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Stay ahead of the game with the latest EU cybersecurity requirements for manufacturing. Learn how to navigate the NIS2 Directive and ensure compliance with our white paper.
Learn from TIA Portal expert Michael Grollmus how to enhance production reliability with efficient data management, version control, and automated backups for Siemens TIA Portal.
Experience a new standard of compliance and efficiency in pharmaceutical production with octoplant version control software. Minimize compliance risks and backup automated processes so you can focus on delivering safe and effective life science products to market.
Pharmaceutical and life science manufacturers must comply with a range of regulations and standards. This requires full and detailed documentation of the entire production process and regularly conducted self-inspections. Every step of the manufacturing process must be documented to provide full records and complete traceability.
octoplant helps companies adhere to FDA and GxP rules with regard to process quality, production documentation and proof of compliance by backing up automated tasks and documenting all aspects of a production process.
Accurately track all production process changes, providing detailed insight into who, what, when and where changes were made.
Verify compliance with quality standards, including FDA (21 CFR Part 11) and GxP requirements.
Ensure early error detection and quality assurance by using the four-eye principle within the approval process.
Explore all the features of octoplant in the brochure.
By introducing the AMDT solution, we are minimizing the risk of PLC-failures that affect the quality of the medicines. This data management and change-software enables us resolve production stop issues and resume production as quickly as possible.
Yichang Humanwell Information Center
octoplant by AUVESY-MDT automates documentation processes, ensuring meticulous adherence to FDA and GxP regulations. By optimizing workflows and maintaining comprehensive audit trails, octoplant minimizes errors and enhances operational efficiency so you can focus on delivering safe and effective pharmaceutical products.
octoplant backs up automated documentation processes, ensuring adherence to FDA and GxP regulations with meticulous traceability throughout the production lifecycle.
octoplant’s automatic backups ensure you are able to quickly recover your production line configurations in the event of an interruption – minimizing downtime and ensuring continuity of operations.
Meticulously track and record every action and change in your processes, providing transparent and verifiable documentation. By automating audit trail generation, octoplant simplifies regulatory audits, ensuring you meet and exceed compliance requirements with ease.
octoplant supports more devices than anyone else in the industry, including PLCs (e.g. TIA Portal), SCADA systems, HMIs and robots from different manufacturers. This helps you better analyze the shop floor, isolate errors and fix any problems. See for yourself!
Data integrity can be ensured by implementing robust data management systems that track and document every change in the production process, maintain secure records and ensure that all data is accurate, traceable and compliant with regulatory standards.
Maintaining detailed documentation is crucial for regulatory compliance, quality assurance and traceability. It ensures that every step of the manufacturing process is recorded, making it easier to conduct audits, identify issues and validate product quality.
Automated systems can streamline production processes, reduce the risk of human error, enhance efficiency and ensure consistent compliance with regulatory requirements. They also simplify documentation and backup processes, improving overall operational effectiveness.
octoplant is an advanced version control and data management platform designed for the pharmaceutical and life sciences industries. It automates documentation processes, maintains comprehensive change histories and ensures regulatory compliance, thereby streamlining operations and enhancing efficiency.
octoplant automates the creation of detailed audit trails, tracking every change and ensuring all documentation meets stringent FDA and GxP regulatory standards. This simplifies regulatory audits and helps companies maintain continuous compliance.
Yes, octoplant minimizes downtime by automating backups and providing quick recovery options in case of emergencies. This ensures production continuity and efficiency, crucial in pharmaceutical manufacturing.
Yes, octoplant is designed to manage complex pharmaceutical production workflows by automating repetitive tasks, optimizing processes and maintaining detailed documentation, thereby improving overall efficiency and compliance.
Yes, octoplant is scalable and can be tailored to meet the needs of various operation sizes, from small laboratories to large pharmaceutical manufacturing facilities, ensuring flexibility and adaptability.
Navigate new EU cybersecurity standards with fines of up to €10 million. Which sectors are affected? Download our white paper for insights into the NIS2 Directive.
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