This training course integrates the in-vitro dissolution testing, equipment requirements, quality control aspects and using dissolution to obtain biowaivers.

    Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers

    14 – 16 February 2022, live online training

    Summary

    A unique online training course that integrates the in-vitro dissolution testing, equipment requirements, quality control aspects and using dissolution to obtain biowaivers.

    Learning Objectives

    • The role of dissolution studies and dissolution equipment
    • Connecting the dissolution data to pharmacokinetics
    • Quality control aspects of dissolution testing
    • How to develop dissolution tests and how to interpret them
    • About the requirements for studies in fasting and fed state
    • How to obtain biowaivers with the use of dissolution studies

    Key Topics

    • Why do we need Dissolution?
    • Development of dissolution tests
    • Dissolution test equipment and its constraints
    • QC aspects of dissolution testing
    • Dissolution testing in stability testing
    • Use of dissolution studies to obtain biowaivers

    Who should attend?

    Dissolution testing specialists, BA/BE managers, Pharmacokineticists, IVIVC scientists, Regulatory affairs managers, R&D scientists, QC and QA managers

    Past participants

    • Global Clinical Project Manager, Gedeon Richter
    • Manager Clinical Affairs, Stada
    • Head of Research and Development, Medichem
    • IVIVC and AD Researcher, Lek – A Sandoz Company
    • Analytical Development Scientist, Catalent

    Our online training experience includes

    • Our client zone – a single source for all training materials as well as pre and post-training communication
    • Live interactive format via the Zoom platform
    • Direct interaction with the trainer
    • Q&As, case studies, polls
    • Revisit recorded sessions for 30 days
    • Training in digital format
    • Digital and LinkedIn certificates

    Trainers

    Generapharm, CEO
    Dr. Ross has over 35 years experience in the Generics Industry, the last 15 being at corporate level. He has been intimately involved in strategic planning, pipeline management and related activities.
    Online Participation
    1 650  Price incl. VAT: 1 650 
    Equivalent of approx. 1 769 USD.
    The price calculation in USD is informative and might slightly differ from your bank exchange rate
    .

    Price per delegate including:

    Online participation

    Online workbook & materials

    Certificate

    PC, microphone, camera, stable internet connection and the Zoom application.

    Yes, we will make every effort to ensure best possible interaction. You will see the slides, interact with the trainer and fellow participants. Questions and group exercises will be facilitated through the online meeting platform.

    Yes, you can transfer the registration to a colleague at any time.

    Yes, you may transfer your registration to a different event up to one month before the scheduled dates, provided the training fee has been paid in full.

    pharma learning leader

    Lydia Makori

    l.makori@symmetric.events
    +421 222 200 543

    Training Details
    What participants said about this course

    "You succeed only when you are trained enough! Trust Symmetric's Training Team to achieve your goals"
    Analytical Developer, Gedeon Richter

    “I enjoyed the trainer's very all-round experience and expertise. He was far from "just" an analytical scientist”
    Product Development Manager, Pharmanovia

    “Excellent examples of dissolution failure from the real-world."
    Associate QC Analyst, Genera

    “The style and the deep knowledge of the presenter Dr. Malcolm Ross. He was very good!”
    Head of Solid State, Seqens