Page 2 – Novatek International

You are here:

The Importance of Stability Studies in Pharmaceutical Manufacturing In pharmaceutical manufacturing, ensuring drug product stability is essential for maintaining GMP compliance, quality control, and long-term patient safety. Robust stability studies help manufacturers understand degradation, support accurate shelf-life predictions, and generate the validated data needed for FDA/ICH regulatory submissions. Today’s leading organizations are adopting…

Details

Stability Testing in Pharma with Optimized Statistics

Articles, Journal and Publications, News, Novatek Experts Blog, Resources, White PapersBy Jadzia Famili November 26, 2025

Susan Cleary Susan B. Cleary, B.Cs, EMBA. Director of Product Development Stability Testing in Pharma: In pharmaceutical manufacturing, ensuring drug product stability is essential for maintaining GMP compliance, quality control, and long-term patient safety. Robust stability studies help manufacturers understand degradation, support accurate shelf-life predictions, and generate the validated data needed for FDA/ICH regulatory submissions.…

Details

PharmaLab

By Jadzia Famili November 7, 2025

Join Parsa Famili’s talk on November 24-26 in Dusseldorf. Come find Sarah Alimirzaei on-site! The event for all pharmaceutical laboratory sectors will take place for the 13th time from 24-26 November 2025 – on site in Düsseldorf/Neuss. The PharmaLab 2025 conferences will cover various topics and lectures on analytics, bioanalytics and microbiology. Parallel to the conferences, participants…

Details

Speak Pharma – 2nd Cleaning Process & Validation Conference

By Jadzia Famili November 7, 2025

Join Susan Cleary, Ilona Endisch, and Angel Ruiz on November 19-20 in Prague. Speak Pharma presents the 2nd edition, scheduled in the beautiful city of Prague, Czech Republic, and online on November 19-20, 2025. Industry leaders will explore critical aspects of safe pharmaceutical manufacturing, “equipment design for rapid and robust CIP (Clean in Place)…

Details

KENX – AI in GxP Europe

By Jadzia Famili November 7, 2025

Join Parsa Famili and Niccolo Moreno on November 19-20 in Dublin, Ireland. Welcome to Harness the Power of AI in GxP Europe Use Cases, Process Optimization, and Validation, in beautiful Dublin, Ireland! November 19-20, 2025 | Dublin, Ireland Join us for an immersive 2-day event focused on leveraging and validating Artificial Intelligence (AI) to…

Details

Délégation Quebec

By Jadzia Famili November 7, 2025

Trouvez Aram Montazami, Mélanie Rose et Yara Massoud le 20 novembre à Paris.

A3P – Digitalization

By Jadzia Famili November 7, 2025

Join Parsa Famili, Niccolo Moreno and Angel Ruiz in Barcelona on Nov 18th This A3P conference will bring together industry experts from the pharmaceutical sector to explore the challenges and opportunities of digitalization. A full day dedicated to delving into the regulatory aspects of Annex 11, as well as in-depth sessions on alarm review, the…

Details

PDA West Coast Chapter – Quality Ball

By Jadzia Famili November 7, 2025

Join Parsa Famili and Whitney French at the Quality Ball in San Francisco Nov 7th Please join us for the PDA West Coast Chapter’s 2025 Quality Ball located at the California Academy of Sciences, a renowned research institute and natural history museum located in San Francisco’s Golden Gate Park. The event will be focusing on the critical intersection…

Details

Growth Day Direct – Daiichi-Sankyo & Rapid Micro Biosystems

By Jadzia Famili November 7, 2025

Join Sarah Alimirzaei at Growth Day Direct, Nov 12-13 in Munich, Germany. Many of the world’s leading pharma companies will showcase scientific presentations, guest speakers, and shared insights at this exclusive two-day event hosted by Daiichi Sankyo and Rapid Micro Biosystems. Reserve your seat today for our event taking place at the Munich Airport Marriott…

Details

Webinar: Risk-Based Quality Information Management

By Jadzia Famili October 9, 2025

Join us on October 22nd (7:00am – 9:00am EST) for an in-depth webinar focused on Risk-Based Quality Information Management. Corinne Cleary and Merle Eloise will speak on different issues companies face in Quality Information Management and they’ll discuss the exploration of various solutions to mitigate the risks involved. Click the link below to register: https://attendee.gotowebinar.com/register/5608412450938833502

Details