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ICH Q11- API Manufacturing - 2017

  April 18, 2017  
Compliance4All, Online

This webinar will address approaches to developing and understanding the

manufacturing process for a drug substance. The information obtained will

enable completion of the drug substance information in Module 3 of a CTD


Why should you Attend:
This presentation is presented in practical language understandable by all

technically educated or trained individuals, regardless of specialty.

Areas Covered in the Session:
    Manufacturing process development
    Process controls
    Selection of starting materials
    Control strategy
    Process validation evaluation
    Submission of information
    Life cycle management

Who Will Benefit:
    Quality Assurance
    Quality Control (Chem and Micro)
    Process and Design Engineering
    Process Automation
    Manufacturing Operations
    Utility Operations

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Organized by: Compliance4All
Invited Speakers: Speaker Profile:
Peggy J. Berry , MBA, RAC, is the President & CEO at Synergy Consulting

where she provides consulting services to companies in all aspects of drug

development. She also provides group and one-on-one training in drug

development, regulatory affairs and project management topics.
Deadline for Abstracts: 2017-06-21

Full Details & Registration Link:


E-mail: support@compliance4All.com
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