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  • Blank-4
    Monday, March 11, 2024 · 4:00 PM CET
    This webinar provides an overview about inspection trends and latest industry guidelines in 2023 (and beyond).
    We will check FDA's inspection database and uncover some recurring inspection topics in 483s and Warning Letters such as Vigilant Monit...
  • Blank-6
    Thursday, February 29, 2024 · 4:00 PM CET
    Almost 2 years after we hosted our first Data Integrity in GCP Webinar, many things have changed with regards to regulatory expectations for the design and conduct of clinical trials while others remain as before. The latest revision to ICH E6 (R3...
  • Blank-2
    Thursday, November 16, 2023 · 4:00 PM CET
    ICH Q9 established a framework for QRM with the intention of introducing QRM approaches that could be leveraged by both the industry and regulators. However, it has been observed that the full potential of QRM has not been reached, which is the re...
  • Monday, September 25, 2023 · 4:00 PM CEST
    Dieses kostenlose Webinar gibt einen Einblick in die Anforderungen und die Voraussetzungen einer erfolgreichen CBD Produktion im GMP-Umfeld. Wir geben einen Überblick über Begriffe und Definitionen, welche Regelungen (Good Agricutural and Cultivat...
  • Thursday, September 14, 2023 · 4:00 PM CEST
    Dieses kostenlose Webinar gibt einen Einblick in die Faktoren zur Datenintegrität in der Life Science Produktion. Wir geben einen Überblick über aktuelle Guidelines wie PDA's TR 84 und ISPE Good Practice Guide on Manufacturing Records.

    Das sich s...
  • Tuesday, August 15, 2023 · 4:00 PM CEST
    Join us as we delve into the transformative role of Artificial Intelligence (AI) in the pharmaceutical and healthcare industry. Discover the existing guidance, effective data management strategies, and crucial validation activities essential for s...
  • Blank-2
    Tuesday, July 4, 2023 · 4:00 PM CEST
    Data integrity programs often suffer from a severe blindspot: They do not focus on the "soft facts", the human factors!
    An intact quality culture is a key enabler together with a strong data governance program to derive Data Integrity and fullfil...
  • Thursday, June 22, 2023 · 4:00 PM CEST
    In this engaging and informative webinar, we will explore the essential task of overcoming lab compliance challenges. Our experts will explore the intricacies of maintaining efficient operations in the laboratory environment while complying with r...
  • Wednesday, May 24, 2023 · 4:30 PM CEST
    The Life Science Industry holds highly sensitive and confidential data, making it a prime target for cybercriminals. In this presentation, "Shielding Critical Life Sciences Data from Cyber Threats" we will provide an overview of the current cybers...
  • Thursday, March 23, 2023 · 4:30 PM CET
    THE WEBINAR IS FULL - IF YOU WANT TO ASK FOR ANOTHER OPPORTUNITY TO PARTICIPATE, PLEASE REACH OUT TO:
    ulrich.koellisch@gxp-cc.com

    This free webinar will provide insights into data integrity considerations in life science manufacturing operations...
  • Wednesday, October 19, 2022 · 4:00 PM CEST
    In this Data Integrity GCP part 2 FREE webinar, Dr. Thaleia Papadopoulou, Dr. Ulrich Köllisch and Milena Gjorgjieva will highlight the importance of Data Integrity in GCP, and risks associated with clinical studies by presenting real-life case stu...
  • Wednesday, July 13, 2022 · 4:00 PM CEST
    In this FREE webinar, Dr. Thaleia Papadopoulou and Dr. Ulrich Köllisch highlight the Data Integrity challenges and risks associated with clinical studies. Recent guidelines like the EMA Draft guideline will be discussed, real-life case studies wi...
Past
  • Blank-4
    Tuesday, December 5, 2023 · 10:00 PM CET
  • Tuesday, May 25, 2021 · 4:00 PM CEST
    Robotic process automation (RPA) software is available to assist Pharma by reducing the time to market, costs in production and improving the management of the compliance requirements, but it also requires a lean and solid validation life cycle to...
  • Tuesday, April 27, 2021 · 3:00 PM CEST
    Get to know about digital transformation with BLOCKCHAIN and learn what to consider in regulatory environments.
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