Cleanroom GMP tablet supplier AGL partners with new software firm

Published: 24-Jan-2024
Regulatory Digital Pharmaceutical

AGL Automation has partnered with Novatek Europe to offer their cleanroom software range for use on the range of cleanroom GMP tablets for paperless cleanrooms

AGL Automation, an automation solutions company that supplies cleanroom tablets, has partnered with Novatek Europe.

Novatek is a regulatory-compliant software solutions company that has offered its cleanroom software range for use on the range of cleanroom GMP tablets.

With AGL's GMP A certification, the CT range of tablets is perfect for use with Novatek Europe's software solutions. For example to run Novatek Europe's cleaning validation software or to assist with going paperless in the cleanroom.

Novatek Europe specialises in software innovation for the pharmaceutical, biotech, and healthcare sector

Novatek Europe specialises in software innovation for the pharmaceutical, biotech, and healthcare sectors.

In particular, the company specialises in transforming how environmental monitoring, stability studies, and cleaning validation processes are managed, ensuring they align with the latest regulatory standards.

  • Companies:
  • Novatek International
  • AGL Automation
See more

You may also like

Regulatory

Novatek requalifies as Boehringer Ingelheim approved supplier

Read more
The company’s products are designed to assist in managing critical aspects of a quality-controlled environment

Trending Articles

  1. What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
  2. Combustible dust in pharma: An elusive but very real risk Controlling contamination and controlling hazards simultaneously in today's cleanrooms is difficult, sometimes even oppositional. Many operations have serious gaps that are difficult to reconcile without the proper expertise. J.T. Cochran from CRB Group discusses
  3. Nortek Air Solutions CleanSpace relaunches SERVICOR for modular cleanrooms Nortek Air Solutions CleanSpace shared with Cleanroom Technology how SERVICOR for modular cleanrooms, complies with ANNEX 1 requirements, as it was relaunched to meet industry demands for cleanrooms that can achieve the required filtration levels
  4. GMP Annex 1: Validation of disinfectants on cleanroom surfaces Published in August 2022, for implementation in August 2023, Karen Rossington from Contec looks at the revised version of EU GMP Annex 1 expanded and clarified the regulatory requirements of cleaning and disinfection in life science cleanrooms
  5. The importance of growth promotion testing Given the critical nature of microbiological quality tests which are employed to ensure that pharmaceutical products are safe for human use, it is in turn essential to undertake quality control (QC) tests to ensure that the culture media being used for these is fit for purpose and performs properly. Cherwell Laboratories' Steven Brimble explains

Upcoming event

Pharmig Annual Pharmaceutical Microbiology Conference

20–21 November 2024 | Conference | Nottingham, UK See all

You may also like

Regulatory

Novatek requalifies as Boehringer Ingelheim approved supplier

The company’s products are designed to assist in managing critical aspects of a quality-controlled environment
Analysis

Novatek to work on automating EM program for Boehringer Ingelheim

The research-driven pharmaceutical company has decided to go with a dedicated solution for its environmental monitoring needs
Digital

Xplore and Novatek to provide tablet PC for cleanrooms

The Novatek EM-Mobile solution reduces time in the pharmaceutical environmental monitoring process
HVAC

Nortek Air Solutions CleanSpace relaunches SERVICOR for modular cleanrooms

Nortek Air Solutions CleanSpace shared with Cleanroom Technology how SERVICOR for modular cleanrooms, complies with ANNEX 1 requirements, as it was relaunched to meet industry demands for cleanrooms that can achieve the required filtration levels
Design & Build

Bonalive Biomaterials expands production capabilities

The medical technology company has moved its headquarters to a new building with increased production capabilities. The construction and renovation of the new building is in the cleanroom validation stage
Pharmaceutical

Braunform launches 32-cavity production mold for insulin pen housings

The injection molds and plastics technology specialist has launched a 32-cavity production mold for insulin pen housings
Design & Build

EXCLUSIVE: Case study: C-CUBE's first biotech modular project in Europe

Christophe Mermaz, Co-Founder and CEO of C-CUBE shared with Cleanroom Technology the process and methodology behind building its first biotech modular project in Europe
Subscribe now