Process Scale-up and Technology Transfer for Injectables - Live Online Training

    Process Scale-up & Tech Transfer for Injectables

    17 – 19 October 2022, live online training

    Summary

    This three-day online training course is providing vital practical insights into QbD implemented Process Scale-up, Technology Transfer, and Process Validation for sterile injectable dosage forms.

    Learning Objectives

    • Understand industry approaches for Scale-up, Tech Transfer and PV applying QbD principles
    • Explore proven best practice in Scale-up and Tech transfer for sterile injectables
    • Take an excellent opportunity to discuss issues and challenges with industry peers
    • Gain practical knowledge from case studies

    Key Topics

    • QbD Principles during Process Development and Scale-Up
    • Process Scale-Up of sterile injectable dosage forms
    • Technology Transfer: Regulatory, Planning & Execution
    • Process Validation new guidance and requirements
    • Process Design Stage
    • Process Performance Qualification
    • Continued Process Verification
    • Process risk assessment

    Who should attend?

    Injectables Technologists, Process Scientists, Process Engineers, Process Validation Specialists, CMO Managers, Technology Transfer Specialists, Manufacturing Management, Regulatory Affairs Managers, QC & QA Managers

    Past participants

    • Drug Product Subject Matter Expert, Pfizer
    • CMC Project Manager, Britannia Pharmaceuticals
    • Formulation Development Coordinator, Boehringer Ingelheim
    • Project Coordinator, Ferring Pharmaceuticals

    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
    • Digital and LinkedIn certificates

    Trainers

    Protea, CEO
    Laura has an extensive industrial experience in the development of drug products for the worldwide market, from scratch to registration, in accordance with GxP and ICH requirements.

    Process Scale-up & Tech Transfer for Injectables

    Download the full training agenda to reveal complete session details, training takeaways, case studies, daily schedule, special features and full trainer bio.

    Online Participation 17-19 Oct 2022
    1 650  Price incl. VAT: 1 650 
    Equivalent of approx. 1 777 USD.
    The price calculation in USD is informative and might slightly differ from your bank exchange rate
    .

    Price per delegate includes:

    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
    • Start Date
      17. October 2022
      09:00 AM Vienna time
      08:00 AM London time
      03:00 AM New York time
      12:00 AM Los Angeles time
    • End Date
      19. October 2022
    What participants said about this course

    "Many thanks for the invitation, organization of the training and the atmosphere. I found the course very well organised and presented."
    Formulation Manager, Curia

    "I appreciatte the case studies and examples that could be applied at my job."
    Project Manager, Fresenius Kabi

    "The break out groups were great way to work on case studies."
    Process Engineering Manager, Cenexi

    "The trainer's expertise and preparation were great. The questions from the participants and the answers/discussions from the trainer were very helpful."
    Product Technology And Transfers Manager, Zentiva

    "The trainer was very knowledgeable about the topics and was able to answer all questions."
    Drug Product Subject Matter Expert, Pfizer

    "Case studies were very relevant to my work. Content cover was great and well distributed."
    Senior Specialist, Bavarian Nordic

    "That the presentation had a flow, and there were discussed topics from development to validation."
    Regulatory Affairs Senior Officer, Generis Farmacêutica

    "The case studies and the work in the breakout sessions. The trainer was open to specific case questions and allowed for sufficient discussion."
    Manufacturing Supervisor, Curia

    "Great overview on parenterals and the whole environment!"
    Project Coordinator, Ferring Pharmaceuticals