Pharmaceutical Track And Trace by VISIOTT's Solutions

You can implement serialization and aggregation operations using VISIOTT’s Pharmaceutical Track and Trace solutions. We develop our solutions for the pharmaceutical industry in two main segments: hardware and software. We also have documentation and project consulting services that complement these solutions. 

We can successfully manage integrations with government pharma traceability systems (DSCSA, EU-FMD, ITS, ANVISA, CRPT, etc), and other 3rd party software (SAP AATP, ERP, Tracelink, etc). Our expert team performs validation documentation and implementation of all software and hardware comply with the GAMP 5 and 21 CFR PART 11 standards. While performing this, we consider the high-quality requirements of the pharmaceutical industry. More than 100 companies in Turkey have been using VISIOTT solutions since 2009. And also, pharmaceutical companies in the international market have started to use our solutions with appreciation.

VISIOTT has developed its solutions in compliance with the regulations of the all countries with its experience in Turkey. Using our software and hardware solutions, you can easily perform serialization, aggregation, and notification operations complying with the regulations of these countries. VISIOTT is one of the rare companies that has achieved serialization and aggregation of over ten billion products worldwide. Our team considers patient safety and tries to provide the best solutions to our customers. We aim to maintain customer satisfaction at the highest level in the pharma track and trace requirements.

Our Software Solutions

We have developed our software taking into account all track and trace requirements of the pharmaceutical industry. Our improved line (L2), plant (L3), and company (L4) level software offers solutions following the regulations of US (DSCSA), Europe (EU-FM), Turkey (İTS), Russia (CRPT), Brazil (ANVISA), and other countries and makes the required notifications.

Our software solutions developed following the ANSI ISA 95 standards. Thus, you can achieve maximum data integrity and efficiency using minimum hardware resources with them. Our software is integrated into more than 50 ERP, MES, and Level 4 systems, already popular in the pharmaceutical industry. It can easily be integrated into other systems thanks to its customizable structure. You can get information about our line and plant level Pharmaceutical Track and Trace software clicking the pictures below.

Pharmaceutical Track And Trace Line Manager
Pharmaceutical Track And Trace l3_Plant_Manager

Pharmaceutical Track and Trace Focused Hardware

We design and manufacture all of VISIOTT’s machines in our manufacturing plant. Using our machines, you can easily implement serialization and aggregation operations in your high-speed pharmaceutical production lines. In addition, you can comply with the requirements of the EU-FMD regulations with our tamper-evident labeling stations. Our machine solutions work integrated with line (L2) and plant (L3) level software of VISIOTT. 

VISIOTT designs and produces serialization and aggregation stations compatible with all kinds of rarely used packaging in the industry, including cartons and bottles. We also manufacture low-function systems such as conveyors, turntables, and stainless tables. Also, we apply equipment cleaning and safety rules meticulously to all our designs and productions following GMP.

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Automatic Bundle Aggregation Station
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Manual Aggregation Station
Pharmaceutical Track And Trace
Semi-Automatic Aggregation Station
Serialzation Integration Solution For Cartoner
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carton_serialization_with_tamper_txt
Manual Aggregation Station
Semi-Automatic Aggregation Station
Automatic Bundle Aggregation Station
Swith Aggregation Station txt
Serialzation Integration Solution For Cartoner
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bls-100
Pharmaceutical Track And Trace
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Service, Maintenance and Support Services

Production downtimes are experienced in production lines since Pharmaceutical Track and Trace stations and software are new concepts. We offer 7/24 support, maintenance, and service agreements to minimize the production downtimes and maintain the OEE value. We classify your requests with our ticket-based employee support system and try to offer permanent solutions by a proactive approach. You can create a service request by sending an email to support@visiott.com. Our expert team will answer you as soon as possible.

Validation and Documentation

Our quality team and technical experts prepare validation documents of our GMP rules following GAMP 5 and related standards. Our company guarantees to manage all of its processes in compliance with ISO 9001 and ISO 27001 quality standards.

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