August 2020
WEBINAR: Laboratory Information & Quality Management System (LIMS & QMS) for Pharmaceutical Manufacturing
Learn how to increase productivity, compliance and maintaining data integrity through all aspects of pharmaceutical laboratory and quality processes. Thursday August 13, 2020 @ 10 AM-11 AM GMT +7 Register for FREE: https://register.gotowebinar.com/register/609502584626884111?fbclid=IwAR0lltu79FXSU_tMS6RuRy83G1L4_PHdL0FmWqSrvYA072Az9sHXSbtxMB0
Find out more »WEBINAR: Got 15 min? Quick & Straight to the Facts
In response to COVID-19, both Novatek’s Environmental Monitoring Software and NEW Disease Control & Hygiene System are advanced analytical, and data driven technologies that supports effective quality control and reduces risk. Join us as we launch our 15 Minute Webinar Series to deliver quick and "straight to the facts" demonstrations on how to reduce your risk. Contamination Control for Pharmaceutical Manufacturing Part 1: How to Mitigate Risk in Environmental Monitoring for Vaccines & Aseptic Manufacturing - Thurs. June 18, 2020…
Find out more »CONFERENCE HYBRID: Validation & GMP University Philadelphia, PA USA
We are thrilled to be speaking at KENX's Validation University in Philadelphia this year. Join us as we guide attendees on Cleaning Validation Basics and the adoption of an Automated Risk-Based Contamination Control solution. Cleaning Validation Understand Key Elements to a Successful Program Establish Cleaning Residue Limits and Acceptance Criteria Establishing Bioburden and Endotoxin limits for Sterile and Non-sterile Products and Processes Receive a Cleaning Validation Assessment Checklist Example
Find out more »October 2020
CONFERENCE IN PERSON: Aseptic Manufacturing – Maintaining the Validated State Industriens hus, Copenhagen, Denmark
This two-day intensive summit brings together the industry leaders in compliance, aseptic manufacturing and maintaining the validated state. The conference will go beyond presentations on best practice and consists of both presentations and workshops on different aspects of aseptic manufacturing. Attendees will therefore gain a deeper understanding of the new messages from the new Annex 1 draft, FDA focuses on inspecting sterile facilities, sterilization, process validation, life cycle approach and more. The conference will showcase some of the tech that…
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