Increase quality and control
Pharmaceutical and life science manufacturers must comply with a range of regulations and standards, such as FDA and GxP. This requires full and detailed documentation of the entire production process and of regularly conducted self-inspections. Each manufacturing step, every organisational measure and all process conditions must be documented end-to-end to provide full records and complete traceability. octoplant help companies adhere to FDA and GxP rules with regard to process quality, production documentation and proof of compliance.
octoplant's comprehensive change history allows you to accurately track all production process changes, providing detailed insight into who, what, when and where changes were made.
octoplant facilitates thorough verification of compliance with quality standards, including FDA (21 CFR Part 11) and GxP requirements.
octoplant ensures early error detection and quality assurance by using the four-eye principle within the approval process.
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 hepls you better analyze the shop floor, isolate errors, and fix any problems. See for yourself!
Discover the impact of the EU NIS2 Directive on manufacturing companies! With penalties of up to €10 million or 2% of global turnover, stricter cybersecurity requirements are a reality for industries such as pharmaceuticals, chemicals, and more. Our free guide offers concrete solutions to ensure compliance and minimize cyber threats.
Download the free whitepaper now!