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August 2020

WEBINAR: Laboratory Information & Quality Management System (LIMS & QMS) for Pharmaceutical Manufacturing

August 13, 2020 @ 10:00 am - 11:00 am
novatek international event

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

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WEBINAR: Got 15 min? Quick & Straight to the Facts

August 13, 2020 @ 1:00 pm - 1:15 pm
|Recurring Event (See all)

One event on June 30, 2020 at 1:00 pm

One event on July 16, 2020 at 1:00 pm

One event on July 23, 2020 at 1:00 pm

One event on July 30, 2020 at 1:00 pm

One event on August 6, 2020 at 1:00 pm

One event on August 13, 2020 at 1:00 pm

novatek international event

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…

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CONFERENCE HYBRID: Validation & GMP University Philadelphia, PA USA

August 24, 2020 @ 8:00 am - August 26, 2020 @ 5:00 pm
Wyndham Philadelphia Historic District, 400 Arch Street
Philadelphia, PA 19106 United States
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novatek international event

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

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October 2020

CONFERENCE IN PERSON: Aseptic Manufacturing – Maintaining the Validated State Industriens hus, Copenhagen, Denmark

October 21, 2020 @ 8:00 am - October 22, 2020 @ 5:00 pm
Industriens hus, H.C. Andersens Blvd. 18 Copenhagen Denmark + Google Map
novatek international event

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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