licences to manufacture or wholesale medicines

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Subsidiary Legislations for the Regulation of Chinese Medicines sale and manufacture of Chinese medicines Formed in accordance with the Ordinance in September 1999 the Council is responsible for formulation and implementation of the regulatory measures The Ordinance stipulates that all traders engaging in the retail and wholesale of Chinese herbal medicines and in the manufacture and medicines and poisons and generally for the control and regulation of the profession of pharmacy in Malawi and for matters incidental to or connected therewith [15TH JANUARY 1991] PART I PRELIMINARY [Ch3501s1]1 Short title This Act may be cited as the Pharmacy Medicines and Poisons Act [Ch3501s2]2 Interpretation

Eudra GMP

Manufacturing and Importation Authorisation: Manufacture of medicinal products in the EU or importation from a third country is subject to the holding of a Manufacturing and Importation Authorisation The National Competent Authority of the Member State in which the manufacturer or importer operates issues these authorisations

Queensland Department of Health has granted Schedule 4 and Schedule 8 licences This will enable the company to manufacture and wholesale S8 and S4 drugs including medical cannabis Production validation will be completed by the end of the December and

Companies that are involved in the manufacture or supply of medicines in the UK need to have the relevant licence for the activity in question Medicines regulation now extends to the entire supply chain for medicinal product and imposes rigorous standards on medicines manufacturers and wholesale dealers who trade in them as well as brokers who negotiate sales The regulation of licensing of

Medicines Poisons and Therapeutic Goods Bill 2013 Contents Part 1 — Preliminary 1 Authorisation of pharmacists to manufacture medicines or use or possess Schedule 7 poisons 27 27 Part 4 — Licences permits and notices Division 1 — Licences and permits 34 Licences 33

Chapter 6 and the Medicines Poisons and Therapeutic Goods Regulation 2008 at part 18 2 for a manufacturers licence and at part 18 4 for a suppliers licence If granted a licence will confer the following authorisations and responsibilities on the licence holder and to other persons authorised under the licence

TAMIL NADU FOOD SAFETY DRUGS ADMINISTRATION

Form 24C - Application for the grant or renewal of a licence to manufacture for sale [or for distribution] of Homoeopathic medicines or a licence to manufacture potentised preparations from back potencies by licensees holding licence in Form 20-C Download Now 10

MEDICINES ACT 2003 Arrangement of Articles 1 Short title and commencement PART I Manufacture of Medicinal Products for Human Use 37 39 Granting of manufacturer's licences 40 Notice for further information A 201 41 Suspension or revocation of a manufacturer's licence 42 Inspection in relation to manufacturer etc 43 Duration

no manufacturing licences are required (HMRs Part1 Reg 3) Similarly where medicines are prepared under the supervision of a pharmacist and in accordance with exemptions in the retained section 10 of the 1968 Act (chapter 3) no licences are required (HMRs Part1 Reg 4) Classificationofmedicines

Chinese Medicine Council chairman Daniel Tse said today everyone engaged in the retail or wholesale business of Chinese herbal medicines and manufacture or wholesale of proprietary Chinese medicines must apply for licences from the Council's Chinese Medicines Board

LICENCES AND CERTIFICATES RELATING TO MEDICINAL PRODUCTS 4 Licensing authority 5 General provisions as to dealing with medicinal products 6 Provisions as to manufacture and wholesale dealing 7 Exemptions for pharmacists and practitioners 8 Exemption in respect of herbal remedies 9 General exemptions

These Regulations made under the Medicines Act 1968 relate to applications for the grant of manufacturer's licences and wholesale dealer's licences other than licences of right They prescribe the form and manner in which such applications are to be made and specify the information that shall accompany each application

These Regulations made under the Medicines Act 1968 relate to applications for the grant of manufacturer's licences and wholesale dealer's licences other than licences of right They prescribe the form and manner in which such applications are to be made and specify the information that shall accompany each application

The Pharmacy and Poisons (Manufacturers Licensing) Committee issues licences to manufacture pharmaceutical products or revokes or suspends any of them for a specified period as it thinks fit in accordance with regulation 29 of the Pharmacy and Poisons Regulations (Cap 138A Laws of

Procedure for Issue of Retail and Wholesale Drug License

licences Blood Bank surgical and medical device units To carry out inspection of manufacturing process of sera/ vaccines units To monitor and issue GMP GLP certificates including issuance of MSC NVC COPP Free sales certificate etc Approval of Quality control laboratory of medicines

16 Offences relating to manufacture supply use and possession of Schedule 7 poisons 18 17 Offences relating to manufacture supply use and possession of Schedule 9 poisons 19 18 Offences relating to supply and use of strictly controlled substances 19 19 Use of poison obtained under permit 21 20 Unlawfully obtaining poison by wholesale 21

Medicines and Poisons Regulations 2016 Contents As at 30 Jan 2017 Version 00-a0-02 page v Extract from see that website for further information 72 Purposes for licence or permit for Schedule 9 poison 55 73 Information to be recorded in register for licences and permits 55 Division 2 — Licences 74 Types of licence 56 75

Wholesale dealer's licence 4 No person shall engage in the wholesale distribution of medicinal products unless he is in possession of a wholesale dealer's licence hereinafter referred to as the licence to that effect Registering of activity with the Authority 5 (1) Distributors of active substances who are established in

An application for an import License shall be made to the licensing authority in Form 8 for drugs excluding Schedule X and in Form 8-A for Schedule X drugs either by the Manufacturer or by the Manufacturer's agent in India who is having the wholesale license for sale or distribution of drugs and shall be accompanied by a License fee of one thousand rupees for a single drug and one hundred

The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe MHRA was formed in 2003 with the merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA)

Other safety alerts : The United Kingdom: Notice: Medicines: terminated and cancelled manufacturing and wholesale dealer licences : The MHRA issues a notice on a list of companies in the UK who have their licence to manufacture or wholesale medicines terminated and cancelled

inside the State for the importation storage and wholesale distribution of medicines 13- "Pharmaceutical Factory" means the production unit inside the State whose divisions cooperate to manufacture the medicine or pharmaceutical preparation 14- "Scientific Offices" means the scientific centres that provide

Unlawfully obtaining poison by wholesale 21 21 Fraudulent behaviour to obtain supply of poison 22 22 Storage handling transport and disposal of poisons 22 23 Record keeping and reporting 23 24 Vending machines 23 Medicines and Poisons Act 2014 Contents page ii [This compilation shows amendments proposed by Bill No 139-1 (Pt 11 Div 5) ] Part 3 — Authorisation of health professionals

REGISTRATION AND LICENSING REQUIREMENTS *Licences to manufacture import or export or act as a wholesaler to wholesale and or distribute medicines are issued in accordance with the requirements of Section 22C read with Regulation 19 of the Medicines and Related Substances Act 1965 (Act 101 of 1965) *Licences for the manufacturer of Cannabis who is not exempted from the

Medicines and Poisons Regulations 2016 Contents As at 30 Jan 2017 Version 00-a0-02 page v Extract from see that website for further information 72 Purposes for licence or permit for Schedule 9 poison 55 73 Information to be recorded in register for licences and permits 55 Division 2 — Licences 74 Types of licence 56 75

14-12-1992wholesale prescription drug industry will be promoted by requiring the A wholesale prescription drug distributor license Manufacturer Any entity engaged in manufacturing preparing propagating compounding pharmacies to place a direct order of medicine from the pharmaceutical manufacturer (2)