2019 Advanced Pharmaceutical Cleaning Validation 11-Part Training Program Registration Form:
You may register for the remaining 10 parts of this 11-part live training program.

Program dates are as follows:
Part 1: Tuesday June 18, 2019 - Examining Regulatory Requirements for: Cleaning Validation Overview, Life Cycle Approach for Cleaning Validation, Design and Development of Cleaning Processes and Cleaning Validation Protocols and Reports (Completed)
Part 2: Tuesday July 16, 2019 - Examining Regulatory Requirements for: Setting Limits and Analytical Methods and Method Validation
Part 3: Tuesday August 13, 2019 - Examining Regulatory Requirements for: Sampling and Sampling Recovery, Dirty Hold Time, Clean Hold Time, Microbiological Issues and Validation Maintenance
Part 4: Tuesday September 24, 2019 - Cleaning Validation; Utilizing “Health-Based” Limits, Toxicological Evaluation VS. Dose-Base Criterion, Examination of ISPE Approach and EMA’s New Dedication Guidance
Part 5: Thursday September 26, 2019 - Utilizing “Health-Based” Limits for Cleaning Validation; Practical Considerations in Implementing “Health-Based” Limits into Protocols
Part 6: Tuesday October 22, 2019 - Cleaning Validation; Dealing with “Indirect Product Contact Surfaces” and “Non-Product Contact Surfaces” & Regulatory Recommendations
Part 7: Thursday October 24, 2019 - Cleaning Validation; Issues in the Use of Total Organic Carbon (TOC) as an Analytical Technique
Part 8: Tuesday November 19, 2019 - Cleaning Validation; Understanding Variations on Expression of Limits and Special Cases in Setting Residue Limits & Regulatory Concerns
Part 9: Thursday November 21, 2019 - Cleaning Validation; Design of Automated & Manual Cleaning Processes & Latest Regulatory Requirements
Part 10: Tuesday December 10, 2019 - Cleaning Validation: Issues in the Validation of Manual and Automated Cleaning Processes & Latest Regulatory References
Part 11: Thursday December 12, 2019 - Cleaning Validation: Dealing with Dedicated Equipment and with Campaigns

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.

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or please call us at Tel: 1 (877) 792-7587 or send us an email to support@pharmawebinars.com to have one of our associates assist you with the completion of your registration. Thank You.

Instructor: Destin A. LeBlanc

Instructor: Destin A. LeBlanc


Pharma Webinars Clients:


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