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    LEARN THE MAIN PRINCIPLES BEHIND A QBD APPROACH AN 2017 - Understanding and Implementing a Quality by Design Program -By AtoZ Compliance

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    Website http://bit.ly/2puMREb | Want to Edit it Edit Freely

    Category fda 510k training, us fda 21 cfr part 820, fda medical device training, fda strategic priorities, fda validation training, pharmaceutical compressed air requirements, clinical quality webinars, qbd training, pharmaceutical training, quality by design pharmaceutical, cgmp training

    Deadline: May 25, 2017 | Date: May 25, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-05-08 19:26:54 (GMT+9)

    Call For Papers - CFP

    Key Take Away:

    This training will explain the main principles behind a QbD approach and provide guidelines on how to implement the concepts into a pharmaceutical development organization.

    Overview:

    The benefits of applying the QbD principles in the pharmaceutical industry have been well advertised. Most important are the direct benefits to our primary customer; the patient. Per Janet Woodcock M.D. Director, Center for Drug Evaluation and Research (CDER), Food and Drug Administration “All products are designed and developed to be of high quality; QbD provides a structured framework for developing, documenting and presenting development rationale, experience and knowledge of the formulation and the process, and to ensure manufacture of products consistently fit for patient use.”

    Application of these principles can also benefit the pharmaceutical companies by improving manufacturing efficiency and promoting innovation. However, implementing these principles into the pharmaceutical development culture can be challenging. QbD involves a complex set of interactions, technologies and systems that are not easy to grasp.

    Why Should You Attend:

    Topics covered will include the target product quality profile, risk assessment, methods to establish a design space, and design of a control strategy. This review will help bridge the gap between understanding the principles and practical application.

    Areas Covered In This Webinar:

    QbD principles discussed include

    Quality Target Product Profile (QTPP)

    Risk Assessment

    Using Models

    Design of Experiments

    Developing a Design Space

    Process Analytical Technology (PAT)

    FMEA and Control Plan

    Target Operational Profile

    Control Strategy

    Learning Objectives:

    Prepare individuals to better understand the principles behind using QbD to develop a pharmaceutical product

    Understand what is meant by Quality be Design

    Understand the benefits from applying a QbD approach

    Provide key steps to implement a QbD program

    Understand what the important tools used to implement a QbD approach

    Who Will Benefit:

    This course is designed for people tasked with developing, filing, and manufacturing pharmaceutical products especially small molecule oral dosage forms. This includes individuals that have responsibilities for formulation development, scale-up, filing, and commercial manufacture of dosage forms as well as maintaining the high quality of those products. Following personnel will benefit from the course:

    Senior quality managers

    Quality professionals

    Regulatory professionals

    Compliance professionals

    Production supervisors

    Manufacturing engineers

    Production engineers

    Process owners

    Quality engineers

    Quality auditors

    Development professionals

    Senior development managers

    Level:

    Intermediate

    For more information, please visit : http://bit.ly/2puMREb

    Email: supportatatozcompliance.com

    Toll Free: +1- 844-414-1400

    Tel: +1-516-900-5509

    Speakers Profile :

    Steven Laurenz

    Steven Laurenz– Chemical Engineering M.S. – Michigan State University

    Expertise: Over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. Skilled in taking new products from early laboratory stage to successful manufacturing launch. Expert in integrating Quality by Design and risk management into product development. Experience in establishing a Quality System for a R&D Quality Assurance organization.

    Experience: Headed product development departments at Abbott Laboratories and AbbVie Inc. Leadership positions in numerous technical consortiums.

    Other: Black Belt certified in Business Excellence and Master Certificate in Applied Statistics


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.