Value for Every Role in the Supply Chain
Pre-Verified Product Quality
Batches are independently audited against European pharmaceutical standards prior to export. Each shipment is supplied with certification issued by an accredited certification body confirming that the product meets the agreed specifications and regulatory requirements. This reduces the risk of fraud, non-conformities, and unexpected situations on arrival.
Reduced Regulatory Risk
Constant third-party oversight is applied across the supply chain, from cultivation through to dispatch. This strengthens the importer’s regulatory position, especially when operating from abroad, and reduces the likelihood of shipments being flagged during inspection, as the documentation is supported by an accredited, independent certification body.
Access to Qualified Suppliers
Producers are assessed against EU-GACP requirements and the Clear Certification Standard before entering the network. This helps importers work only with suppliers who have already demonstrated compliance, reducing onboarding risk and operational uncertainty.
Enhance Your Professional Standing
Presenting Clear (CCS) Quality Assurance Framework means introducing transactions that are undergoing real accredited batch-level verification. This reinforces buyer confidence, reduces objections during negotiation, and positions you as a credible and reliable market intermediary.
Lower Transaction Risk
Batches are reviewed and verified prior to export, helping to prevent border issues, documentation gaps, or disputes over quality. This results in fewer failed transactions and a more stable and predictable deal pipeline.
Engage with Serious Counterparties
This unique level of quality assurance brings structure and transparency to the transaction. Buyers and sellers operate within a documented, verifiable framework rather than relying on informal assurances, which supports faster alignment and progress toward contract.
Protect and Build Your Reputation
Each transaction contributes to your market perception. Working with independently verified batches reduces the risk of association with non-compliant suppliers and strengthens your profile as a broker who delivers secure, well-managed deals.
Accelerate Decision-Making
Because key compliance checks are addressed in advance, negotiations tend to move more quickly. Stakeholders require fewer clarifications, legal teams have clearer footing, and overall confidence in the transaction increases.
Independent Batch Verification
Each batch is reviewed by an accredited third party to confirm that lab results and product specifications match the delivered material. This adds an external layer of assurance beyond internal QA controls.
Audit-Ready Documentation
Every certified batch includes full third-party acquired traceability records and structured documentation from the source. This makes regulatory inspections easier to manage and provides clear evidence of compliance.
Lower Compliance Risk at Import/Export
Batch-level audits help prevent documentation gaps, product discrepancies, or flower grading issues during cross-border movement, reducing the likelihood of non-compliance findings or product rejection.
Operational Support for QA Teams
With verification and documentation support handled externally, internal QA resources can concentrate on day-to-day quality management rather than chasing paperwork or resolving disputes.
Reduced Border Delays
Shipments are accompanied by structured compliance documentation and batch verification, helping to minimise the risk of customs holds or clearance delays.
ISO-Certified Chain of Custody
Certified anti-tampering controls ensure the product remains traceable and tamper-evident from pickup to delivery, supporting compliance across jurisdictions.
Visibility Across the Journey
Batch tracking and handling records provide real-time oversight, so any irregularities can be identified and addressed immediately.
Strengthen Client Outcomes
Certification provides an independent validation of the systems you help your clients implement, turning your advisory work into a formally recognised compliance result.
Differentiate Your Practice
Being able to guide clients through an accredited certification pathway positions you as a higher-value advisor, not just a service provider.
Reduce Compliance Uncertainty
A structured framework aligned with GACP, GMP and GDP principles helps remove ambiguity and guesswork when preparing clients for regulated markets.
Objective Gap Identification
Independent assessments highlight what is missing in a client’s operation, giving you a clear, factual basis for defining improvement plans.
Support International Market Readiness
Clients gain stronger documentation, audit trails and process discipline, improving their ability to operate across multiple jurisdictions.
Long-Term Engagement Potential
Our QMS creates a natural lifecycle of continuous improvement, strengthening ongoing advisory relationships.
Buyer-ready credibility
independent verification supports faster qualification and fewer objections.
Fewer shipment disruptions
stronger pre-export checks reduce holds, rejections, and disputes.
Premium market positioning
documented transparency differentiates the operator from non-verified suppliers.
Less due-diligence friction
traceability and batch evidence are structured and defensible from day one.
Repeatable export readiness
standardised controls support consistent performance across batches and sites.
Public health protection
stronger assurance that only compliant product enters the regulated channel.
Centralised oversight
clearer visibility across licensed operators, batches, and movements, without relying on self-declarations.
Stronger enforcement capability
standardised, auditable evidence makes inspections and corrective actions faster and more defensible.
Lower diversion and integrity risk
documented chain-of-custody improves accountability across every handling point.
International credibility
accredited third-party verification strengthens confidence with foreign authorities and institutional buyers.
National competitiveness
a recognised compliance infrastructure positions the country as a trusted export origin and attracts higher-quality operators and investment.
Reduced political/regulatory exposure
fewer scandals and fewer “grey-zone” cases, because controls are measurable and traceable.
Why Clear?
We enable responsible operators to demonstrate their standards, and gives buyers and authorities confidence in every batch that crosses a border.
Globally Accredited Certification
CCS certification is issued in partnership with QS Quality Services Ltd., an ISO 17021-accredited certification body.
Clear Certification Standard (CCS)
Our chain-of-custody certification is purpose-built for the cannabis industry and provides independent verification of batch security and tamper integrity, operating under internationally recognised accreditation frameworks aligned with EA and IAF standards.
Independent Batch Auditing
Clear provides independent, third-party oversight in a sector often reliant on self-reporting. We conduct on-site batch audits and sealing prior to export under formal protocols, strengthening trust and reducing the risk of inspection issues or legal exposure for all parties.
Proven Industry Expertise
Clear’s team brings together ISO-certified auditing expertise and deep industry experience across cultivation and pharmaceutical manufacturing. We understand GACP, GMP, GDP and international narcotics regulations.
