharmaceutical Manufacturing; from Manufacturing of Bulk Drugs to Finished Product Including Packaging and Labeling Activities
Part 6: Thursday May 9, 2019 - Key GMP Requirements of Pharmaceutical Laboratories – Understanding the Latest FDA & Global Regulatory Requirements
Part 7: Tuesday June 11, 2019 - Raw Materials and Components Management – Latest Regulatory Requirements including a Review of the EMA Falsified Medicines Directive, Food and Drug Administration Safety and Integrity Act (FDAsia), Drug Supply Chain Security Act (DSCSA), & Secure Supply Chain Pilot Program (SSCPP)
Part 8: Thursday June 13, 2019 - GMP Requirements for Records and Reports – Documenting Your GMP Activities; Understanding the Vital GMP Requirements of a Documentation System
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.

8-Part Live Training Program Registration Fees:
Single Attendee: $ 1,295.00 - 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: $ 585.00 per Attendee

 
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Instructor: Kim Huynh-Ba & Peter Calcott 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