Postbiotics: What Are They and How Do They Fit Into the Health Product Industry
Common Stability Testing Questions for Natural Health Products (Canada) and Dietary Supplements (U.S.)
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Oh Cannabis: Navigating the New Regulations for Cannabis Edibles in Canada
The Continued Rise of Probiotics: A Q&A With George Paraskevakos
Team Talk: Meet Rob Greco, Clinical Trial Coordinator
Top 3 Reasons to Conduct Clinical Research in Canada
The 3 Requirements for Selling a Natural Health Product in Canada
A Regulatory Recipe for Adding Prebiotics and Novel Strains to Your Probiotic Line
Seeing Clearly: Using Transparency to Regain Trust in the Supplement Industry
Your (Canadian) CBD Questions Answered
Go to Market in Multiple Countries with One Product Spec
GRAS for Grass: Is Generally Recognized as Safe a Viable Pathway for CBD Market Access?
Team Talk: Meet Katie Keene, Clinical Research Coordinator
Ready to Comply with New Supplement and Nutrition Labels by 2022?
The Supplement Industry Still Has a Claims Substantiation Problem. Here's How to Fix It
GRAS or NDIN: Which is the Right Regulatory Strategy for My Ingredient?
Regulatory Trends That Will Shape 2019
Shotgun Metagenomics: A Viable Solution for Species Identification of Supplements and Foods?
Supplement and Weight Loss Strategies to Help Active Consumers Stay Lean and Fit
How to Form a CRO Partnership That Delivers Results
How to Not Get Kicked Off Amazon.ca for Non-Compliant Natural Health Products
Prop 65 Updates: How to Ensure Dietary Supplement Compliance in California
Substantiating Products With No Guidance: The CBD Confusion
Implications of FDA's GRAS and NDIN Policy Changes for Supplements and Medical Foods
Next Steps for Commercializing Medical Cannabis Products in Canada, the U.S., and Beyond
Reverse-Engineering Your Regulatory Strategy for More Efficient Product Development
How Health Canada’s Upcoming Self-Care Product Regulations Could Impact Your Marketed Natural Health Products, Non-Prescription Drugs, and Cosmetics
Can DNA Testing Solve the Supplement Industry’s Identity Problems?
What to Expect When Conducting Dietary Supplement Clinical Trials
Nutrasource, GOED, DSM Jointly Publish Largest-Ever Fish Oil Oxidation Study
Let's Connect at 2018's Most Buzzworthy Natural Health Events
Understanding the Clinical Trials Pathway for Probiotics
The Future of Probiotics from the International Probiotics Association
Planning for Risk Mitigation Is Key to a Successful Clinical Research Strategy
Managing Risk in Probiotic Stability
Setting Higher Quality Standards for Label Claims
Demystifying Clinical Study Designs for Probiotics
The Future of Probiotics is Bright: Q&A with International Probiotics Association's George Paraskevakos
What to Look for in a Dietary Supplement CRO
5 Essential Tips for Substantiating Dietary Supplement Claims
Taking an Integrated Clinical and Regulatory Approach for the Prebiotic/Probiotic Market
Understanding the Differences Between Phase I, II, III, and IV Clinical Trials
Start with the Product Claim When Developing a Dietary Supplement
Is Your Dietary Supplement Commercialization Plan on Target?
The 5 Key Questions to Ask Before Your Next Product Launch
Benefits of Conducting Clinical Research in Canada
An Introduction to Generally Recognized as Safe (GRAS) Filings for Food Ingredients
Health Claims That Can Get You in Hot Water
Your Top Regulatory, R&D, and Testing Questions Answered
Can Your Dietary Supplement Claims Stand Up to the FTC?
How to Choose an Analytical Testing Lab for Dietary Supplements
Top 10 Stability Storage and Testing FAQs
The Value of Third-Party Certifications for the Natural Health Industry
5 Questions to Ask When Navigating the Regulatory Pathway
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