Distribution date: 07 April 2021 | Final date for Comment: 13 May 2025

The proposed maximum residue limits (MRLs) for Bixafen notified in G/SPS/N/JPN/785 (dated 19 October 2020) were adopted and published on 3 February 2021.The specified MRLs are available as below:

Products Covered:

Regulation Type: Addendum to Regular Notification

Distribution date: 07 April 2021 | Final date for Comment: 13 May 2025

The proposed maximum residue limits (MRLs) for Pyriproxyfen notified in G/SPS/N/JPN/788 (dated 19 October 2020) were adopted and published on 3 February 2021.The specified MRLs are available as below:

Products Covered:

Regulation Type: Addendum to Regular Notification

Distribution date: 07 April 2021 | Final date for Comment: 06 June 2021

This Compulsory Specification requires that frozen lobsters and frozen lobster products derived therefrom for direct consumption or further processing, which are to be offered for sale, comply with this Compulsory Specification and the requirements of the latest edition of the South African National Standard (SANS) 2074 which applies to the manufacture, production, processing, and treatment of the products covered by this specification. The hygiene requirements for the product, as well as chemical and microbiological contaminant requirements for the product, and the requirements for employees at the packing facility, shall comply with the requirements of the latest edition of SANS 2074.

Products Covered: Frozen lobster, frozen lobster products and products derived therefrom, i.e. HS Codes: 03 and 16

Regulation Type: Regular notification

Distribution date: 07 April 2021 | Final date for Comment: 06 June 2021

This standard specifies terms and definitions, requirements, test methods and inspection rules for inert gas agents. This standard is applicable to inert gas agents.

Products Covered: Inert gas agent

Regulation Type: Regular notification

Distribution date: 07 April 2021 | Final date for Comment: 06 June 2021

This part of GB 7300 specifies the requirements, sampling, test methods, inspection rules, labelling, packaging, transportation, storage and shelf life of feed additive potassium iodate. The standard is applicable to feed additive potassium iodate prepared by potassium chlorate oxidation method and electrolysis method. All technical contents of this part are mandatory.

Products Covered: Feed additive Potassium iodate

Regulation Type: Regular notification

Distribution date: 07 April 2021 | Final date for Comment: 13 May 2025

The purpose of this Notice of Intent to Amend is to notify stakeholders that Health Canada will remove tramadol from both the Human and Veterinary sections of the Prescription Drug List when the addition of tramadol to Schedule I to the Controlled Drugs and Substances Act and to the Narcotic Control Regulations comes into force on 31 March 2022. 

Products Covered: Prescription status of medicinal ingredients for human use

Regulation Type: Regular notification

Distribution date: 08 April 2021 | Final date for Comment: 07 June 2021

This Compulsory Specification requires that frozen lobsters and frozen lobster products derived therefrom for direct consumption or further processing , which are to be offered for sale, comply with this Compulsory Specification and the requirements of the latest edition of the South African National Standard (SANS) 2074 that apply to the manufacture, production, processing, and treatment of the products covered by this specification. The hygiene requirements for the product, as well as chemical and microbiological contaminant requirements for the product, and the requirements for employees at the packing facility, shall comply with the requirements of the latest edition of SANS 2074.

Products Covered: FISH AND CRUSTACEANS, MOLLUSCS AND OTHER AQUATIC INVERTEBRATES (HS code(s): 03); PREPARATIONS OF MEAT, OF FISH OR OF CRUSTACEANS, MOLLUSCS OR OTHER AQUATIC INVERTEBRATES (HS code(s): 16); FOOD TECHNOLOGY (ICS code(s): 67); Fish and fishery products (ICS code(s): 67.120.30)

Regulation Type: Regular notification

Distribution date: 08 April 2021 | Final date for Comment: 07 June 2021

The notified Ecuadorian Technical Regulation establishes the requirements to be met by toys, prior to the marketing of domestic and imported products, with the aim of protecting human health and safety and preventing deceptive practices. It applies to the following products: Toys intended for use by children under 14 years of age. The Technical Regulation does not apply to: 1. Home and public playground equipment; 2. Automatic playing machines, whether coin-operated or not, intended for public use; 3. Toy vehicles equipped with combustion engines; 4. Toy steam engines; 5. Slings and catapults; 6. Decorative objects for festivities and celebrations; 7. Products for collectors, provided that the product or its packaging bears a visible and legible indication that it is intended for collectors of 14 years of age and above; 8. Sports equipment including roller skates, inline skates, and skateboards intended for children with a body mass of more than 20 kg; 9. Bicycles with a maximum saddle height of more than 435 mm, measured as the vertical distance from the ground to the top of the seat surface, with the seat in a horizontal position and with the seatpost set to the minimum insertion mark; 10. Scooters and other means of transport designed for sport or which are intended to be used for travel on public roads or public pathways; 11. Electrically driven vehicles which are intended to be used for travel on public roads, public pathways, or the pavement thereof; 12. Aquatic equipment intended to be used in deep water, and swimming learning devices for children, such as swim seats and swimming aids; 13. Puzzles with more than 500 pieces; 14. Guns and pistols using compressed gas, with the exception of water guns and water pistols; 15. Bows for archery over 120 cm long; 16. Fireworks, including percussion caps which are not specifically designed for toys; 17. Products and games using sharp-pointed missiles, such as sets of darts with metallic points; 18. Functional educational products, such as electric ovens, irons or other functional products operated at a nominal voltage exceeding 24 V which are sold exclusively for teaching purposes under adult supervision; 19. Products intended for use for educational purposes in schools and other pedagogical contexts under the surveillance of an adult instructor, such as science equipment; 20. Electronic equipment, such as personal computers and game consoles, used to access interactive software and their associated peripherals, unless the electronic equipment or the associated peripherals are specifically designed for and targeted at children and have a play value on their own, such as specially designed personal computers, key boards, joy sticks or steering wheels; 21. Interactive software, intended for leisure and entertainment, such as computer games, and their storage media, such as CDs; 22. Babies' soothers; 23. Child-appealing luminaires; 24. Electrical transformers for toys; 25. Fashion accessories for children which are not for use in play; 26. Personal protective equipment, including flotation aids such as arm bands and swim seats, and swimming goggles, sunglasses and other eye protectors as well as bicycle and skateboard helmets; 27. Sporting goods and equipment, camping goods, athletic equipment, musical instruments and furniture; however, toys which are their counterparts are included; 28. Toys installed in public places (e.g. arcades and shopping centres); 29. Fashion jewellery for children. 30. This Ecuadorian Technical Regulation does not cover electrical safety aspects of toys.

Products Covered: Tricycles, scooters, pedal cars and similar wheeled toys; dolls' carriages; dolls; other toys; reduced-size "scale" recreational models, working or not; puzzles of all kinds (HS code(s): 9503); Equipment for children (ICS code(s): 97.190); Toys (ICS code(s): 97.200.50)

Regulation Type: Revision to Regular Notification

Distribution date: 09 April 2021 | Final date for Comment: 05 May 2021

We are considering regulation to require the validation of all Covid-19 detection tests for human use made available for private sale. This would set minimum quality standards for specificity and sensitivity against which Covid-19 tests would be assessed. This would prevent retailers from selling tests that haven’t been validated to meet this standard and place a requirement on manufacturers to seek validation for their tests. There would potentially be a broad suite of enforcement powers up to and including criminal sanction. The intention would be to place the results of each test’s validation in the public domain to inform consumer choice. In scope will be mature antigen detection and molecular detection technologies, as such the  main tests we expect to be assessed are Lateral Flow Tests, and Polymerase chain reaction (PCR) tests. Given the urgency and the set up times we envisage doing this via a single government run process.

Products Covered: HS3822

Regulation Type: Regular notification

Distribution date: 09 April 2021 | Final date for Comment: 13 May 2025

ANVISA issued RDC No. 489, 7 April 2021, that amends the Collegiate Board Resolution - RDC No. 483, of 19 March 2021, previously notified through G/TBT/N/BRA/1154, which provides, in an extraordinary and temporary way, on the requirements for the importation of new medical devices and medicines identified as priorities for use in health services, due to the international public health emergency related to SARS-CoV-2. The final text is available only in Portuguese and can be downloaded at: http://antigo.anvisa.gov.br/documents/10181/6245812/RDC_489_2021_.pdf/50ae8d42-0a2f-4758-864a-820a52f60827

Products Covered: Provitamins and vitamins, natural or reproduced by synthesis, incl. natural concentrates, derivatives thereof used primarily as vitamins, and intermixtures of the foregoing, whether or not in any solvent (HS code(s): 2936); Hormones, prostaglandins, thromboxanes and leukotrienes, natural or reproduced by synthesis; derivatives and structural analogues thereof "incl. chain modified polypeptides", used primarily as hormones (HS code(s): 2937); Antibiotics (HS code(s): 2941); PHARMACEUTICAL PRODUCTS (HS code(s): 30); Pharmaceutics (ICS code(s): 11.120)

Regulation Type: Addendum to Regular Notification