Resources
Insights on GMP compliance, data integrity, and quality management for pharma, biotech, and healthcare teams.
We are looking forward to seeing our clients at our next User Group Meeting: Closing the Gap: A Holistic Contamination Control Strategy for Annex 1 Hosted by Novatek and Boehringer Ingelheim in Ingelheim, Germany on Monday October 30 to Tuesday October 31, 2023. Confirmed speakers and participants include: Contact your Novatek Rep. today to learn more…
Prevention. Deceleration. Reversal. These words were top of mind throughout the event. Funds raised support Hope for Dementia’s activities and programs that promote dementia prevention, aim to decelerate cognitive decline, and support promising research on the reversal of the symptoms of dementia. The impressive lineup of speakers from the public, private and scientific sectors endorsed…
We are partnering with MilliporeSigma to support the pharmaceutical industry in transferring their microbiological workflows into computerized systems to improve data integrity. Aligning our compliant software solutions with MilliporeSigma’s reliable and validated hardware and consumables will allow the pharmaceutical industry to work with the best from both expert suppliers in all parts of the same…
There are many books that cover Good Manufacturing Practices, however this latest publication on Analytical Testing for the Pharmaceutical GMP Laboratory by WILEY Publishers is by far one of the most concise and comprehensive to date. Editor Kim Huynh-Ba has gone above and beyond to consolidate a good mix of industry regulation, guidelines, and procedures all in one text…
Leading pharmaceutical company Remedica chooses Nova-LIMS for use at their multiple large scale manufacturing facilities in Cyprus. Novatek is proud to be part of Remedica’s Quality initiatives which are based on using specialized and advanced electronic monitoring instrumentation and systems to impose strict controls on all stages of the production process, from the authentication of…
How multifaceted, risk-based solutions maximize efficiency, speed, and quality Author: Susan Cleary, Director of Product Development The consequences of contamination in pharmaceutical manufacturing go far beyond compromising patient and consumer safety. Lost revenue due to slowdowns and contaminated supplies, fines from regulatory entities such as the U.S. Food and Drug Administration, and reputational damage are…
Novatek is proud to onboard BioGeneric Pharma as a full quality software portfolio client. BioGeneric Pharma holds high standards in adopting as much automation where they can at their 4000 m2 production site in Cairo, Egypt. With a full investment of Novatek’s software modules in Contamination Control, LIMS, and Quality Management Systems (Nova-QMS) including Calibration…
FULL PRESS RELEASE HERE: Read the English Newswire press release MONTREAL, Dec. 16, 2021 /CNW/ – On Friday December 3rd, 2021 Novatek International and it’s charity arm, Hope for Dementia was awarded as a community leader within the entire Laurentian Region of Quebec with a Corporate Citizen Trophy. Hosted via virtual ceremony, by both the Chambre de commerce et d’industrie de Saint-Laurent – Mont Royal and Centre…
We’re honored to have Novatek’s Asia Director to be featured in ISPE’s Pharmaceutical Engineering Magazine this month. You can read Vivien’s full article on Adapting Technology & a Culture towards Emerging Technologies in the link below! Great work Vivien! Read Vivien’s article here! About the Author: Vivien Santillan is Regional Director for Asia, Novatek International,…