You will get a food supplement or dietary supplement label review
Project details
Food supplement or dietary supplement label review against UK, EU or US requirements.
1 label can be reviewed against UK, EU or US under one review.
Label pdf will be annotated with comments and a supplementary word document provided to demonstrate how comments refer to the regulation.
1 label can be reviewed against UK, EU or US under one review.
Label pdf will be annotated with comments and a supplementary word document provided to demonstrate how comments refer to the regulation.
Project Type
LegalWhat's included
| Service Tiers |
Starter
$200
|
Standard
$375
|
Advanced
$500
|
|---|---|---|---|
| Delivery Time | 3 days | 4 days | 4 days |
Optional add-ons
You can add these on the next page.
Fast Delivery
+$300 - $750
5 reviews
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This project doesn't have any reviews.
KD
Ken D.
Apr 9, 2025
30 minute consultation
Bethany is highly experienced in regulatory compliance. Beyond this she also an stronger understanding of the business / commercial perspective that form the basis of many regulatory queries. I would highly recommend her and her agency
DA
Daniel A.
Oct 1, 2024
Probiotic Regulation Support
Great to work with
IZ
Irina Z.
Oct 1, 2024
EU Food Supplements Compliance Specialist Needed
The research conducted for our compliance project was completed very quickly and to a high standard. Bethany demonstrated great flexibility and maintained a high level of responsiveness throughout the process.
JM
Joe M.
Feb 17, 2024
Food Supplement Compliance
BE
Brandon E.
Sep 20, 2023
Global Regulatory Expertise Needed in the Vitamins and Nutritional Supplements Industry
About Bethany
Regulatory Affairs Expert
100%
Job Success
Shirley, United Kingdom - 6:19 pm local time
I started my career at Reckitt Benckiser gaining experience within the R&D industry for medicinal, medical device and general products, before taking my first steps in my regulatory career within the Market Expansion team. During my time in the Market Expansion team I successfully led the DCP for Nurofen and headed up the Durex Market Expansion deliverables to expand the sales into new European markets and the rest of the World.
In 2019, following my time in the Market Expanison team I moved into the Durex Regulatory Category team to gain experience in technical file generation and new product development.
In 2020, I started my career at DePuy Synthes providing consultancy work for Russian registerations on their medical device products. This was a short term project to come into the business, remediate their technical files and ensure they are compliant to the Russian regulations and then support through the question stage between DePuy Synthes and the Health Authority.
In 2021, I moved into management at PDI Ltd leading the regulatory department for both the UK and Italy site, delivery registrations for medical devices, biocides and cosmetics and initiating a new project to regulate a product under the medicinal regulations, and successfully submited the MDR files to the notified body and delivered the Brexit Transition.
I am now heading up Global Regulatory Affairs at De Faire Medical who are a Swedish Biotech company with patented bacteria technology, where our vision is to deliver ground-breaking products to address some of the worlds largest consumer unmet needs.
I am available for Regulatory consulting and support within general products, cosmetics, food supplements, biocides and medical devices (MDD and MDR).
Steps for completing your project
After purchasing the project, send requirements so Bethany can start the project.
Delivery time starts when Bethany receives requirements from you.
Bethany works on your project following the steps below.
Revisions may occur after the delivery date.
Label review
- Product label pdf edited with comment for amendments - Checklist document referring to comments in the pdf label so client can see the requirements and what needs changing
1 round of review
- 1 round of reviews based on the comments provided at the initial assessment