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Controlled documents, food safety plans, and environmental monitoring.
FSDOCS brings document control together with facility-specific Food Safety Plans and Environmental Monitoring Programs (EMP). Keep procedures, sampling records, laboratory findings, and review history connected to the work they support.
FSDOCS by FSCFY. Part of the FSCFY platform.
Connect the plan, the procedure, and the evidence.
Separate documents, plan worksheets, swab schedules, and laboratory reports make review harder. FSDOCS keeps these records organized by facility, with controlled revisions and human review.
Current friction
Manual approval trails
Scattered SOPs and forms
Difficult document retrieval
Weak connection between records and procedures
Key FSDOCS workflows.
Explore document control, Food Safety Plan preparation, environmental monitoring, and laboratory-review workflows.Documents, plans, and monitoring records
Controlled document library, ownership, and revision history
Document review and approval workflows
Facility-specific Food Safety Plan drafts and worksheets
Editable process-flow diagrams linked to plan revisions
EMP sampling-site register and controlled sampling plans
Swab collection records and sample history
Laboratory result entry, human review, and report evidence
Investigations and separate vector-sampling rounds
Result corrections with preserved versions and fresh review
Facility-scoped permissions and traceable activity
Food Safety Plans
Prepare facility-specific drafts with product and process context, working notes, structured hazard-analysis and preventive-control worksheets, and editable process-flow diagrams.Plan revisions preserve the reason for change and the related diagram. Draft preparation is not plan approval: qualified review, activation, and controlled issuance remain separate governed steps.
Environmental Monitoring Programs (EMP)
Organize registered sampling sites, required and randomized site selection, plan approval, collection records, and laboratory findings by facility.Sampling through follow-up
Sampling plans retain selection reasons and flag site shortages
Collection records connect sites, sample references, collectors, and times
Human laboratory review records criteria, decisions, and reasons
Investigations link findings to separate vector-swab rounds
Amended results retain originals and require fresh review
Routine-result PDF evidence is linked to the exact result version
An environmental finding does not automatically determine product release.
COA and laboratory review
Discuss review needs for routine EMP, vector follow-up, supplier certificates of analysis (COAs), and product-testing reports.Each report type retains its own criteria and authorized decisions. Final decisions remain with qualified people.
Platform connection
Document control should connect to food safety operations.
FSDOCS focuses on controlled documents within the FSCFY ecosystem, with facilities, users, permissions, audit logs, and reporting as its platform foundation.Product inquiry