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July 2020


July 20, 2020 @ 8:00 am - July 22, 2020 @ 5:00 pm
Raleigh Convention Center, 500 S Salisbury St
Raleigh, 27601 United States

2020 PDA ANNUAL MEETING Enhancing the Future with Innovative Medicines and Manufacturing Novatek is will be at Booth 205! The theme of the 2020 meeting is Enhancing the Future with Innovative Medicines and Manufacturing. In selecting this theme, the planning committee’s goal is to design a comprehensive event that encompasses the wide-ranging interests of all PDA members. Whether you are focused on improving existing processes or delving into entirely new technologies, we will cover relevant information important to small molecule, and biopharmaceutical,…

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August 2020

2020 Aseptic Processing Course with the PDA

August 10, 2020
|Recurring Event (See all)

One event on August 10, 2020 at 12:00 am

One event on October 26, 2020 at 12:00 am

PDA Training and Research Institute, 4350 East West Highway, Suite 110
Bethesda, MD 20814 United States

Novatek's Associate Director of Product Innovation, Ilona Endisch will contribute for the 3rd year in a row to the 2020 PDA TRI Aseptic Processing Training Courses. Along with other industry leaders, this training course will help you improve your aseptic processes and address contamination control issues that you may encounter. During this training course, you will learn about environmental monitoring systems, facility cleaning and disinfectant qualification, aseptic cleanroom operations, filtration, sterilization, aseptic process simulation (media fill), and regulatory requirements. Hands-on…

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SPEAKER at Validation 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

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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