PHARMA WEBINARS

Interactive, Instructor-Led Training Webinars

Every Live Webinar Benefits from 30 Minutes of Live Q&A

Engaging and Informative

Regularly Updated Content Provides the Latest Regulatory, Operational and Technological Information in the Pharmaceutical Arena

Delivered Live by Recognized Subject Matter Experts

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PHARMA WEBINARS

Pharma Webinars is revolutionizing the technical training experience for the pharmaceutical industry. Our unique approach to designing and delivering live instructor-led online training programs by prominent industry experts in their respective fields provides practical perspectives from the highest qualified sources.
Our innovative "live only" training approach sets Pharma Webinars apart from the rest of the field and allows us to offer industry unique material in a format that enables us to ensure that content is relevant and updated. Pharma Webinars live training programs are facilitated by prominent industry experts in their respective fields providing practical perspectives from the highest qualified sources... Learn More >


Client 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

Live Training Benefits:

• Designed and delivered based on e-learning best practices
• Interactive, instructor-led live training programs.
• Engaging and informative live presentations allowing trainees to exchange ideas during presentation in real time.
• Each live training webinar includes a 30 minute Q&A period enabling trainees to interact directly with the instructor.
• Pharma Webinars' instructors are the most recognized subject matter experts in the industry who are selected based on very strict qualification criteria.
• Each Pharma Webinars live training webinar and program content is updated on regular basis to provide the latest regulatory, operational and technological trends in the international pharmaceutical arena... Learn More>>>

 

Featured Live Training Webinars:

Annual Product Quality Reviews; Preparation & Reports - FDA, EU, & Canada Regulatory Requirements and the Impact of the New FDA Quality Metrics Guidance on Annual Product Reviews
Live Training Webinar - Date: Wednesday December 12, 2018 - Time: 9:30 - 11:30 AM ET (New York Time)
Instructor: Jerry Lanese Ph.D. Detailed Information>>>


GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry Including a Review of the New 2018 MHRA Data Integrity Definitions & Guidances and the FDA’s Most Recent Draft Guidance
Live Training Webinar - Date: Thursday December 13, 2018 - Time: 9:30 - 11:30 AM ET (New York Time)
Instructor: Peter Calcott Ph.D. Detailed Information>>>


Managing Microbiological Out of Specification (OOS) and Out of Trend (OOT) Results in Sterile and Non-Sterile Production– FDA & ICH Expectations and Guidance
Live Training Webinar - Date: Tuesday December 18, 2018 - Time: 10:30 AM - 12:30 PM ET (New York Time)
Instructor: Barry Friedman Ph.D. Detailed Information>>>


Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations
Live Training Webinar - Date: Wednesday December 19, 2018 - Time: 9:30 - 11:30 AM ET (New York Time)
Instructor: Jerry Lanese Ph.D. Detailed Information>>>


Laboratory Quality Practices for Global Regulatory CMC Analytical Studies for Biotechnology/Biosimilar Products: R&D to GMP
Live Training Webinar - Date: Wednesday January 16, 2019 - Time: 10:30 AM - 12:30 PM (Eastern New York Time)
Instructor: Nadine M. Ritter Ph.D. Detailed Information>>>


Current FDA and Global cGMP Compliance Requirements and Guidances for In-House and Contract Analytical QC Laboratories; Understanding the Unique Elements of cGMP Applicable to QC Analytical Testing Laboratories
Live Training Webinar - Date: Thursday January 17, 2019 - Time: 10:30 AM - 12:30 PM ET (New York Time)
Instructor: Nadine M. Ritter Ph.D. Detailed Information>>>


Risk Management of Raw Materials in a GMP Environment – Developing an Effective Strategy for Testing Raw Materials in Phase 1 Through Phase 3 Environment
Live Training Webinar - Date: Wednesday January 23, 2019 - Time: 10:30 AM - 12:30 PM ET (New York Time)
Instructor: Barry Friedman Ph.D. Detailed Information>>>


Use and Application of Sanitizers, Disinfectants and Sterilants in a GMP Controlled and Classified Environment, Key Elements of a Robust Cleaning and Disinfection Program & Latest USP and FDA Requirements
2-Part Live Training Program - Instructor: Barry A. Friedman Ph.D.

Part 1: Use and Application of Sanitizers, Disinfectants and Sterilants in a GMP Controlled and Classified Environment – Latest Regulatory Requirements & Guidance
Live Training Webinar - Date: Thursday January 24, 2019

Part 2: Development and Implementation of a Robust Cleaning and Disinfection Program & The Use of USP<1072>, <1227> and <51> within the Development of Disinfectant Efficacy Programs
Live Training Webinar - Date: Thursday January 31, 2019

2-Part Live Training Program Time: 10:30 AM - 12:30 PM ET (New York Time)

Detailed 2-Part Live Training Program Agenda>>>


2019 Annual Pharmaceutical Impurities Training Program

4-Part Live Training Program - Instructors: Kim Huynh-Ba and Anthony J. DeStefano Ph.D.

Part 1: FDA Guideline on Analytical Procedures and Method Validation with Application to Impurities
Live Training Webinar - Date: Wednesday January 30, 2019

Part 2: 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)
Live Training Webinar - Date: Wednesday February 27, 2019

Part 3: Elemental Impurities Compliance for the Pharmaceutical Industry; Understanding and Implementing USP General Chapters <232> & <233> and A Review of ICH Q3D
Live Training Webinar - Date: Wednesday March 27, 2019

Part 4 : Monitoring Organic Impurities in Pharmaceutical Products to Meet FDA and ICH Q3 A/B Requirements
Live Training Webinar - Wednesday April 24, 2019

Detailed 4-Part Live Training Program Agenda>>>


 
 

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