current affairs
Issue 263, 3rd October – 4th November 2025
Training news
Complementary medicines and medical devices
Foods
Cosmetics and sunscreens
ACCC and other news
Training news
Regulatory Training Direct is an online training organisation with a focus on regulatory compliance and related topics.
Our course Compliance Obligations for Listed Complementary Medicines was developed specifically for startups and overseas companies with dietary or food supplements wanting to export their products to Australia, where most would be classified as complementary medicines. There is a lot you need to know about before you commit to launching in Australia! This course teaches you key compliance obligations. The course agenda is available here. This course was previously only available live via a Zoom appointment; but due to time zone differences which often don’t suit companies outside of Australia, we have now pre-recorded the course. Read about and purchase the eLearning course here
Pet supplements, foods and veterinary products. This is a new course under development. It replaces previous course “Agricultural and Veterinary Chemicals” and the new agenda will focus on pet supplements as we have had a lot of interest in this topic. It will be ready soon. If you have a particular interest in pet supplements and/or pet foods and would like to know when it is ready, please email info@regulatorytrainingdirect.com
AU Cosmetic Claims and Labelling has been updated, agenda is here.
View the agenda for all 40 courses and book online here. Some courses are available as live tuition, others are eLearning (pre-recorded), and some are available in both formats. When you purchase an eLearning course your password lasts for 60 days, so you can access the course as often as you want before the password expires
Regulatory affairs news
Complementary Medicines and Medical Devices
TGA website update
* What’s changed on the website? In particular, enhanced primary navigation, mega menus, what’s new. Published 30 October.
* How to use an RSS feed – you will need to download an RSS reader/aggregator. By connecting to RSS feeds, you are automatically informed, via the use of an RSS feed reader or aggregator, of website updates. Learn more here.
* How to use the business portal on TGA site: explains setting up your organisation, setting up and viewing your TGA contact people including the different capabilities for the user roles – drafter, submitter, financial and administrator. It is explained here.
Applying for use of a restricted representation in advertising: a compliance checklist and guidance for submitting an application published here.
Nitrosamine risk in listed medicines. Information for sponsors and manufacturers on assessing the risk. How do nitrosamine impurities form? How does this relate to botanicals and other naturally derived medicinal substances? A very helpful and detailed guideline published on 7 October available here.
TGA’s freedom of disclosure (FOI) log – last update is here.
Medicines and medical devices that have been cancelled or suspended – list updated October 2025 Source: TGA
GMP clearance Sponsor Information Dashboard was last updated 7 October.
Submit data in electronic common technical document (eCTD) format, for prescription medicines applications, and also biologicals, over-the-counter medicines, registered complementary medicines, assessed listed medicines and ingredients for listed medicines. eCTD cannot be used for medical devices and GMP applications. This is a comprehensive guide, updated 24 October and published here.
Recalls
* What do you do if your medicine is recalled? How to handle recalls; guideline updated 3 October.
* Phytologic Holdings is recalling one batch of Henry Blooms Infant Liquid D3 & K2 with Probiotic due to a dosing syringe error. The syringe graduations do not match the labelled paediatric dosages. More information here.
Compliance activity
* Compliance actions and outcomes. This is an updated information page to “Know the ways we respond to breaches such as warnings, fines and legal action”, updated 31 October.
* Enforceable directions – another revised information page updated 31 October
* Advertising directions and prevention notices information – updated 23 October.
* An enforceable direction has been issued to Hwangbo in relation to illegal supply of vaping goods from The Candy Store in Melbourne. More information available in either PDF or MS Word format here.
* An advertising direction has been issued to Hwangbo and Nabil Mouawad to cease all advertising of vaping goods at the Candy Store. Source: TGA
* An advertising direction has been issued to Adam Monza Hammoude and Iget Brandsto cease all unlawful advertising of vaping goods on all websites, social media accounts or other advertising platforms, including the advertising on the website at the URLs iget-vapes.com. Source: TGA
* Illegal vapes and cigarettes worth $9 million seized in joint operations in southeast Queensland. Source: TGA
* Infringement notices totaling $99,000 were issued to ACPharm Queensland for unlawfully advertising medicinal cannabis and other therapeutic goods that are not included in the Australian Register of Therapeutic Goods (ARTG). ACPharm Queensland paid the infringement notices in October. Source: TGA .
#MedSafetyWeek starts! TGA is joining forces with medicine regulators around the world to help spread the word about preventing and reporting side effects from medicines.
If you experience a side effect in Australia, you can report it to the TGA here: https://aems.tga.gov.au/. (We have a course on pharmacovigilance, read about it here)
Product correction: Mylife CamAPS FX app. – issues with software updates for both Apple and Android devices – The product’s Instructions for Use (IFU) did not provide adequate clarity on smart device and OS compatibility. More details here.
Vaping
* TGA has issued “a clear warning to online delivery service providers not to breach Australian laws regarding the supply and advertising of vaping goods” following complaints. Source: TGA
* Regulatory requirements for dispensing and supplying vapes in pharmacies. Outlines pharmacists’ regulatory responsibilities when supplying therapeutic vapes to support patients in quitting smoking or managing nicotine dependence. Recently published on 10 October.
Public and stakeholder consultation:
* The GMP Guidelines on Chapter 1 – Pharmaceutical Quality System are being updated to reflect contemporary Quality Risk Management principles and further improve how Product Quality reviews are performed. Public consultation is now open and closes on 3 December. Read more here. You can provide feedback here.
* Digital Mental Health Tools – software-based medical devices – including digital mental health tools (DMHTs) – are used to screen, diagnose, monitor and/or treat patients experiencing mental health conditions. Due to growing interest in using software and artificial intelligence (AI) TGA is seeking information. Read more here.
* Expression of Interest – TGA regulatory Forum 2027. TGA is inviting stakeholders across the therapeutic goods sector including sponsors, regulatory agents and manufacturers of medicines, biologicals and medical devices to complete their Expression of Interest (EOI) form for the inaugural TGA Regulatory Forum 2027. Deadline is Friday 28 November. Survey form is here.
Template for uploading Unique Device Identification numbers to the Australian UDI Database (AusUDID) – available in Excel format – updated 30 October
Enhancements and fixes to the AusUDID Pre-Production environment. Latest details released 29 October,
Resources and technical documents for Machine to Machine (M2M) HL7 SPL users in the Australian Unique Device Identification Database (AusUDID), updated 30 October
Companion diagnostics (CDx) approved for supply in Australia. A CDx is an in-vitro diagnostic (IVD) medical device that provides information essential for the safe and effective use of a corresponding medicine or biological. List of approved devices available here.
Breast implant hub has the latest information on breast implants, updated 16 October.
Breast implants with micro transponders: a post-market review is underway as when these implants are exposed to magnetic resonance imaging (MRI), the micro transponder interferes with the magnetic field generated by MRI. The interference of these devices with MRI of the thorax (chest), including breasts and surrounding tissues and organs, results in image distortions. This can prevent important details being displayed in the scan such as whether the implant has ruptured, if there is a lesion, or other issues that requires attention. More information here:
EU MDR Transition web publication service is a platform for sponsors to provide market notifications to health care providers and consumers for devices going through low-risk changes as part of the EU MDR Transition. Updated 7 October.
TGA contact details – email, phone, fax,. post, social media channels – have been updated.
New Zealand Ministry of Health – update on the regulation of medicines, medical devices and natural health products. Includes some changes to advertising rules, including allowing products without a Medsafe approval to be promoted at medical conferences and trade shows. Plus other proposed changes which will be in the revised Medical Products Bill. The Government is also considering how best to regulate natural health products. (Editor’s note: this information is contained in their newsletter “Medical products and natural health products update” which I could not find on their website. You can subscribe to this newsletter here: subscribe to this newsletter. Alternatively email me at robert@regulatorytrainingdirect.com and I will forward you my copy)
Botanical Adulterants Prevention Programme (BAPP) and other adulteration stories.
* Amazon Sued for Allegedly Allowing Fake Products That Harmed Consumers(contributed by Michael D Levin, Health Business Strategies, LLC). A group of plaintiffs across multiple (US) states has filed a lawsuit accusing the retail giant of negligence, deceptive practices, and failure to protect the public from third-party sellers who list fake, unsafe, or untested goods. Article published on Shepherd & Allen website.
* Botanical Adulterants Monitor – latest issue #33- read it here.
For feedback on SupplySide Global see below under “other news”.
For regular news on US dietary supplement and food regulation, go to AWG Regulatory Roundup.
IN THE PRESS
* The deported kingpin, the Chinese gang and the vape brand controlling an Australian black market. Australia’s illegal tobacco cartel has joined forces with a mysterious Chinese crime gang to infiltrate and control the local vape market. Source: Sydney Morning Herald
* Formaldehyde and antifreeze: What’s inside one of the most popular illegal vapes in Australia. One of the most popular vape brands in Australia, Alibarbar, is delivering flavoured puffs with potentially dangerous levels of nicotine and toxic contaminants, including the embalming fluid formaldehyde and a chemical used in making antifreeze. Source: Sydney Morning Herald
Foods
Allergen labelling for food businesses. Details new requirements, lists foods and ingredients to be declared and how they must be declared, cereals containing gluten, bee products, and has a link to an allergen labelling poster. Source: FSANZ
2-hour / 4-hour rule – make sure potentially hazardous food is safe even if it’s been out of refrigeration. Explains what you can do with food when ti has been out of refrigeration for less than 2 hours, between 2 and 4 hours, or more than 4 hours. Has a downloadable poster. Source: FSANZ
No evidence that blueberries from Northern NSW are unsafe to eat. Following articles in the media that they may be contaminated with thiometon, a review by the NSW Food Authority and the NSW Environment Protection Authority (EPA) showed no evidence of thiometon residue on any berries tested. Source: NSW Food Authority
Agents of foodborne illness. A technical series containing information about pathogens that cause foodborne illness. Source: FSANZ
Amendments to Food Standards Code: the following amendments have been published:
As a result of the application for the use of new enzyme processing aids derived from genetically modified E. coli BL21, to produce the steviol glycoside rebaudioside M:
* Schedule 3 Identity and purity
* Schedule 18 Processing aids
Approvals (none in October)
New applications and proposals
* FSANZ has completed an administrative assessment and accepted the application for Cell-cultured duck (Anas platyrhynchos domesticus) biomass as a food ingredient for use in duck meat analogues such as foie gras and pate. Administrative assessment report is here and executive summary is here.
Public consultations and calls for submissions/comments
* FSANZ invites responses for the Nutrition Information Panel (NIP) Review – preliminary position paper. Submissions close on 30 November 2025 at 11:59pm Read more here.
* Caffeine review: FSANZ invites submissions on a revised draft variation to the Code, s in relation to permissions for caffeine in sports foods and in the general food supply. Consultation closes 12th December. More here.
* FSANZ is calling for comment on an application to permit a new genetically modified source organism to produce a human-identical milk oligosaccharide used in infant formula products. Consultation closes 18th November. Source: FSANZ
Novel foods determinations – entries added after the last update include:
* Green tree ants – (Oecophylla smaragdina) – determined to be a traditional indigenous food, not a novel food; but note the comments that include reference to allergy.
* Lion’s mane (Hericium erinaceus) – in fresh form – determined to be a non-traditional food, and a novel food, needing assessment
* Mopane worms – (Gonimbrasia belina) in whole dried form – determined to be a non-traditional food, and a novel food, needs assessment and potential for allergenicity.
* Mycoprotein biomass from Neurospora crassa – determined to be a non-traditional food, and a novel food, needing assessment.
Latest version of novel foods determination is published here.
Recalls
* Lion Beer – Little Creatures Little Hazy Lager 375mL – Secondary fermentation which can lead to over-pressurisation of the can. More here
* Muscle Nation Supplements – Custard Protein Bar Cookies and Cream – due to presence of undeclared allergen (gluten) on the outer display box. More here
* Link Foods Australia – Golden Island Pork Jerky Korean BBQ Recipe – presence of foreign matter (metal). More here
* Moncha Wholesale – S&B Savory dish chilli oil – presence of undeclared allergens (almond, walnut). More here
* Riviana Foods – FEHLBERGS Pickled Sliced Jalapenos Chilli Medley – presence of foreign matter (glass) More here
* Sea to Summit – Back Country Cuisine – Spaghetti Bolognaise & Mushroom Bolognaise – presence of an undeclared allergen (egg). More here
* ‘Aquaman the Lost Kingdom‘ 24oz double wall cup with LED electroplated lid and straw. – the product is missing warning information about the dangers of button/coin batteries to children; and what to do when a person suspects someone has swallowed or placed a button/coin battery inside any part of their body. Source: ACCC Product Safety
* Sonic 3 plastic cup featuring an LED light and straw. – the product is missing warning information about the dangers of button/coin batteries to children; and what to do when a person suspects someone has swallowed or placed a button/coin battery inside any part of their body. Source: ACCC Product Safety
Additional food news supplied by Correct Food Systems
NSW has updated the Food Regulation from 2015 to 2025 version. Key changes are:
* tighter timeframes in the NSW Food Safety Schemes manual to report unsatisfactory microbiological test results.
* Food testing laboratories must report any food samples that fail set microbiological standards to the Food Authority in writing within 24 hours of completing the analysis
* Increased financial penalties and charges
* Licencing requirements for melon, berry, leafy vegetables businesses from 12 February 2026.
* Increased controls for Salmonella Enteritidis by licenced egg producers
* FSS students to complete training course with one RTO
(Note from editor: email lisa@correctfoodsystems.com.au if you would like to receive their newsletter)
New Zealand Food safety insights, emerging risks, and current issues bulletins:
These bulletins contain news from all over the world. Latest issues: 10th October and 24th October. Worth reading, lots of overseas news.
**New Zealand food recalls**
* Piper’s brand **Milkshake Biscuits in Original and Caramel flavours** – presence of an undeclared allergen (pistachio). *Source: MPI New Zealand*
* Smartfoods Limited – **Tom** & **Luke brand Protein Peanut Brownie Snackaballs, Vogel’s brand Cluster Crunch Peanut Butter** and **Vogel’s brand Daily Protein Plus Almond Pistachio** – may contain **foreign matter (small metal pieces)**. *Source: MPI New Zealand*
* Hancook brand **Sundae (Korean black sausage)** – due to **lack of required food safety controls**. *Source: MPI New Zealand*
* **Back Country Cuisine Mushroom Bolognaise and Spaghetti Bolognaise**, due to the presence of an **undeclared allergen (egg)**. *Source: MPI New Zealand*
* King Salmon- **Regal Marlborough King Sa**l**mon Dip with Gherkins, Capers & Dill** – product labelled with an** incorrect Use-By date. ***Source: MPI New Zealand*
* New World Te Kuiti – made-in-store Pams Hot Roasted Chickens sold on 23 October 2025 – may have been **contaminated by a cleaning chemical. **_Source: MPI New Zealand_
* Link Foods New Zealand – **Golden Island brand Pork Jerky Korean BBQ Recipe** – may contain **foreign matter (metal**)._Source: MPI New Zealand_
For regular news on **US dietary supplement and food regulation**, go to *Regulatory Roundup*.
*IN THE PRESS*
* **Social media promotion of raw milk ‘misleading and dangerous’**. It is illegal to sell raw or unpasteurised milk for human consumption in Australia because it may contain harmful pathogens. In the US state of Florida, 21 people became sick from campylobacter and E.coli and seven were hospitalised in August, after consuming raw milk from the same dairy. *Source: ABC.net.au*
**Cosmetics and sunscreens**
* Additional information updated 31 October: **Sunscreens using the same base formulation as Ultra Violette Lean Screen SPF 50+ sunscreen** – an update with more information about TGA’s concerns about the SPF of the Lean Screen base formulation. The TGA states “The preliminary testing indicates that this base formulation is unlikely to have an SPF greater than 21. Preliminary testing of specific goods manufactured using the base formulation indicate that the SPF value of the goods may, for at least some of the goods, be as low as SPF 4.” The manufacturer has ceased manufacture and supply of the base formulation. The TGA “has significant concerns about the reliability of SPF testing undertaken by Princeton Consumer Research Corp (PCR Corp), a testing laboratory based in the United Kingdom”. *Source: TGA*
**Sunscreens not meeting their claimed SPF rating**. Our colleague John Staton (the international “guru” of all things to do with sunscreens), has developed an audit kit to help evaluate SPF test results. The kit consists of 3 parts:
* A SciPharm SPF QuickCheck worksheet for evaluation of the data for the individual test subjects
* SciPharm SPF Reporter – a set of spreadsheets which are designed to evaluate the compliance of the test report with the ISO Norm
* A PowerPoint for training and overview of the core principles and steps of the test methodology.
*(Editor: I have had a look at what John is offering, and if you are involved with the manufacture and marketing of sunscreens, I strongly advise you to consider purchasing this kit from John)*. You can contact John at johnstaton@scipharm.com.au
**AICIS improved log in page **_- see what’s changed – info here_
**PFAS – have you introduced any PFAS chemicals to Australia**? If you have, it is important you note this statement on the AICIS website: “On 21 October 2025, the AICIS Executive Director initiated an evaluation on the introduction and use of 522 per- and poly-fluoroalkyl substances (PFAS) in Australia. Everyone registered with us between 1 September 2023 and 31 August 2025 was sent a notice about the requirement with a unique link to an online form to provide us information.” Read more about your obligations on the AICIS website *here*.
**** **It’s time to submit your annual declaration for 2024–25. Due by 30th November. ***This page* includes who must make an annual declaration for 2024–25 and how to submit an annual declaration.
AICIS “Rolling Action Plan” has been updated to include an **evaluation on the introduction and use of 522 per- and poly-fluoroalkyl substances (PFAS)** You can find details *here*.
**Consultation on proposal to vary inventory terms of listing** for:
* azo dyes based on 5-nitro-2-thiazolamine and toluenediamine derivatives (EVA00166)
and
* 2-propenoic acid, 2-methyl-, 1,1′-(1-methylethylidene)di-4,1-phenylene ester (Bisphenol A dimethacrylate) (EVA00179).
Closes on 28th November, *read more here*.
**Designated fluorinated chemicals** – information required. *Source: AICIS*
**The latest inventory snapshot August 2025 ***available for download here.* the most recent industrial chemicals inventory is *here*.
**Variation of Inventory listing** following revocation of CBI approval (obligations apply), as at 14th October: CAS 3099978-68-1 *(a soybean oil)*. Read more *here*.
**List of new chemical assessment statements**
as at 15th October: 7 chemicals are listed *here*. Two are included in personal care products:
* CA10011 – (Butanal, 4-(3,3,4-trimethylcyclopentylidene)-, (4E)-) and
* CA10025 (2H-2,4a-Methanonaphthalen-1(5H)-one, hexahydro-5,5-dimethyl-2-propyl-, (2R,4aR,8aS)-rel-) *(editor’s note: that’s a very long word, on a par with antidisestablishmentarianism and supercalifragilisticexpialidocious)*
**Chemicals added to the Inventory **5 years after issue of assessment certificate (obligations to provide information apply)
* as at 20 October – CAS 1000172-32-6 – *AICIS*
**Recalls**
* Various cosmetics sold by **W Cosmetics – t**he product labels do not meet the mandatory standard for cosmetics ingredients labelling, the ingredients lists on the cosmetic and skincare products are not in English. There is a risk of allergic reaction if consumers are exposed to ingredients they are sensitive or allergic to. More information on ACCC *product safety website*, view the huge list (11 pages long) of affected products *here.*
* Bunjie **Peek-A-Boo Probiotic Baby Eye Wipes** – the package may not have been properly sealed during manufacturing, which may lead to mould growth. Risk of allergic reaction and illness, including skin and eye irritation or infection, if mould is present in a wipe that is used on skin. Individuals with sensitive skin or weakened immune systems may be at greater risk. Incidents have occurred. Read more at ACCC *product safety website*.
*IN THE PRESS*
* .**Beauty brands ordered to stop selling products with banned ingredient**. This headline in the Sydney Morning Herald refers to the sale of cosmetics containing microbeads. The brands ordered to withdraw products from sale in NSW are Aesthetics Skincare Bio Fermented Triple Action Scrub; Coles Group KOi for Men Cleansing Face Scrub and Desert Lime; Frostbland Alya Skin Pomegranate Facial Scrub and Exfoliating Sorbet; JMSR Australia Jan Marini Bioglycolic Resurfacing Body Scrub, and Jan Marini Cranberry Orange Exfoliator; McPherson’s Consumer Products Dr LeWinn’s Essentials Gentle Exfoliant Weekly Facial Polishing Gel; Natio for Men Purifying Face Scrub, and Natio Ageless Skin Renewal Exfoliator. *Source: Sydney Morning Herald*
* **Botox, fillers among the cosmetic injectables targeted in medical regulator’s new rules**. Includes “What are the new rules for cosmetic injectables and other procedures?”, “Influencers under the spotlight”, “What qualifications do you need to administer cosmetic injectables?’ and more. *Source: ABC.net.au *
* **Australian SPF Controversy Heats Up**. *Source: Happi/New York Times*
* **The Real Sunscreen Scandal Isn’t in Australia. It’s in the Lab**. *Source: Beauty Matter.*
**Cosmetics in Europe **_contributed by Steven Hanft, Conusbat_
_Cosmetics Consultants Europe’s (CCE) continuation for Cosmetic Product Safety Assessment Online Training_
Module 3: ‘Toxicology 2’
* Begins: Tues., 11. Nov. 2025 | 12EST 17GMT 18-19.30CET – Fee: €1.400-/Module (purchase all 6 modules, get 1 Free!)
* Register: https://www.ccecosmetic.org/cce-training-courses/
Contact: Steven L. Hanft, M.A., Bus. Communications, CCE > steven.hanft@cpsr-education.com
* Register here or enquiries to Steven Hanft on this email.
_NOTE: **Subscribers to this newsletter receive a discount**_
**ACCC and other news**
The ACCC has today commenced civil proceedings in the Federal Court against four suppliers and three senior executives for **alleged price fixing while supplying fresh produce,** including broccoli, cauliflower, iceberg lettuce, cucumber, Brussels sprouts and zucchini, to ALDI stores in New South Wales, Victoria and Queensland between 2018 and 2024, in breach of Australia’s cartel laws. Full details on ACCC website *here*.
**New Zealand Ministry for Regulation**. Our colleague Dr David Buckley has brought our attention to the newsletter and annual report published by the NZ Ministry. You can see the newsletter at *this webpage*. This page has links to topics that may be of interest to our readers such as the review of New Zealand’s product labelling rules. The annual report 202-2025 is available in PDF format *here*.
**Funding and Support for Industry **_contributed by Gary Kennedy, Correct Food Systems_
A few new programs have opened under the Australian Government’s AusIndustry network:
• Food and Beverage Accelerator (FaBA) Kickstarter Vouchers: SMEs can apply for up to $50,000 (with 10–20% matching funding) to support product development, market analysis and commercialisation.
• Powering the Regions Round 3: $180 million available to support industrial decarbonisation projects, including electrification, energy efficiency, and fuel switching.
• TRaCE Concept to Pilot: Co-funding of up to $200,000 to validate or scale clean energy or recycling innovations.
* AusIndustry has also released short information videos to help applicants navigate the grants process, and the Net Zero for SMEs webinar offers further guidance for businesses looking to reduce emissions and improve efficiency. These initiatives provide practical, government-backed pathways for businesses to invest in sustainability, innovation, and future readiness.
**SupplySide Global 2025**
Last week our Director & Co-Founder Abbie Harris attended SupplySide Global 2025. This annual tradeshow held in Las Vegas is the ultimate destination for professionals in the supplement, food and beverage, pet health and cosmetic industries.
Bursting with over 20,000 attendees and 1,600 exhibitors the event presents limitless opportunities to soak up education, next-level networking as well as innovation and compliance themes that are shaping the future of the industry.
Buzzing themes at the event included:
* **Healthy longevity** – spanning many categories focused on extending healthspan. Recent research proposes twelve hallmarks of aging.
* **Biotic ingredients** for targeted health benefits. Research in the US showed that consumers taking probiotics nearly tripled over the past decade. The International Probiotic Association booth was teeming with exciting pre- post- and pro- biotic ingredients.
* **Weight management** remained prominent with Berberine and GLP-1 agonist support products in the spotlight.
* **Evidence-backed** ingredients supported by clinical studies are increasing.
* **Experiential products** that deliver fast-acting benefits or innovative delivery formats.
* **Creatine** – with surging consumer demand, SupplySide showcased the benefits beyond muscle growth and use in novel dosage forms.
* **Product Quality, Safety & Compliance** – the underbelly to the industry was discussed in education sessions and impromptu meetings. Important issues included poor quality raw materials, lack of appropriate testing or temperature control of goods, non-compliance and the rise in fake clinical trials. Esteemed industry guardians advocated strategies to stamp out fraudulent players.
Being a US-based tradeshow, bringing innovations and concepts to Australia or other markets is not always straight-forward (or possible) as international regulations differ vastly across regions. If you want to upskill your compliance knowledge to assess suitability of ingredients or evidence for your products in Australia, New Zealand, or the USA check out our online training courses here.
Published by Regulatory Training Direct www.regulatorytrainingdirect.com
Providing regulatory training courses for complementary medicines, medical devices, GMP, foods, cosmetics, dietary supplements.
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