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Novatek International

Quebec, , Canada

Pharmaceuticals Products - Manufacturer, Services,
Pvt. Ltd. Firm Since 0

Novatek International has effectively secured its position as a technology leader and driving force in the changing dynamics of the life science marketplace. Novatek?s business is focused on the following markets: Pharmaceuticals, Biotech, Chemical, Biological, Contract labs and Medical Industries.

Since inception, the company's primary goal is to provide leading edge, flexible and user-friendly, laboratory information management technology. Hundreds of users demonstrate Advanced Quality Nova-LIMS? proven performance on a daily basis as Advanced Quality Nova-LIMS is installed in more than 200 analytical laboratories, quality inspection organizations and high-end clinical operations throughout the world. Novatek's customers include municipal and private laboratories, as well as Fortune 500 corporations in the chemical, clinical, food, environmental and pharmaceutical industries.

Developments within the LIMS industry are ever present and changing. Our staff is a highly qualified group with extensive experience in software development, multimedia, Internet applications, graphics and technical writing.

Our mission is to empower people through inspiring software. We are committed to fulfilling our clients? requirements at all times and therefore we continuously innovate using their suggestions and/or requests, to better serve their needs. We respect the highest ethical standards and strive for excellence in everything we do to produce products of the highest quality.

Selecting Advanced Quality Nova-LIMS secures your investment now and into the future.

To find out how your company can benefit from Novatek?s advanced quality products, you are invited to review the information on this site or contact Novatek International?s headquarters.

Products :
We provide leading edge, flexible and user-friendly, laboratory information management technology. Novatek?s business is focused on the following markets :- Pharmaceuticals, Biotech, Chemical, Biological, Contract labs and Medical Industries. Products :- Advanced Quality Nova-LIMS : Advanced Quality Nova-LIMS is a 21 CFR Part 11 Compliant long-term solution that ensures you have centralized control and maintenance of all your data handling software solutions. It is a client/server product comprised of specialized functional modules such as the Environmental Monitoring Module, the Stability Module, the Raw Material Analyzer, the Finished Product Analyzer, the Calibration and Preventive Maintenance Module, the Automated Packaging Component Analyzer and Document Management System, audit and training Module. It is modular, ensuring users only need to purchase the modules that concern the sample types they require. Further more, as the company grows and needs change, additional modules can be purchased and activated with a minimum of integration and validation. Advanced Quality Nova-LIMS is Microsoft compatible and interfacing with any office management or Instruments through Instrument connectivity software, is possible creating a complete and paperless integration of data. It contains comprehensive functionality that enables client specific customization and rapid implementation. Our professional staff guides you through implementation, validation and training. Advanced Quality Nova-LIMS represents an investment in a technological improvement to the current system of information management. Stability Program? Software Application :- The Stability module is a software application that manages the day-to-day activities of the stability department within the quality control and/or R&D divisions. Its design takes into consideration the latest guidelines from the FDA, TPP, ICH and EU, among others, pertaining to pharmaceutical, chemical, biological and biotechnological fields. This software is designed for all types of products, from pre-clinical to post market, innovator or generic. The Stability module is 21 CFR part 11 compliant and has an extensive, independent audit trail. Environmental Monitoring Program? Software Application :- Environmental Monitoring Program is an application capable of capturing all environmental data in a 21 CFR Part 11 Compliant, fully validated system. It is envisioned for sterile and non sterile health care industries (Pharmaceuticals, Biotech, Chemical, microbiological) food and any other sterile environment based on the latest guidelines from, FDA, EU, ISO 14644-1 and PDA Technical report 13. Data from viable and non viable monitoring, Water analysis, clean steam and compressed gases are securely captured and easily trended to ensure site "state of control". The investigation window allows the user to investigate Out of Specification "OOS" with capability to add any files such as picture, audio video, scanned documents etc to the report. D.A.T.A.? Document, Audit, and Training Software Application :- DATA is a 21 CFR Part 11 compliant application used to manage and exchange information in all industries. It is made of three distinct modules: a document management system, an audit module and a training module. DATA incorporates several customer-driven enhancements and innovations. The Finished Product Analyzer? Software Application :- The Finished Product Analyzer module is a software application that is used for capturing the test data from finished product testing. This application consists of Product Registration, where the user can input pertinent information regarding the product and the type of packaging; Monograph, where the user can define the required tests; Certificate of Analysis: used for entering, verifying and approving the data; The Approved manufacturers and Suppliers list; where the user verifies that the product is from an approved source; Investigation; where the user can initiate an Out of Specification Investigation. The trending of lots is possible to ensure that the process is under control. The Finished Product module is also 21 CFR part 11 compliant and has an extensive, independent audit trail. The Raw Material Analyzer? Software Application :- The Raw Material Analyzer module is a software application that is used to facilitate the testing of Raw materials and incoming Packaging components. The Software consists of the following windows: Product Registration, where the user can input pertinent information regarding the product and the type of packaging used in shipment of the Raw Materials; Monograph, where the user can define the required tests; Certificate of Analysis: used for entering, verifying and approving the data; The Approved manufacturers and Suppliers list; where the user can verify that the product is from an approved source; Investigation; where the user can initiate an Out of Specification Investigation. The trending of lots is possible to ensure that the raw material manufacturing process is under control. The Raw Material module is 21 CFR part 11 compliant and has an extensive, independent audit trail. The Preventive Maintenance and Calibration? Software Application :- The Preventive Maintenance and Calibration (PMC) module is a software application that is used to track the status of equipments used in a regulated environment. The software allows the registration of the equipment, the definition of the required tests to ensure the equipments are within the specifications and a test report where the user can enter the obtained results. The software will automatically show the equipments due for calibration. The inventory control window allows the purchase and update of the required spare parts for each calibration. The PMC module is also 21 CFR part 11 compliant and has an extensive, independent audit trail. The Automated Packaging Component Analyzer? Software Application :- The Automated Packaging Component Analyzer (APCA) module is an application used to automatically verify the incoming printed components against a pre-approved master. This software is language independent and capable of detecting the smallest error within the test and the master scans. It is capable of analyzing a predefined number of samples against the master and providing the error in each and every test sample. The user will have the choice to accept or reject the printed components based on the type of errors obtained. The APCA is envisioned to replace the tedious task of manually verifying a printed component against the master. The APCA module is, once again, 21 CFR part 11 compliant and has an extensive, independent audit trail. The Column Organizer? :- LC/GC Column Organizer is an essential software application for tracking and managing HPLC and GC columns in any laboratory environment. The LC/GC Column Organizer is 21 CFR Part 11 compliant and has an extensive, independent audit trail. The Column Organizer is provided with a LC/GC Column Cabinet, making it an integrated Software/Cabinet solution facilitating easy and efficient column management, thereby alleviating the time consuming task of searching drawers and boxes for misplaced columns. The Consumable Inventory Management System? :- Novatek?s Consumable Management Software (CMS) is a 21 CFR part 11 compliant, comprehensive inventory management system. It allows management of purchase orders, receivables, inventory locations, transfers, and serialized item tracking. Each material item in the price book has corresponding inventory details that can show all purchases, sales, quantities on hand, quantities reserved, quantities at each physical location, and the latest costs and values. The strength of the product lies in its non-modular design that enables you to enhance your business productivity significantly without ever having to add separate software. With Novatek?s CIMS, you get a powerful yet affordable 'mini-ERP' solution right-out-of-the-box! SleepVision? Software Application :- SleepVision is a program capable of capturing up to two video and audio streams independently. Patients with sleep disorders and other sleep related problems are filmed while asleep so that their physicians can view the video and prescribe a remedy. The main application of this software is in the sleeplab, where the monitoring of patients' movements is a tedious task. The Windows NTTM version of SleepVision TM is the property of Martinex Inc., and is distributed by NovaTek International.

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Contact Info

Novatek International

PO BOX 371
Mount-Royal
Quebec - H3P 3C6 () Canada

Phone(s) : 514-336-6809 / 788-6023
Mobile :
Fax : 514-336-6537


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