This webinar series provides an introductory yet comprehensive overview of cleaning validation principles and requirements that are crucial for ensuring the effectiveness of cleaning as well as compliance with GMP requirements. Speakers: Vivien Santillan, Director Asia Dr. David Vincent, CEO VTI Lifesciences Learning objective: To understand the Requirement of cleaning validation in GMP To understand…
Novatek will be attending Arab Health 2022 this January. Join Arab Health, at the Dubai World Trade Centre this January, to create meaningful connections and support innovation in healthcare. Get the most out of your participation with the online tool allowing you to start networking before meeting face-to-face in Dubai.
This training course offers a deep dive into the analysis required for Environmental Monitoring (EM) with specific consideration to cGMP and Data Integrity guidelines. As such, the training course is two-fold. The first portion focuses on primarily data analysis for EM. This is for both routine data analysis as well as the analysis required for…
European Annex 1 encourages companies to develop a “Total Contamination Control Strategy” (TCCS). TCCS starts with proper determination of Maximum Safe Carryover (MSC), calculated based on health-based exposure limits (HBELs), a routine cleaning program to evaluate effectiveness of the steps used, followed by microbial Environmental Monitoring, Water and Utilities Monitoring, HVAC filter qualifications, Media Fills,…
Novatek is proud to be an annual sponsor for PDA's Southern California Chapter. All year long, we will be working closely together bringing quality events to our industry peers. Kicking off 2022 with our first sponsored event: PDA SoCal Chapter invites you to attend a Full Day Symposium-Risk Management Risk Management with a focus on…
Novatek will be leading workshops and exhibiting at this year's A3P workshops solely dedicated to the Cleaning Validation process. Full details on the workshop (to be provided in French and English) can be found here: https://www.a3p.org/a3p-validation-nettoyage-2022-lille
The regulations are evolving as are the processes we use to validate and monitor controlled areas and utility systems. Automating these processes and digitizing the data is a must to ensure regulatory compliance and process control. This session will review the regulations regarding the trending and data analysis requirements and which trending tools are applicable…
Novatek is looking forward to exhibiting at Contamin@Lyon this month. Come find us at Booth 14. This year's conference theme is 2022 theme is "The fundamentals of the clean room". All sectors combined, this conferences will deal with essential and varied topics in the world of clean rooms, controlled environments and contaminants.
SAVE $200 off your registration with CODE: Novatek200 55 Tutorials Overflowing with Rich Content and Tangible Takeaways for the CQV Universe Facility Commissioning & Equipment Qualification Implement a Risk-based Verification Strategy Design a Risk-based IQ, OQ, and PQ Approach Manage Process Validation Tech Transfers Qualify Critical Utility Systems – HVAC, Water and Gas Process Validation…
Level Up: Agility in the New Normal This Conference will focus on the theme to Level Up: Agility in the New Normal! We will highlight what’s in store for the future of pharmaceutical manufacturing. Examine how companies are developing new modalities and adapting to the current manufacturing environment through the modernization of aging facilities and the adoption…