Join us at IVT’s 7th Annual Labweek this December! An event, which has been known to consistently provide excellent direction and advice that attendees can use and apply within their own organization! We are especially excited to be collaborating on a very high-demand topic Wednesday Dec. 4th @ 3:30PM: Paperless Lab, Electronic Lab Notes (ELN)…
Join Novatek at CBI’s 2nd Annual Compounding Pharmacy Compliance where Novatek will provide tips and insights on achieving quality control and compliance for compounding facilities. Environmental Monitoring (EM) for compounding facility’s operations is very valuable. By implementing a dedicated and compliant environmental monitoring system within an existing QC Microbiology program substantially minimizes the risk of contamination…
KENX’s GMP University Event this Summer will surely be one not to miss! Three co events will be happening in one location focused on the following areas: Change Control Quality Risk Management Internal Audits and FDA Inspections Novatek will be both speaking and sponsoring this event!
Novatek is proud to sponsor this year’s East Coast Event! The pharmaceutical microbiology industry has seen many changes during the progression into the 21st century. With advances in rapid microbiological methods, revisions being made to regulations in the industry, enhanced knowledge of the human microbiome, and novel testing methods, this industry is ever expanding. Join…
Data Integrity • Method Transfers and Validation • Stability Testing Novatek will be presenting and exhibiting at this year’s IVT Lab Week! Contact us if you would like to book a one on one session on site on how automated Stability Study Management can help create more compliance and efficiency in your labs! Lab Week…
Paving the Way to Validation Excellence! Novatek will be sponsoring IVT’s 24th Annual Validation Week in San Diego, CA this year. Convening validation professionals of all levels for unmatched training, IVT’s 24th Annual Validation Week provides a transformative exploration through the world of validation. Build your own conference adventure and trek your way between four unique tracks…
Over three full days hear from FDA, MHRA, and pharmaceutical industry experts as they set the framework for discussion on basic quality systems as well as the influence of ICH Q10 on the industry as a whole. As companies continue to address issues such as data integrity, the quality systems platform of ICH Q10 becomes…
MARK YOUR CALENDAR for IPA’s 2018 Annual GMP Update | BPF Mise à jour Conference! International Pharmaceutical Academy (IPA) is delighted to be hosting its 14th annual GMP Update | BPF Mise à jour 2018 on October 3-4, 2018 in the historical city of Montreal, Canada. The conference will provide attendees with insight and a…
Come see us at Booth 37 in Washington DC for the 2018 PDA/FDA Joint Regulatory Conference! The PDA/FDA Joint Regulatory Conference is now in its 27th year. This important conference provides a forum for discussions centered on the requirements that assure the availability and delivery of high-quality medical products, and offers an opportunity to hear about the…
Cleaning Validation Summit 2018 Cleaning Standards For Drugs and Devices From Industry Experts Are you up to speed on the new Science, Risk and Statistics based approaches for Cleaning Validation? Today’s regulators are now asking for, and expecting, ADE Monographs and Risk Assessments of Cleaning Validation Programs. This two-day intensive summit brings together industry leaders…