in Tag: Complementary Medicines  (clear all)


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SAFETY-RELATED PACKAGE INSERT NOTIFICATIONS (SR-PINs) - (MCC: Aug 17)

Safety-related Package Insert Notifications (SR PINS) in South Africa.Circular 2.17.

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event,   Post-marketing

CAMs Specified Substances 7.06 v2, Jun 2018

COMPLEMENTARY MEDICINES GUIDANCE ON SPECIFIED SUBSTANCES

Related Tags (New Search): Complementary medicines

Complementary Medicines: Right to Sale (MCC: 9.72, Apr 2016)

Publication of Complementary Medicines (Category D) Submitted for Registration terms of Section 14(3) of the Medicines and Related Substances Act, 1965 (Act 101 of 1965). Please note that this is a third-party website. Juta has no control over the nature,…

Related Tags (New Search): Complementary medicines

ROADMAP FOR REGISTRATION OF COMPLEMENTARY MEDICINES

This document has been prepared to serve as a recommendation to applicants wishing to register complementary medicines for which claims of safety, quality and efficacy are being made and which have been called up for registration. It represents the Medicines…

Related Tags (New Search): Complementary medicines,   Health supplements

MCC Resolution to rescind call-up (2002) of complementary medicines

The call-up notice R204, Gazette No 23128 of 22nd February has been rescinded by resolution published in Gazette 40637 of 24 February 2017.

Related Tags (New Search): Complementary medicines

Roadmap for Registration of Complementary Medicines (MCC: 7.02, Dec 2013)

This guideline gives information to applicants wishing to register complimentary medicines for which claims of safety, quality and efficacy are being made and which have been called up for registration. It provides for implementation of Government Notice R870 of 15…

Related Tags (New Search): Complementary medicines,   Application

Complementary Medicine – Discipline-Specific Safety and Efficacy (MCC: 7.01, Jun 2016)

This guideline provides information for applicants wishing to submit applications for the registration of complimentary medicines. It includes information on the format of submission, technical details on the types of substances and preparations, naming of substances and ingredients, multicomponent formulations…

Related Tags (New Search): Complementary medicines,   Health supplements,   Ayuvedic,   Unani Tibb,   Chinese traditional,   Safety and performance,   Efficacy

Complementary Medicines – Registration Application ZA-CTD - Quality (MCC: 7.05, Jun 2016)

This guideline provides information required for the submission of an application for registration of a complimentary medicine. The guideline gives details on the administrative information, common technical document summaries and quality information required for a registration application.

Related Tags (New Search): Complementary medicines,   Health supplements,   Application

General Information: Complementary and Alternative Medicines Submissions (MCC: 9.37, Jan 2011)

General Information: Complementary and Alternative Medicines Submissions in response to Government Notice of 22nd February 2002

Related Tags (New Search): Complementary medicines

POST-MARKETING REPORTING OF ADVERSE DRUG REACTIONS TO HUMAN MEDICINES IN SOUTH AFRICA (MCC: June 2017)

Post-Marketing Reporting of Adverse Drug Reactions to Human Medicines in South Africa

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Safety,   Adverse Drug Reaction,   SRPINS,   Adverse Drug Event,   Post-marketing

Request for clarity regarding the Complementary and Alternative Medicines (CAMS) – Right of Sale Notice (GN R870 in GG 31334 of 22 August 2008)

Request for clarity regarding the Complementary and Alternative Medicines (CAMS) – Right of Sale Notice: GG Notice R.870. Please note that this is a third-party website. Juta has no control over the nature, content or availability of third-party websites, and shall…

Related Tags (New Search): Complementary medicines

Guidelines for Licence to Manufacture, Import or Export (MCC: 16.01, Feb 2004)

Recommendations for an application for a licence to manufacture, import or export medicines and medical devices. GWP guidelines apply.

Related Tags (New Search): Inspections,   GWP,   Inspections,   Complementary medicines,   MCC Inspections,   Licensing,   Application,   Fees,   Exporters,   Importers,   Manufacturers,   Medicines

Medicines and Related Substances Act 101 of 1965, Draft Regulations GG 40577, 27 January 2017

Draft regulations to the Medicines Act have been published for a comment period of 3 months. Commentary is due by the 26th April 2017. The draft regulations include the complementary medicines regulations. Medical device-specific regulations (finalised) are published…

Related Tags (New Search): Allopathic medicines,   Complementary medicines,   Health supplements,   Exporters,   Importers,   Distributor,   Manufacturers,   Community pharmacy,   Institutional pharmacy,   Regulations

Guideline Comments Form 6.13 v2, Jul 2018

Guideline Comments Form

Related Tags (New Search): Complementary medicines