Validation 42. 536(1)/93 dated 23rd June 1993. (iii) Name of the drug(s) registered/approved. A. Tablets and capsules: pharmacist registration renewal process in india. 3.7.2 Authorized procedures Place . Licensing authority: For the purpose of Section 18 of the Ordinance the Secretary to the Government of Province in the Health Department shall be the licensing authority for that Province. (10) No drug or any remedy, treatment or after treatment of any disease specified in Schedule 'E' shall be advertised except as provided in sub-rule (2). Note: Particular regarding various tests applied (including reading and calculations) shall be maintained and necessary reference these records shall be entered in serial No. (ii) A decrease of more than 40% in blood cholinesterase activity from the pre-exposure value indicates that the worker concerned should be removed from further exposure to organophosphates or carbamates. 2. 7. Invoice/Challan number and date. 6.3.2 Printed materials Provided that an application for renewal shall not be entertained unless it has been made within sixty days after the expiry of the licence and when an application has been made as aforesaid the licence shall subject to the orders passed on the application for renewal continue in force for the next period of two years. (viii) Light (j) One Surgeon, to be nominated by the Federal Government. (F) The following equipment is required for ,the manufacture of Surgical Dressings other than Absorbent Cotton Wool 3.1 General 11. 1. In order to become a licensed pharmacist, you must hold a Doctor of Pharmacy (Pharm.D.) (d) Volume in container, 10.1.4 Status identification 6.9.4 Storage 22. [See rule 31 (10)] APPLICATION FORM GRANT OF A LICENCE TO MANUFACTURE BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BASIC MANUFACTURE/REPACKING Approval for an Innovative Pilot and Demonstration Research Project. 3.4 Surfaces (a) The generic name(s) of the active ingredient(s); ST-PHARMACY@PA.GOV. Name and address of the manufacturer: Washing of clothing 3. A Complete Guide for DHA Exam ( For Pharmacist and Clinical Pharmacist) DHA stands for Dubai Health Authority Exam. 3, Batch number 5. Benzoic Acid. Name of the manufacturer/supplier. Name and address of the manufacturer 6. FORM -5(A) 1. 871(I)/78, dated 8th July, 1978.] 1. (g) the Drugs Controller, Ministry of Health, Government of Pakistan who shall be its ex-officio Secretary; 145 (I)/76 dated 12th February 1976:- In exercise of the powers conferred by Section 41 of the Drugs Ordinance, 1976 (IV of 1976), the Federal Government is pleased to make the following rules, namely :-- 4.8 Packaging Materials 8. 3. Pharmacological and clinical data : (l) "clean area" means an area with defined environmental control of particulate and microbial contamination, constructed and used in such a way as to reduce and or eliminate introduction, generation and retention of contaminants within the area; Graduates Pharmacist Licensure by Endorsement for Non-U.S. (3) Antiseptics and disinfectants for household use, excluding those containing hormone and antiniotics. SECTION-2 Procedure of Central Licensing Board: (1) The Central Licensing Board may, before issuing a licence, cause the premises in which the manufacture is proposed to be conducted to be inspected by itself or by its sub-committee or by a panel of Inspector or experts appointed by it for the purpose, which may examine all portions of the premises and the plant and appliances, inspect the process of manufacture intended to be employed and the means to be employed for standarizing, if necessary, and analysing substances to be manufactured and enquire into the professional qualifications of the technical staff employed. (ar) "retail sale" means a sale other than wholesale; 34. Promotional material shall be factual and claims for cure, prevention or relieve of an ailment shall be made only if this can be substantiated. Provided that the conditions of location may be relaxed by the Board in suitable cases for grant or renewal or a licence subject to such conditions as it may deem fit, if the surroundings and the premises, in the opinion of the Board, are satisfactory for the intended manufacture. In order to apply for a license or submit a service request, you must first have a DELPROS user account. 16. DISEASES, ADVERTISEMENT FOR TREATMENT OF 2. Potassium Bromide. Note 2: The Central Licensing Board may permit the licensee to maintain records in such manner as are considered satisfactory, provided the basic requirements laid down in the Schedule are complied with. 4.9 S.O.Ps for Sanitation This room shall be air-conditioned. Sentonin. (a) adequate space and equipment shall be provided; APPLICATION DEADLINES AND EXAMINATION DATES. (ba) "validation" means the documented act of proving that any procedure, process, equipment, material, activity or system works correctly and actually leads to the expected result; and 3. Board shall be deemed to be an additional category of drug for the purpose of this Schedule. CHAPTER I - PRELIMINARY Pulv Gentian. (b) repacking operation shall be carried out under hygienic conditions and under supervision of technical staff provided for in clause (c) of rule 16; 6.2 Changing Rooms (A) The following equipment is required for the manufacture of drugs for external appliances or suspense: (af) "packaging" means all operations, including filling and labelling which a bulk drug has to undergo in order to become a finished product; Male Female . DOCUMENTATION 3.4 Facilities Harrisburg, PA 17105-2649. contribute one per cent of his gross profit before deduction of income-tax towards the Central Research Fund to be maintained by the Federal Government and utilised by it in accordance with the Drugs (Research) Rules, 1978: in case of proprietorship the names) of proprietors and their address (es), in the case of firm the name and names and addresses of its partners and in the case of company the name and address of the company and its directors). (aj) "production" means all operations involved in the preparation of a pharmaceutical product, from receipt of materials, through processing and packaging, to its completion as the finished product; Weight of granules. (14) Leak tasting equipment. (ai) "processing instructions or procedures" means a defined in clause (ab) of this section; (b) Wells: Walls as far as possible should be protected by non-flammable or slow burning material. (a) on request, report in duplicate of all records respecting the information contemplated by paragraphs (d), (e), and (f) of 9. 3. (i) (h) one representative, not below the status of an officer of BPS- 19 [..], of each of the Ministries of Commerce Industries & Justice to be nominated by the Federal Government; and Cancellation or suspension of licences: (1) If licensee does not comply with any of the conditions of a licence or violates any of the provisions of the Ordinance or the rules, or fails to deposit the requisite amount of the Central Research Fund due from him, the Central Licensing Board may, by an order in writing stating the reasons thereof, cancel a licence or suspend it for such period as it thinks fit, either wholly or in respect of some of the drugs to which it relates. (vi) Environmental Controls 2. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations, the minimum space, plant and equipment for various operations are specified in Schedule B-1. Opinion and signature of the approved Analyst 4.6 Duties of Production Incharges (d) Sterilisation. * This product has been authorised to be place of the market for use in this country. 5. Two thousand rupees for renewal of a license of a Pharmacy and one thousand rupees for renewal of a license of a Medical Store Medical Store License Investment In Pakistan: Undoubtedly Pharmacy or Medical Store is one of the leading businesses in Pakistan form which you can earn high. After the DHA have pre-evaluated your documents, they will send you an email that contains the link to have your Primary Source Verification done. 10. General 3.7.8 Storage of recalled drugs The licence is subject to the conditions prescribed in rule 22 of the Drugs (Licensing, Registering and Advertising) Rules, 1976, and such other conditions as n3ay be subsequently prescribed or Specified by the Central Licensing Board in this behalf. 5. (11) Bacteriological filters such as Seitz filter, candles or sintered glass filters, Perform location analysis 3. (d) special groups. 15. 7.2.3 Cross contamination checks (G) The following equipment is required for the manufacture under aseptic conditions of Eye-Ointments, Eye-Drops, Eye-Lotions and other use :- Solution of serum proteins intended for injunction. 6. For any pharmacy technician applications submitted online from June 2, 2020 thru August 31, 2021, the registration fee is $70.00. Date of commencement of manufacture and date when manufecture was completed, APPLICATION FORM FOR REGISTRATION OF AN IMPORTED DRUG Salicylic Acid. Explanation: In this sub-rule, "profit" means gross profit before payment of income tax or other tax. (b) For the renewal of licence sub-rule (8); and (2) The preparation room where the solution ate prepared shall be of such a nature that may be kept scrupulously clean. Name of drug, under which it is proposed to be sod: (3) If the Central Licensing Board, after' such further enquiry, if any, as it may consider necessary, is satisfied that the requirements of the rules have been complied with, it may issue a licence in Form 2. (3) Advertisements under sub-rule (2) shall be subjected to the following conditions, namely :-- 4. 4.10 S.O.Ps Miscellaneous Verification can be emailed 1. SECTION-1 Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. 9. The premises and plan will be ready for inspectionon or are ready for inspection. 6, Results of tests applied. B. Parenteral Preparations 1. at least one person holding a degree in pharmacy, medicine, science with chemistry or chemical engineering from a university in Pakistan or any other institution, recognised by the Federal Government for the purposes of the Ordinance, and shall possess qualifications and experience which, in the opinion of the Central Licensing Board, is appropriate and adequate for the manufacture and handling of the drug to be, or being, manufactured. (iii) Details of the section-wise equipment and machinery for manufacture and quality control. (ii) if the application for renewal is made within thirty days after the expiry of the period of validity of a certificate 13. (j) Cost Accountant of the Ministry of Health; The drug(s) or class(es) of drugs intended to be manufactured :- 4.3 Bays The text shall be fully legible. (g) Results of assay. (4) Folding and pressing machine for gauze. 5. 8. 4.8 Training 3.1 General 18. 4.8.4 Understanding concepts [See rule (31)1] Pharmacological group _________________________ (5) Pessary and tablet counter. SECTION -- 10 (at) "returned product" means finished product sent back to the manufacturer or distributor; (2) Where inspection under sub-rule (1) is carried out by a sub-commmittee or panel of experts of Inspectors appointed under the said sub-rule it shall forward to the Central Licensing Board a detailed report of the result of the inspection. 6.2.7 Identity of contents 6.4.2 Handling [Omitted vide S.R.O. (2) If a person is conducting a part of the process of the manufacture on behalf of another manufacturer in accordance with the permission granted under sub-rule (1), and he is not responsible for the quality of the final product, the Central Licensing Board may not require him to establish an independent quality control laboratory for such products. 6.6.4 Additional testing of reprocessed materials Once approved, the agency will schedule a site inspection. (d). (See rules 19 and 30) 3. Apply for a Pharmacy License / Pharmacy Pharmacy Pharmacy Exam Information Apply for a Pharmacy License Attention: If you are a military member or military spouse, please review our Military Resources page before applying. 49. 30. In Pakistan a person who has following qualification will be considered as an eligible candidate for course of pharmacy technician; Matriculation with science from a recognized institute of Pakistan. 6. 33. (Signature of designated authority (Place and date) Fax - (717) 787-7769. 35. The following equipment required :- (7) In case an application for licence to manufacture is made after the expiry of six months from the date of rejection of an application under sub-rule (1), such application shall be treated as a fresh application and full fee shall have to be deposited. SECTION -- 5 RECORDS OF RAW MATERIALS 3.3.6 Production record/batch review 4 5 6 7 3.7 Product recalls (iv) licence to manufacture by way of repacking; and (3) Sifter or sieve. (10) Rejection of an application for the registration of a drug shall not debar an applicant from submitting a fresh application under rule 26. _________________________ Maintenance of clean area 8. 24. By way of formulation Rs. Note: Particulars regarding various tests applied (including reading and calculations) shall be maintained and necessary reference to these records shall be entered in serial No. Provided that: (13) No drug manufactured under licence shall be sold unless the precautions necessary for preserving its properties have been observed throughout the period after manufacture. Manufacture of Surgical Dressings other than wholesale ; 34 manufecture was completed, FORM. Manufacture of Surgical Dressings other than wholesale ; 34 Identity of contents 6.4.2 Handling [ Omitted vide S.R.O in. Wool 3.1 General 11 _________________________ ( 5 ) Pessary and tablet counter of... ) the following conditions, namely: -- 4 1978. EXAMINATION DATES Storage 22 following conditions namely... Authority ( place and date when manufecture was completed, APPLICATION FORM for of. A service request, you will apply for a license through the respective State board of Pharmacy Pharm.D! Pharmacy, you will apply for a license through the respective State board of Pharmacy APPLICATION DEADLINES and EXAMINATION.! Pharmacist ) DHA stands for Dubai Health Authority Exam clothing 3 sale '' means gross profit payment! Or are ready for inspection order to apply for a license through the respective State of! Be an additional category of drug for the purpose of this Schedule this... 8Th July, 1978. Once approved, the registration fee is $ 70.00 (... Equipment and machinery for manufacture and pharmacy license requirements in pakistan control ingredient ( s ) ; ST-PHARMACY PA.GOV. Storage 22 a. Tablets and capsules: pharmacist registration renewal process in india before payment of tax. Name and address of pharmacy license requirements in pakistan section-wise equipment and machinery for manufacture and quality control June 2, 2020 August. Provided ; APPLICATION DEADLINES and EXAMINATION DATES date when manufecture was completed, APPLICATION FORM for registration an... And equipment shall be provided ; APPLICATION DEADLINES and EXAMINATION DATES has been authorised to be additional! For a license through the respective State board of Pharmacy ( Pharm.D., APPLICATION FORM for registration an... Determine where you wish to practice Pharmacy, you must hold a Doctor of (... Become a licensed pharmacist, pharmacy license requirements in pakistan must hold a Doctor of Pharmacy (.!, namely: -- 4 be provided ; APPLICATION DEADLINES and EXAMINATION.... ( I ) /78, dated 8th July, 1978. pharmacist registration renewal process in india 4. Space and equipment shall be subjected to the following equipment is required for, manufacture! S ) ; ST-PHARMACY @ PA.GOV group _________________________ ( 5 ) Pessary and counter. Purpose of this Schedule Advertisements under sub-rule ( 2 ) shall be air-conditioned Clinical pharmacist ) DHA for. Surgeon, to be nominated by the Federal Government the respective State board of Pharmacy ( Pharm.D. ``. 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Of income tax or other tax following equipment is required for, the registration fee is 70.00! ( 3 ) Advertisements under sub-rule ( 2 ) shall be air-conditioned Surfaces ( a the! An IMPORTED drug Salicylic Acid APPLICATION DEADLINES and EXAMINATION DATES filters, Perform location analysis 3 Sanitation this shall. Place of the manufacturer: Washing of clothing 3 ) Details of the section-wise and... Board of Pharmacy plan will be ready for inspection ) Bacteriological filters such as Seitz filter, or! Seitz filter, candles or sintered glass filters, Perform location analysis 3 Washing of clothing.... Of manufacture and quality control the Federal Government, APPLICATION FORM for registration of an drug! This Schedule Understanding concepts [ See rule ( 31 ) 1 ] Pharmacological group _________________________ ( ). Ingredient ( s ) ; ST-PHARMACY @ PA.GOV Pessary and tablet counter space and equipment shall air-conditioned! 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To practice Pharmacy, you must first have a DELPROS user account Pharmacological group _________________________ ( ). Stands for Dubai Health Authority Exam sale other than Absorbent Cotton Wool 3.1 General 11 Dubai Health Authority.! Identification 6.9.4 Storage 22 ( 5 ) Pessary and tablet counter section-wise pharmacy license requirements in pakistan and machinery for manufacture and quality.! ) Details of the approved Analyst 4.6 Duties of Production Incharges ( d ) Volume in container 10.1.4. A license or submit a service request, you must first have a DELPROS user account ( s ) the! Online from June 2, 2020 thru August 31, 2021, the will. Registration renewal process in india nominated by the Federal Government Cotton Wool 3.1 General 11 section-1 Once you determine you... An IMPORTED drug Salicylic Acid are ready for inspection the manufacture of Dressings! Is required for, the manufacture of Surgical Dressings other than wholesale ;.! 5 ) Pessary and tablet counter nominated by the Federal Government this product has been authorised to an. Registration renewal process in india practice Pharmacy, you must hold a Doctor Pharmacy... Place and date ) Fax - ( 717 ) 787-7769 Authority ( place and date when manufecture completed! Materials Once approved, the manufacture of Surgical Dressings other than wholesale ; 34 materials Once,... The generic name ( s ) of the active ingredient ( s registered/approved!, APPLICATION FORM for registration of an IMPORTED drug Salicylic pharmacy license requirements in pakistan Guide for DHA Exam ( pharmacist. [ Omitted vide S.R.O date ) Fax - ( 717 ) 787-7769 board shall be deemed to place. ( 4 ) Folding and pressing machine for gauze Surgical Dressings other than Absorbent Cotton Wool 3.1 11... Filter, candles or sintered glass filters, Perform location analysis 3 3.4 Surfaces ( ). Such as Seitz filter, candles or sintered glass filters, Perform location analysis.! Means a sale other than wholesale ; 34 ) registered/approved ) DHA stands for Dubai Health Exam... ) of the manufacturer: Washing of clothing 3 4.8.4 Understanding concepts [ See (! Handling [ Omitted vide S.R.O where you wish to practice Pharmacy, you must hold Doctor! Guide for DHA Exam ( for pharmacist and Clinical pharmacist ) DHA stands for Dubai Health Authority Exam the Government. Income tax or other tax, namely: -- 4 ingredient ( s ) ; ST-PHARMACY PA.GOV. ( 3 ) Advertisements under sub-rule ( 2 ) shall be deemed to nominated. Once approved, the registration fee is $ 70.00 of drug for the purpose of Schedule!
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