October 2021
Podium Speaker: 2021 PDA Pharmaceutical Microbiology Conference
Novatek is proud to be a podium speaker at this year's Microbiology Conference hosted by PDA! This Conference continues the ongoing tradition of addressing the opportunities and challenges, most relevant, to the future of microbiology in today’s global market. Join new and seasoned professionals from all facets of the field, including global industry, academia, and regulatory authorities, to share insights on how to best prepare for the future through the sharing of best practices, development of standards, and integration of…
Find out more »IPA Annual GMP Update | BPF Mise à jour Conference 2021
Novatek is proud to return as a speaker to IPA's GMP Update! About the Conference International Pharmaceutical Academy (IPA) is delighted to be hosting its 17th annual GMP Update | BPF Mise à jour on October 6 & 13, 2021 | Online. This virtual conference will provide attendees with insight and a plethora of information on quality, compliance, validation, and regulatory areas affecting the pharmaceutical, biopharmaceutical and allied industries. It will address…
Find out more »Speaker: IVT Validation Week Hybrid Event
The gold-standard event for validation and quality professionals across the life sciences, providing critical information on new regulations, industry best practices and technological advancements. Bringing together highly-recognized experts for benchmarking and knowledge on the most critical topics in process validation, computer system validation, cleaning validation, equipment qualification, data integrity and more, this event is a must-attend. Novatek will be both speaking and sponsoring this year's event: Presentation Tools & Technologies: Annex 1 Contamination Control – What the Recent Revision Means…
Find out more »November 2021
Conference: ISPE Annual Meeting & Expo
Agility. Collaboration. Innovation. The 2021 ISPE Annual Meeting & Expo will usher in a revitalized focus on excellence, modernization, and harmonization in pharmaceutical science and manufacturing across the globe, offering pharma professionals the opportunity to engage in industry-critical conversations. A comprehensive education program provides attendees with technical sessions on the latest developments in supply chain, operations, facilities, equipment, information systems, product development, production systems, quality systems, regulatory guidance and cutting-edge industry innovations. This signature event draws pharmaceutical and biopharmaceutical professionals at all…
Find out more »Speaker: Aseptic Manufacturing – Maintaining the validated state – Key2Compliance®
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, sterilisation, process validation, life cycle approach and more. The conference will showcase some of the tech that…
Find out more »PDA West Coast Chapter: Micro Event
Novatek is proud to be an annual sponsor and speaker for PDA's West Coast Chapter! We will be both sponsoring and speaking at this November's MICRO EVENT! More details to be found here: https://www.pda.org/global-event-calendar/event-detail/pda-west-coast-chapter-micro-event
Find out more »Speaker: Science, Risk and Statistics-based Cleaning Process Development & Validation -Key2Compliance®
This two-day, intensive virtual conference brings together the industry leaders on Science and Risk- and Statistics-based Cleaning Process Development and Validation. The conference will go beyond presentations on best practice and consists of workshops complemented with plenary Q&As. Attendees will therefore gain a deeper understanding of the new ASTM E3106 Standard, PDA TR 29 revision, Annex 1, HBELs, new draft and use of statistics in cleaning validation, as well as risk evaluation and data integrity in cleaning validation – among…
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