MFLRC
Licensing and regulatory updates from our consultants.
June 14, 2026 · Regulatory Affairs
Canadian producers supplied 53 percent of Germany medical cannabis imports in Q1 2026. This 2026 roadmap maps the EU-GMP and GACP certification path Canadian LPs need to reach the German pharmacy channel, from gap analysis to overseas inspection.
#Cannabis
By Mussarat Fatima
June 13, 2026 · Regulatory Affairs
State-licensed U.S. medical marijuana operators must file for DEA registration by June 22, 2026 to keep operating, and the expedited Schedule III hearing runs June 29 to July 15. Here is what it means for U.S. operators and Canadian LPs.
#Controlled Substances
By Mussarat Fatima
June 13, 2026 · Natural Health Products
Health Canada's GUI-0158 Version 4.0 came into force March 4, 2026. A compliance checklist, QAP responsibility matrix, and FAQ for Canadian NHP licence holders and importers.
#GUI-0158
By Mussarat Fatima
June 12, 2026 · Regulatory Affairs
ICH E6(R3) Annex 2 was adopted at Step 4 on 3 June 2026, completing the modern GCP framework. Here is how Canadian sponsors and sites can get decentralized trial and real-world data compliance ready before Health Canada's 1 October 2026 deadline.
#Health Canada
By Mussarat Fatima
June 12, 2026 · Regulatory Affairs
Health Canada's new terms and conditions framework takes effect April 1, 2027, replacing the NOC/c pathway. A practical guide to agile licensing and lifecycle obligations for sponsors.
#Health Canada
By Mussarat Fatima
June 11, 2026 · Regulatory Affairs
Health Canada's April 2026 pre-market guidance for machine learning-enabled medical devices introduces the Predetermined Change Control Plan (PCCP). Here is what Canadian manufacturers need to know about data quality, bias management and licensing.
#Health Canada
By Mussarat Fatima
June 11, 2026 · Regulatory Affairs
The biggest rewrite of EU GMP Annex 11 since 2011 lands mid-2026: 17 chapters covering validation, audit trails, supplier oversight, cybersecurity and a new Annex 22 on AI. Here is the gap assessment roadmap for Canadian exporters to the EU.
#Compliance
By Mussarat Fatima
June 10, 2026 · Regulatory Affairs
The revised EU-GMP Chapter 4 is format-neutral: photos, video and real-time feeds now count as GMP records. Learn what data-integrity controls your site needs before mid-2026.
#Pharmaceuticals
By Mussarat Fatima
June 9, 2026 · Regulatory Affairs
The FDA's 2026 CDER agenda adds guidance on distributed manufacturing, AI/ML quality, PET drug CGMP, and Form 483 responses. Here is what Canadian exporters should do now.
#Pharmaceuticals
By Mussarat Fatima
June 8, 2026 · Regulatory Affairs
How psychedelic-assisted therapy is regulated in Canada in 2025: the three legal pathways (clinical trials, the Special Access Program, and Section 56 exemptions), the controlled-substance rules for psilocybin and MDMA, and what the Toth v. Canada Federal Court ruling means for practitioner training.
#Health Canada
By Mussarat Fatima
June 7, 2026 · Regulations
Health Canada is consulting on major reforms to the Industrial Hemp Regulations, including possibly dropping licence requirements for some activities. Comments close June 30, 2026. Here is what is proposed, who benefits, and how to write a submission that gets read.
#Cannabis
By Mussarat Fatima
June 5, 2026 · Regulatory Affairs
From April 2026, Canadian cosmetics can no longer hide key fragrance allergens behind the word "parfum." A practical roadmap: what changed, how to read supplier allergen certificates, updating labels and CNFs, and what the 2026 Hotlist proposals mean for your formulas.
#Health Canada
By Mussarat Fatima
June 3, 2026 · Regulatory Affairs
By 2026, EU GMP Annex 1 is fully in force and firmly enforced. Any Canadian pharmaceutical manufacturer or cannabis Licensed Producer exporting sterile or EU-GMP product to the EU or UK must have a documented, living Contamination Control Strategy (CCS) ready for inspection—or risk critical findings and loss of market access.
#Health Canada
By Mussarat Fatima
June 2, 2026 · Regulations
Cannabis excise tax reform in Canada is gaining momentum. The Expert Panel's final report urged a review of the $1/gram excise floor and potency-based duties, a 2025 Deloitte report sharpened the case, and micro-class limits have already quadrupled. Here's what could change for licensed producers and how to prepare.
#Cannabis
By Mussarat Fatima
June 1, 2026 · Regulatory Affairs
ICH E6(R3) Good Clinical Practice has been in force in Canada since 1 April 2026, with the transition period closing 30 September 2026. A verified quality-by-design and risk-proportionality readiness plan for sponsors, CROs, and sites.
#Health Canada
By Mussarat Fatima
May 24, 2026 · Regulatory Affairs
Health Canada's April 2026 Final Notice (following its 14 August 2025 consultation Notice) clarifies how exosome, extracellular vesicle, and cell-conditioned media topical products are classified at the cosmetic-drug interface. Learn the three statutory considerations, MFLRC's six-trigger framework, the cosmetic/NHP/drug/biologic decision tree, and a reformulation checklist for skin-care, hair-care, and medi-aesthetic brands.
#Exosomes
By Mussarat Fatima
May 21, 2026 · Food and Beverages
As of January 1, 2026, Health Canada’s Front-of-Package (FOP) nutrition symbol is mandatory on prepackaged foods and beverages that are high in saturated fat, sugars, or sodium. Learn what the new rules require, who must comply, key exemptions, and how to complete a defensible FOP readiness assessment for your full SKU portfolio.
#FOP Nutrition Labelling
By Mussarat Fatima
May 20, 2026 · Natural Health Products
Health Canada's new NHP GMP Guide (GUI-0158, Version 4.0) came into force on March 4, 2026. It introduces real-time stability expectations, evidenced importer oversight, and a full quality-systems approach. Here is what Canadian NHP licence holders need to do now to stay inspection-ready.
#GUI-0158
By Mussarat Fatima
May 19, 2026 · Regulatory Affairs
A practical breakdown of SOR/2025-242 — Canada's new Controlled Substances Regulations. Monthly reporting, unified dealer licensing, October 1, 2026 deadline, and what manufacturers and dealers must do now.
#SOR/2025-242
By Mussarat Fatima
May 11, 2026 · Medical Device
EUDAMED is no longer optional. From 28 May 2026, the first four modules become mandatory for every economic operator selling devices into the EU. Here's the pre-flight checklist MDEL holders and EU manufacturers should already be running.
#EUDAMED
By Mussarat Fatima
May 8, 2026 · Compliance
The DEA's April 28 Schedule III order reshapes cross-border cannabis. Canadian LPs: here's what 280E elimination, M&A, and the June 27 deadline mean for your quality system — and your next capital raise.
#DEA, Schedule III, 280E, Canadian LP, Quality Systems, Cannabis M&A, Health Canada, GMP, Pharmaceutical Validation, Regulatory Affairs
By Mussarat Fatima
May 5, 2026 · Compliance
Learn how to comply with Health Canada’s 2026 cannabis sampling guidance, including storage, security, record-keeping, and provincial rules for retailer samples.
By Mussarat Fatima
March 29, 2026 · Regulations
Discover how new cannabis regulations in Canada simplify compliance for licence holders, boost competition, and enhance the market—find out more!
By Mussarat Fatima
March 29, 2026 · Compliance
Learn how cannabis licensing consultants can help Canadian cannabis businesses streamline compliance with expert knowledge, comprehensive SOPs, audits, tracking and reporting systems, and more. Get insights from industry experts and stay ahead of changing regulations.
By Mussarat Fatima
March 19, 2026 · Cannabis regulations, label, Quality assurance,
By Mussarat Fatima
October 3, 2025 · Compliance
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September 30, 2025 · Compliance
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September 19, 2025 · Compliance
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September 12, 2025 · Good Production Practices
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August 28, 2025 · Compliance
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August 25, 2025 · Compliance
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August 19, 2025 · Compliance
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August 16, 2025 · Compliance
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August 13, 2025 · Compliance
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August 12, 2025 · Compliance
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August 12, 2025 · Compliance
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August 12, 2025 · Compliance
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August 12, 2025 · Compliance
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August 1, 2025 · GMP
By Mussarat Fatima
September 25, 2024 · GMP
By Mussarat Fatima
July 2, 2024 · Cannabis regulations, label, Quality assurance,
By Mussarat Fatima
June 10, 2024 · Compliance
Unlock the secrets of superior cannabis production hygiene with our latest blog post. Dive into GMP's rigorous cleaning protocols for braided stainless-steel cables, guaranteeing unparalleled quality and safety in every cannabis product. Elevate your industry knowledge and stay ahead of the curve today!
By Mussarat Fatima
March 25, 2024 · Compliance
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December 19, 2023 · Compliance
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December 19, 2023 · Compliance
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December 8, 2023 · Compliance
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December 4, 2023 · Compliance
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November 27, 2023 · License
By Mussarat Fatima
October 17, 2023 · Cultivation
By Mussarat Fatima
May 1, 2023 · Cultivation
By Mussarat Fatima
April 5, 2023 · Cultivation
Integrated Pest Management (IPM) is a science-based, sustainable approach to controlling pests in cannabis cultivation. This guide covers setting action thresholds, monitoring and identifying pests, prevention, and biological, mechanical and chemical controls — plus how to maintain continuity of care from mother stock to harvest while staying compliant.
#Cannabis
By Mussarat Fatima
March 28, 2023 · License
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March 27, 2023 · Regulations
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March 23, 2023 · Compliance
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March 20, 2023 · Compliance
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March 14, 2023 · Good Production Practices
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March 8, 2023 · Compliance
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February 22, 2023 · Compliance
By Mussarat Fatima
October 5, 2022 · Good Production Practices
Avoid these common mistakes when conducting a root cause analysis to ensure your investigations are successful and corrective actions are effective.
By Mussarat Fatima
September 9, 2022 · Good Production Practices
By Mussarat Fatima
September 9, 2022 · Compliance
By Mussarat Fatima
September 9, 2022 · License
By Mussarat Fatima
September 8, 2022 · Compliance
By Mussarat Fatima
