Resolution – RDC number 328, 19 December 2019

Distribution date: 10 January 2020
The Draft Resolution number 658, 24 June 2019, regarding maximum residue limit (MRL) of veterinary drugs in food of animal origin – previously notified through G/SPS/N/BRA/1528 – which establishes the procedure for risk assessment of veterinary drugs to human health and the methods for conformity assessment procedures, was adopted as Resolution – RDC number 328, 19 December 2019. The final text is available only in Portuguese and can be downloaded at: http://portal.anvisa.gov.br/documents/10181/5545276/RDC_328_2019_.pdf/c8530bf9-5c55-43fa-ae38-4d8aeff71270
Products Covered: HS Code(s): 30049085 (Veterinary medicinal preparations, not for human use, not elsewhere specified or included); ICS Code(s): 13, 65
Regulation Type: Addendum to Regular Notification
Normative Instruction number 51, 19 December 2019

Distribution date: 10 January 2020
The Draft Normative Instruction number 659, 24 June 2019, regarding maximum residue limit (MRL) of veterinary drugs in food of animal origin – previously notified through G/SPS/N/BRA/1527 – which establishes the MRL for veterinary drugs in food of animal origin, was adopted as Normative Instruction number 51, 19 December 2019. The final text is available only in Portuguese and can be downloaded at: http://portal.anvisa.gov.br/documents/10181/5545276/IN_51_2019_.pdf/15986ce9-1636-4060-8ffb-ae49be5d5207
Products Covered: HS Code(s): 30049085 (Veterinary medicinal preparations, not for human use, not elsewhere specified or included); ICS Code(s): 13, 65
Regulation Type: Addendum to Regular Notification
DUS DEAS 1022:2019, Hacksaw blades — Specification, First Edition.

Distribution date: 10 January 2020 | Final date for Comment: 10 March 2020
This draft Uganda Standard specifies the requirements, sampling and test methods for hand and machine hacksaw blades.
Products Covered: Hacksaw blades
Regulation Type: Regular notification
Joint Normative Instruction number 1, 8 November 2019.

Distribution date: 10 January 2020
This joint normative instruction establishes the guidelines for the market authorization of pesticides and related products designed to the cultivation of ornamental plants as well as for the inclusion of products already authorized.
Products Covered: HS Code(s): 06, 0603, 0604, 38089910; ICS Code(s): 13, 65
Regulation Type: Regular notification
SI 4272 - Oven cleaners and grease removers - Safety, packaging and marking requirements

Distribution date: 09 January 2020 | Final date for Comment: 09 March 2020
Revision of the Mandatory Standard SI 4272, dealing with the safety, packaging and marking requirements for oven cleaners and grease removers. The major differences between the old edition and this new revised draft standard are as follow: Moves a few of the packaging requirements to Israel Mandatory Standard SI 2302 part 1; Adds to paragraph 2.2.7 an instruction for the maximum temperature of the surface intended to be cleaned; Changes the safety requirements according to the European Directive EC 1272/2008. All sections of the draft standard revision will be mandatory after its entry into force, except for the requirements relating to the warning label "Do not eat" appearing in paragraph 2.2.9.Both the old standard and the new revised standard will apply for a period of 3 years from the date of entry into force. During this time products may be tested for compliance according to the old or the new standard's edition.
Products Covered: Oven cleaners and grease removers
Regulation Type: Regular notification
DUS DEAS 936: 2019, Gloss solvent borne paints for interior and exterior use — Specification, First Edition

Distribution date: 09 January 2020 | Final date for Comment: 09 March 2020
This Draft Uganda Standard specifies requirements, methods of sampling and test for three grades of gloss solvent-borne paints for interior and exterior use. This standard does not apply to automotive, road marking and Industrial applications.
Products Covered: Gloss solvent borne paints
Regulation Type: Regular notification
The draft guidelines for the assessment of the quality and research of drugs based on liposomes, micelles and drug-containing coating of nanoparticles.

Distribution date: 09 January 2020 | Final date for Comment: 25 March 2020
The draft guidelines for quality assessment and research of liposome-based drugs, micelles and drugs containing nanoparticle coatings apply to the development of copied drugs from the liposome, micelle and drug group, containing nanoparticle coatings for subsequent registration on the territory of the Eurasian economic Union and provides for the need to establish uniform requirements for the evidence-based study of the equal effectiveness and interchangeability of copied and reference drugs based on liposomes, micelles and drugs containing nanoparticle coatings used in the treatment and prevention of human diseases, in order to: identification of ineffective and (or) non-equivalent drugs at the pre-registration stage, resulting in the risk of harm to human life and health; elimination of the need to duplicate studies of these groups of drugs in each of the member States of the Union. The draft guide has been prepared in order to: - protection of life and health of the patient (as the final consumer of medicines); - protection of the interests of the health care system as a whole (as the primary consumer of medicines) by ensuring the use of proven equally effective and interchangeable copied medicines; - protection of the interests of patients participating in the study by clearly regulating the procedure for conducting bioequivalence studies of these groups of drugs.
Products Covered: Medicaments consisting of mixed or unmixed products for therapeutic or prophylactic uses, put up in measured doses "incl. those in the form of transdermal administration" or in forms or packings for retail sale (excl. goods of heading 3002, 3005 or 3006) (HS code(s): 3004); Opacifying preparations for x-ray examinations; diagnostic reagents for administration to patients (HS code(s): 300630); Medicaments (ICS code(s): 11.120.10)
Regulation Type: Regular notification
"Productos Cosméticos" La República de Ecuador comunica en relación con el Reglamento Técnico Ecuatoriano RTE INEN 093 (1R) “Productos Cosméticos”, notificado mediante documento identificado con la signatura G/TBT/N/ECU/111/Add.2 del 8 de diciembre de 2015, ha sido suspendido y declarado sin aplicabilidad; por lo tanto queda insubsistente. Texto disponible en el Ministerio de Producción, Comercio Exterior, Inversiones y Pesca, Subsecretaría de Calidad, Organismo Nacional de Notificación: Punto de Contacto OTC: Andrés Ramón Plataforma Gubernamental de Gestión Financiera - Piso 8 Bloque amarillo Av. Amazonas entre Unión Nacional de Periodistas y Alfonso Pereira Quito - Ecuador Tel: (+593-2) 3948760, Ext. 2252/2254 E-mail: [email protected] [email protected] [email protected] [email protected]

Distribution date: 09 January 2020
Products Covered: 3303.00.00.00, 3304.10.00.00, 3304.20.00.00, 3304.30.00.00, 3304.91.00.00, 3305.10.00.00, 3305.20.00.00, 3305.30.00.00, 3305.90.00.00, 3306.10.00.00, 3306.90.00.00, 3307.10.00.00, 3307.20.00.00, 3307.30.00.00, and 3307.90.90.00. ;Perfumes and toilet waters (HS 330300); Lip make-up preparations (HS 330410); Eye make-up preparations (HS 330420); Manicure or pedicure preparations (HS 330430); Powders, whether or not compressed (HS 330491); Shampoos (HS 330510); Preparations for permanent waving or straightening (HS 330520); Hair lacquers (HS 330530); Other (HS 330590); Dentifrices (HS 330610); Other (HS 330690); Pre-shave, shaving or after-shave preparations (HS 330710); Personal deodorants and antiperspirants (HS 330720); Perfumed bath salts and other bath preparations (HS 330730); Other (HS 330790). ;
Regulation Type: Addendum to Regular Notification
Draft Resolution number 760, December 27th, 2019. Number of pages: 38; Language(s): Portuguese Draft: Comment form: http://formsus.datasus.gov.br/site/formulario.php?id_aplicacao=52824

Distribution date: 09 January 2020 | Final date for Comment: 07 April 2020
This Draft Resolution establishes the minimal technical requirements for relative bioavailability and bioequivalence studies that supports dossier of consent for clinical research, market authorization or post-market authorization of medicines, in the terms of this resolution.
Products Covered: HS Code(s): 3003; 3004; 3005; 2941 (pharmaceutical products).
Regulation Type: Regular notification
DUS DEAS 1016:2019, Textiles — Maasai Shuka — Specification, First Edition.

Distribution date: 09 January 2020 | Final date for Comment: 09 March 2020
This Draft Uganda standard specifies the requirements, sampling and test methods of Maasai Shuka.
Products Covered: Maasai Shuka
Regulation Type: Regular notification
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