Regulator reporting
Build the culture record behind your regulatory reports
Connect source plants, culture history and observations in xPlant Pro. See what reporting systems ask for and how those records can support your team's preparation and review.
Put your culture records to work at reporting time
xPlant Pro connects cultures to their source plants, transfers, media recipes, SOPs and observations. Your team can return to that history when checking what happened and which records belong with a report.
For labs with Regulator Reporting enabled and a supported setup, xPlant Pro prepares reporting files or supporting documents from recorded lab data. The preview shows prepared information alongside its source records and identifies data that cannot be derived, so your team can review the output before downloading it.
Regulator Reporting is a separate add-on for eligible lab plans. Availability and setup depend on the reporting format your lab needs. Your team reviews the output and submits it through the required official route.
Generated outputs have not been verified as accepted by the named systems. The guide below describes official requirements; it is not a list of supported integrations.
Reporting systems and plant-health requirements
The records you need depend on your licence, the material you handle and where it moves. Explore the official reporting routes below.
Metrcparticipating US jurisdictions
Metrc records regulated cannabis activity for participating jurisdictions, including plant batches, growth stages and destruction. Immature-plant classifications, tagging rules and reporting obligations vary by jurisdiction. Use your regulator's rules when deciding how your lab's plants must be recorded.
Read official guidanceCCRSWashington
Washington's Liquor and Cannabis Board publishes CSV specifications for CCRS reporting, covering categories such as strains, areas, plants, inventory and adjustments. The records and files your business must submit depend on its licensed activity. Follow the LCB's current templates and submission guidance.
Read official guidanceCTLSCanada
Health Canada requires applicable federal cannabis licence holders to submit monthly reports by the 15th of the following month. Reporting includes opening and closing inventory, additions and reductions, and applicable sales information. The fields you complete depend on your licence and activities.
Read official guidanceTrack & Tracethe Dutch closed-chain experiment
The Netherlands' closed-chain cannabis experiment uses Track & Trace to follow material through its regulated supply chain. Designated participants record production and movements under the experiment's requirements. This scheme applies to its participants, rather than to every Dutch tissue culture lab.
Read official guidanceOffice of Medicinal CannabisNetherlands
The Office of Medicinal Cannabis, also known as BMC, handles cannabis-related Opium Act exemptions and has a defined role in cannabis imports and exports. Your authorised activities and shipments determine which permissions and records are required. Follow the official exemption and trade procedures for your operation.
Read official guidancePlant passports and export certificationNetherlands and EU
Plant passports apply to specified plants and plant products moving within the EU. Exports outside the EU may need phytosanitary certification under the destination's requirements. Dutch operators should follow NVWA and their inspection service's guidance on registration, inspection, traceability and the appropriate documents.
Read official guidancePCITUnited States, plant exports
USDA APHIS uses PCIT to manage phytosanitary certificate applications, issuance and tracking. Exporters provide consignment information and follow the destination's plant-health requirements. A lab's culture records can inform preparation, while inspection and certification follow the official process.
Read official guidanceSAHPRASouth Africa, medicinal cannabis
SAHPRA's cultivation guidance describes batch documentation and records of cultivation, production, stock and movements for medicinal and research cannabis activities. Your licence conditions determine the evidence and reporting your operation must maintain. Culture history is one part of that wider documentation.
Read official guidanceeCertSouth Africa, plant exports
South Africa's eCertification service provides an online route for phytosanitary applications and status tracking. Exporters submit the required information for review by the plant-health authority. Keep the consignment details and supporting records consistent with the application.
Read official guidanceODC reportingAustralia
Australia's Office of Drug Control requires relevant medicinal cannabis permit holders to report cultivation and production or manufacturing activities through its reporting template. Reports are submitted quarterly with monthly breakdowns and cumulative calendar-year totals. Use the current template and guidance for each permitted site.
Read official guidanceDescriptions checked October 4, 2026 against the official sources linked above. Requirements and submission procedures can change; check the current guidance for your licence and activity.
Cannabis and hemp activities are restricted or prohibited in many jurisdictions. The cannabis reporting examples on this page concern authorised operations only. This guide is not legal advice; your lab remains responsible for its permissions and compliance.
Check CITES alongside plant-health requirements
Phytosanitary requirements and CITES address different questions. A shipment of listed plant material may need CITES documentation as well as plant-health documents, depending on the species, material and applicable exceptions. In the United States, FWS and USDA APHIS have distinct roles, and requirements from both may apply.
xPlant Pro helps you follow a culture back to its source plant and review its recorded history. That context can support your team's document preparation; the relevant authorities determine which permissions and certificates are required.
Need another reporting route?
Tell us which authority your lab reports to and share its official requirements or template. We can discuss how your records relate to the reporting format and confirm the current scope of Regulator Reporting for your lab.
Questions before you choose
Does xPlant Pro submit reports to my regulator?
No. For supported setups, Regulator Reporting prepares files or supporting documents for your team to review and download. Your team submits them through the required official route. xPlant Pro does not issue permits or certificates, or guarantee that an output will be accepted.
Which requirements apply to a tissue culture lab?
They depend on your jurisdiction, licensed activities, species, material and destination. Cannabis reporting, plant passports, phytosanitary certification and CITES can involve different authorities. Tissue culture does not automatically place every plant under the same batch or tagging rule.
What if my regulator is not listed?
Share the authority's name and official reporting requirements when asking about Regulator Reporting. We can confirm the current scope for your lab. Inclusion in this guide describes a reporting route; it does not mean every requirement or submission format is supported in xPlant Pro.
Does using xPlant Pro make my lab compliant?
xPlant Pro supports record keeping and reporting preparation. Your lab remains responsible for its licence conditions, required evidence and submissions. The benefit is a connected culture history your team can review when preparing that work.
Make your culture records easier to review
Bring source plants, culture history and observations together in xPlant Pro. Start for free with a plant and an explant record, then choose the plan that fits your lab.
Regulatory information checked against the linked official sources on October 4, 2026. This is an independent guide; no approval or endorsement by the named authorities or system providers is claimed.