Compliant and traceable knowledge, from GMP to pharmacovigilance
In pharmaceuticals, knowledge is a risk factor, because it must be correct, up to date and verifiable. Syllog keeps procedures, regulations and operational knowledge aligned in every regulated area, from production to medical-scientific information, with traceability ready for audits.
Trusted by
A single source of knowledge, always up to date
Procedures, SOPs and regulations in a single environment, aligned to the current version. Whoever works always accesses the most recent knowledge.
Every answer with the source, every access tracked
In a regulated sector, verifiability is an essential requirement. Every piece of content is linked to its source and every access stays on record.
Every function, serving Pharma
Quality, training, production and network: each function covers a different actor in the pharmaceutical process.
Syllog Compliance
Quality and regulatory keep the body of regulation in order, from GMP to pharmacovigilance all the way to data integrity obligations, and know at any moment who has read what.
Syllog HR
Anyone entering a regulated role is operational sooner, and at every procedure revision the people involved are requalified only on the part that changed.
Syllog Operations
People on the production line consult the correct SOP from the shop floor or at the machine, without searching through folders and without risking the wrong revision.
Syllog Marketing & Sales
Medical representatives use only approved materials in the current version, so the information that reaches the doctor stays within the permitted scope.
From regulation to ready-to-use knowledge
In any format, from GxP procedures to EMA, FDA and AIFA texts.
It turns it into paths, interactive video and audio, always up to date and ready to use.
The medical and regulatory team verifies before validating.
From the quality department to the network of medical representatives.
Frequently asked questions
Yes. The knowledge managed by Syllog is versioned, tracked and linked to sources: complete audit trail and access control, the standards required in GxP environments.
Every piece of content is linked to the document it comes from (papers, guidelines, SOPs, regulation) and the AI's answers always cite the source, so the team verifies before distributing the knowledge.
Yes. Syllog connects to the main pharma document management systems and LMS (Veeva Vault, Documentum, SCORM/xAPI standard) to import existing knowledge and distribute it where teams already work.
They stay isolated and reserved for company use only, with a contractual guarantee of exclusion from the training of third-party models. Encryption in transit and at rest, granular access and deployment options designed for pharmaceuticals.
Always your teams. Syllog proposes and organizes, but medical and regulatory remain the only ones to validate knowledge before it becomes public.
About two weeks for a first pilot scope, depending on sources and integrations. The Syllog team supports the setup and the import of content.
