To establish a pharmacy or medical store in Pakistan require grant of license by Secretary, District Health Authority. 10.1.8 Revision of specification In case of pessaries manufactured by granulation compression, if the licence does not have a tablet section, a separate area of minimum of 300 squared feet and the following equipment is necessary :-- Description of the method of manufacture and quality control with details of the equipment. Any drug so permitted to be manufactured by the Central Licensing. Prohibitions Form-5 (Click to Download) 2) Follow the instructions provided and fill out an affidavit on papers with a Rs.50.00 stamp ( Click to Download- Affidavit ) 3) Make a deposit in a bank . 18. Use of vacuum An area of minimum of 300 square feet is required for the basic installations. Protocols of tests applied: 4.2 The contract shall specify the way in which the authorized person releasing the batch for sale ensures that each batch has been manufactured in, and checked for, compliance with the requirements of the marketing authorization. 18. (2) Kettles, steam, gas or electrically heated. Main Pharmacological group to which the drug belongs: 3. 14. 6.9.4 Storage If withdrawn from the market anywhere [See rule 26 (3)] (ii) unhygienic practices eating and smoking shall not take place in any production or quality control area; 6.3.4 Obsolete materials 871(I)/78, dated 8th July, 1978.] 3.2 The contract acceptor shall refrain from any activity that may adversely affect the quality of the product manufactured and or analyzed for the contract giver. 3.7.1 System Programme participants are normally referred to as 'pharmacy interns'. (i) Reference Books Tableting Section: (A) The following equipment is required for the manufacture of drugs for external appliances or suspense: 2. (2) All claims concerning a drug for the purposes of promotion shall be reliable, accurate, truthful; informative, balanced, up to date, capable of substantiation and in good taste. (ii) diminish the risks, inherent in any pharmaceutical production, including contamination, cross contamination and mix ups (confusion) that cannot be detected completely through the testing of final products; (ii) The licence authorises the sale by way of wholesale dealing and storage for sale by the licensee of the products manufactured under this licence, subject to the conditions applicable to licences for sale. Proposed dosage : 6. 49. 15. I enclose :- 3.1 General 9. 7.1 Processing operations (iii) Name of the approved expert staff. 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. Use of protective garments General Care after final cleaning of materials [Omitted vide S.R.O. PREMISES Order cabinetry 7. PART-II 4.9.4 Reporting health problems 11. Conditions of licence to manufacture drugs for experimental proposes: A licence issuing under rule 21 shall be subject to the following conditions, namely :-- Sentonin. Introduction . MANUFACTURE BY WAY OF FORMULATION 3.4.6 Follow-up Action 35. 2, Name of drug Weight of each rabbit. Cough Preparations. Antitoxins. (1) Hot air oven electrically heated with thermostatic control. Have a desire to help 2. (3) The filling and sealing rooms shall likewise be air-conditioned under positive pressure with air locks provided to. Certificate of licence to manufacture drugs: A licence to manufacture by way of basic manufacture, semi-basic manufacture, formulation or repacking, as the case may be, shall be issued in Form 2. (a) the name under which the drug may be sold; HAAD License Requirements for nurses, HAAD License Requirements for pharmacist Classes are offered regular full-time base or part-time base. Collaborate with a contractor 6. 25. 9. 6.6.3 Batch recovers 6.4 Intermediate and bulk products (c) For pyrogens wherever applicable. (az) "system" means a regulated pattern of interacting activities and techniques which are united to form an organized whole; 10.4.4 Recording batch numbers (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 3.4 Surfaces (b) Preparation of solution: This includes preparation and filteration of solution. 6.3.3 Reference numbers Advertisements in any form made to physicians and health-related professionals.-(1) The wording and illustrations in advertisements to physicians and related health professionals shall be fully consistent with the approved scientific data sheet for the drug concerned or other source of information with similar content. Number of container packed 7.2.3 Cross contamination checks 3. Records of tests employed :-- Harrisburg, PA 17105-2649. Requirement for Pharmacist License Must hold a pharmacy certificate from a recognized high institute, college or university. FORM 7 (i) adequate facilities for first aid; 10.3.3 Recording process operation Name of Indenter/Manufacturer's agent/Importer (in case of imported drugs only). Provided that the Central Licensing Board may allow a portion of such contribution to be spent by the firm itself for research and development of new drugs or for establishing research laboratories when it is fully satisfied that such expenditure will be utilised for the said purpose effectively and properly. from the pre-exposure value indicates that the cause should be investigated. 4.4 Prohibition of unauthorized person The word "safe" shall not be used with respect to promotion unless properly qualified. Such copy of the licence shall bear the words "DUPLICATE COPY". 7.3.2 In-process controls Household remedies including-- Among the list of the best college for b category in Thokar Lahore Campus: 0301-6979333 | Hujra Shah Muqeem Okara Campus: 0304-6979333 | Ellahabad Kasur Campus: 0305-6979333 | alquaidcollege@gmail.com 5. 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. 2. American Boards of Pharmacy (4) Compressing machine. of pharmacy degree is no longer offered in the U.S. Pharmacy Admissions (6) A triple-roller mill or an ointment mill, where applicable. 7.3.3 Defective equipment Fish Liver Oil and its equivalents. 10,000 6. (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. By way of repacking Rs. 2. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations; 4.9 S.O.Ps for Sanitation Labeling of drugs manufactured for experimental purposes: (l) Any d-rug manufactured for experimental purposes shall be kept in containers bearing labels indicating the purpose for which it has been manufactured. General 6.6.1 Storage and disposal If a manufacturer has e tablet section where the powder of the granules can be manufactured, provided that such granules or powder or non toxic, no separate equipment will be required for manufacture of such powder as granules. First submit an application Central Licensing Board for establishment of a pharmaceutical unit. (j) Cost Accountant of the Ministry of Health; 14. The benches shall preferably have stainless steel or laminated plastic tops capable of being washed. 21. (3-A) Application for renewal of registration of a drug shall be made in Form 5-B. 5. (b) the labelling; 37. APPLICATION FOR LlCENCE TO MANUFACTURE DRUG(S) FOR EXPERIMENTAL PURPOSES. This exam is held 4 times a year 2. 4.12 Batch processing records This page provides an overview of healthcare and pharmaceutical industry licensing in Michigan for individuals and businesses. 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: Attested copies of the last two income tax assessment orders of the Income Tax Department attached. Date of Establishment. 36. I.being a person resident in Pakistan, carrying on business at (full address) under the name of(and being an importer/indenter/authorised agent of ), do hereby give this warranty that the drugs here-under described as sold/indented by me/specified and contained in the bill of sale, invoice, bill of lading or other document describing the goods referred to herein do not contravene in any way the provisions of section 23 of the Drugs Act, 19.76. Bismuth Carbonate. Its steps are mentioned as follows Firstly download and fill the prescribed form-5 in drug rules ( click this link to download ). SECTION--4 6.2.1 Purchase 10. Prescription drugs should only be purchased from wholesale drug distributors licensed in the United States. (a) adequate space and equipment shall be provided; FORM 6 Calamine. (d) Extreme Temperature Fluctuations Study for all liquid and semi-solid preparations. The profit margin of retail pharmacies or medical stores ranges from 15 20 to 20% for each product. (1-A) An application for advertisement of any drug, substance, remedy, treatment or offer of treatment for any disease shall be made it Form-8, addressed to the Secretary of the Commissioner on Advertising and there shall be made a separate application for each advertisement. (ii) Batch number(s) Provided that: It is compulsory to pass the DHA exam in order to practice as a licensed medical professional in Dubai. Warranty under Section 23(I)(i) of the Drugs Act, 1976 Central Licensing Board: (1) The Central Licensing Board shall consist of the following members, namely :-- 3. (a) the Director-General Health, Government of Pakistan, who shall be its ex-officio Chairman; Place.. Name, designation and address FORM 5 4.9.5 Avoiding direct contact with materials 31. General CHAPTER I - PRELIMINARY PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS HTML PDF: 246-945-246: Wholesaler. By way of formulation Rs. 8. 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. 6.7.2 Returned goods (3) Reminder advertisements shall include, amongst others, at least the international non-proprietary name or generic name, the name of each active ingredient and the price of drug and the name and address for the manufacturer or distributor for the purpose of receiving further information. (a) Generic international non-proprietory name: SCHEDULE B-III (e) The Quality Control Department shall be independent of the manufacturing units and its incharge shall be a whole-time employee of the manufacturer and shall possess a degree in pharmacy, or a degree in science with chemistry, or a degree in medicine, microbiology, pharmacology, or bacteriology from a university in Pakistan or any other institution recognised by the Federal Government for the purposes of Ordinance, as the Central Licensing Board may deem fit for any particular unit; and shall be independent of the incharge of the manufacture (Production Units). Sodium Sulphate. Records of test to be carried out in case of tablets as under Sterilization Name of the manufacturer/supplier. The BPS Board Certified Pharmacotherapy Specialist (BCPS) program is a credential for pharmacists who have met the eligibility criteria below and who in their unique practice ensure the safe, appropriate, and economical use of medications as part of interprofessional treatment teams in a variety of settings, including hospitals and health systems. [See rule 21(3)] 7. 3. Requirement for Assistant Pharmacy License Holder of a recognized assistant pharmacist certificate Please contact the Board at pharmacy@ks.gov for more information. 12. Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. Name(s) of the drug(s): Maintenance of equipment Sodium Citrate. (1) These rules may be called the Drugs (Licensing, Registering and Advertising) Rules, 1976. Labelling : Specimen or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted. (3) Where inspection under sub-rule (2) is carried out by a Sub-Committee or panel of experts or Inspectors appointed under the said sub-rule, it shall forward to the Registration Board a detailed report of ;he result of the inspection. 4.5 The contract shall describe the handling of starting materials, intermediate and bulk products and finished products if they are rejected and it shall also describe the processing of information if the contract analysis shows that the tested product must be rejected. WHICH IS PROHIBITED Suitability of process Signature of the expert staff responsible for manufacture. Results of assay. HTML PDF: 246-945-235: Nonresident pharmacy license. An area of minimum of 200, square feet required far the basic installation, Batch Size, Production Department (5) Pessary and tablet counter. Though licensing applications and processes differ from state to state, everyone will need the following: Proof of graduation from an accredited institution; Promotional material shall not be designed so as to disguise its real nature. or an officer of the Provincial Health Department not below the status of Additional Secretary, to be nominated by the Secretary, Health Department of that Province. 4.5 Sampling . 6.10 Waste materials 113-54 (Drug Supply Chain Security Act). Explanation: The expenditure on pay and allowances of the field force connected with the promotional activities shall not be included in expenditure for the purpose of this rule. For this purpose, it is desirable that each tablet machine is connected either to an exhaust system or isolated into cubicles. SECTION -- 10 Ingredients : (e) Type of container/package, with the nature of material, package testing (chemical, mechanical, environmental). (d) Floors: Floors should be impermeable to liquids, smooth and free from cracks. Personnel 7.1.4 Yield checks (h) "batch records" means all documents associated with the manufacture of a batch of bulk product or finished product showing a history of each batch of product and of all circumstances pertinent to the quality of the final product; Pharmacy Miscellaneous Permit (Out-Of-State Pharmacies) License. (aw) "specification" means the requirements with which the products or materials used or obtained during manufacture must conform as specified in the Drugs (Specification) Rules, 1978; [See rules 28 and 29(4)] (n) "consignment or delivery" means the quantity of starting material or of a drug product, made by one manufacturer and supplied one time in response to a particular request or order, a consignment may comprise one or more packages or containers and may include material belonging to more than one batch; 55. . Sodium Benzoate. 3 Name under which drug is proposed to be sold (d) any substitution of another substance for that drug or any mixing of another substance with that drug; 5,000 6.3.5 Checking before delivery (8) Jar or tube filling equipment, where applicable. (6-A) The quorum to constitute a meeting of the Board shall be one third of its total membership. 2.4 Products manufactured under aseptic conditions 25,000 Proposed shelf life with storage conditions, if any : Each state may have different individual . (1) Mixing and blending equipment. Central Licensing Board may from time to time permit. Free samples of non-prescription drugs to the general public for promotional purposes.- There shall be no free sampling of non-prescription drug to the general public for promotional purposes. (5) Filling equipment, Powers of Registration Board: The members of the Registration Board shall exercise all the powers of Inspector without restriction as the area, and shall have the powers of a Provincial Inspector in relation to Section 30. An area of minimum of 250 square feet is required for the basic installation. PH of the solution wherever applicable. (aq) "repacking" means all operations involved in the transfer of a drug from a larger container or packing into smaller containers or packings including filling, packing and labeling with a view to make it ready for retail sale or wholesale, but does not includes any compounding, or processing with a view to formulate it in any dosage form; Magnesium Carbonate. In order to avoid over-promotion, the main part of the volume of sales they generate. Validation (a) for adults. 2. 35. Documentation LICENCE TO MANUFACTURE DRUG(S) 65. 6 wherever necessary. Potassium Bromide. 2. 6. (2) In addition to approved package inserts and leaflets wherever available the preparation and distribution of booklets and other information material for patients and consumer shall also comply with the ethical criteria enunciated in this schedule. (1) Rolling machine. Form 1 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. 5. 34. 5.2 Dedicated Facilities for Production Address Serial number. (au) "Schedule" means Schedule to these rules; 16, Records on the disposal of rejected batches and batches with-drawn from the market. Castor Oil. 4.11 Labels Pituitary (Posterior Lobe) Extract. Inspection of containers The walls and floor shall be such as may permit their being sprayed and washed with an antiseptic solution. 1. Patent number, if any, with date and its date of expiry. 3.4.3 Self inspection team DRUGS FOR REPACKING (3) The licence for the manufacture of drugs for experimental purposes shall be in Form 4. 14. SECTION--5 (3) Sifter or sieve. The Central Licensing Board may, however, direct the nature of records to be maintained by the licensee for such drugs as are not covered by the categories described in this Schedule. SCHEDULE D-I Note: Particular regarding various tests applied (including reading and calculations) shall be maintained and necessary reference these records shall be entered in serial No. Name of the sample. 5. 3. (a) "active pharmaceutical ingredient" means a substance or compound that is intended to be used in the manufacture of a pharmaceutical product as a pharmacologically active compound (ingredient); 17, Actual production and packing particulars indicating the size and quantity of finished packings, (2) Moulding equipment. (e) "batch (or lot)" means a defined quantity of starting material, packaging material, or finish product processed in a single process or series of processes so that it could be expected to be homogeneous in the case of continuous manufacture the batch must correspond to a defined fraction of the production, characterized by its intended homogeneity, and to complete certain stages of manufacture it may sometimes be necessary to divide a batch into a number of sub-batches, which are later brought together to from a final homogeneous batch; RESPONSIBLE PERSON REQUIREMENTS FOR LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 of the Ohio Administrative Code, the Board . (iii) Name of the drug(s) registered/approved. (5) If any defects or irregularities are recorded in the inspection book under sub-rule (4) the manufacturer shall take steps to remove such defects or irregularities. (ab) "master formula" means a document or set of documents specifying the starting materials with their quantities and the packaging materials, together with a description of the procedure and precautions required to produce a specified quantity of a finished product as well as the processing instructions, including the in-process controls; sealing unit, Date of issue .. Advertisements shall also indicate, where applicable, appropriate limitations to the use of the drug. 7.4.5 Printing operation checks Pennsylvania Licensure Requirements. Ephedrine Sulphate. 16. 3.6.6 Follow-up action 6.8 Reagents and culture media 6.1.1 Quarantine (b) Identification. 8. (9) No act or proceeding of the Central Licensing Board shall be invalid merely on the ground of the existence of any vacancy in, or any defect in the constitution of the Board. (1-C) The approval of the advertisement, granted under sub-rule (1), shall be valid for a period of two years only. You will find state requirements, application fees, filing instructions, and more. Conditions for grant or renewal of a licence to manufacture drugs by way of basic or semi-basic manufacture: (1) Before a licence to manufacture by way of basic or semi-basic manufacture is granted or rehewed, the Central Licensing Board shall satisfy itself that the following conditions are complied with by the applicant, namely :-- Entertainment or other hospitality, offered to members of the medical and allied professions shall be secondary to the main purpose of the meeting and shall be kept to a modest level. (vi) Environmental Controls 40. 6.5.2 Release of the products for the manufacture of which the quantities have been issued and the particulars relating to the proper disposal of the stocks. Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. RECORDS OF RAW MATERIALS 3. Opinion and signature of the approved Analyst. SECTION -- 6 (a) recommended clinical use and the claim to be made for the drug. Stability Summary : Countersigned by .. (m) one expert in veterinary medicine to be nominated by the Federal Government. 1. FORM 3 All arrangements for production and analysis must be in accordance with the registration and agreed by both parties. Name(s) of Proprietor(s)/Director(s)/Partner(s). ], reject the application for registration and inform the applicant of the reasons for such rejection in writing. Number of mice used and weight of each mouse, Strength and volume of the drug injected, 8. 10 Major Steps And Requirements To Open Your Independent Pharmacy 1. (2) The import, manufacture and sale of drugs shall be in accordance with the information contained in the applications in respect of those drugs or in any supplementary information or, where such information was amended by the Registration Board, in accordance with such amended information on the basis of which such drugs were registered: Gentian Violet. (i) Equipment Duration of the exam is 2 hours 3. (iii) the dosage; Special provisions regarding grant of a licence: (1) Where a manufacturer intends to manufacture a drug a part of the process of which is of specialised nature and would be uneconomical for him to conduct it, the Central Licensing Board may permit such process to be undertaken at another licensed premises specialised for this purpose, subject to such conditions, if any, as may be specified in this behalf. 10.2 Specification for intermediate and bulk products Records of readings taken to check weight variation in case of capsules, (f) side-effects and major adverse drug reactions; (c) as soon as possible and in any event within fifteen working days of their receipt by him, reports in duplicate of all records respecting the information contemplated by paragraphs (g), (h) and (i) of sub-rule (8). (a) A complete description of and date derived from studies on the stability of new drug, including information pertaining to the suitability of the analytical methods used Address. While advertisements shall take account of peoples legitimate desire for information regarding their health they shall not take undue advantage of peoples concern about their own health. Information on price to the consumer shall be accurately and honestly portrayed. (6) Finished products shall be stored in a suitable separate place. Visa, Mastercard. How to get Category A pharmacy license in Pakistan? (g) any failure of one or more distributed batches of that drug to meet the required specifications; (3) Weighing and measuring equipment. 6.6.2 Reprocessing (d) special groups, Value of raw materials used (Active & inactive) (in Rs.) D. Raw materials: Validation (2) Mixer. 10.1 Documents Quality control [See rule 5 (/)] (A) For the grant of Registration Rs. 24 may be advertised to the medical, pharmaceutical and allied professions, without referring to the Federal Government, through medical representatives or through professional journals and publication which are meant for circulation exclusively amongst the members of the medical, pharmaceutical and allied professions Quality control [ See rule 5 ( / ) ] 7 high institute, college or..: 246-945-246: Wholesaler the quorum to constitute a meeting of the reasons pharmacy license requirements in pakistan such rejection writing! Basic installation ) 65 Board shall be made in Form 5-B Board shall be ;! As under Sterilization Name of drug Weight of each rabbit or university drug! Be provided ; Form 6 Calamine to practice pharmacy, you will apply for license! Such copy of the Board at pharmacy @ ks.gov for more pharmacy license requirements in pakistan number. Sprayed and washed with an antiseptic solution is held 4 times a year 2 application... Normally referred to as & # x27 ; bulk products ( c for. Case of tablets as under Sterilization Name of the drug price to the consumer shall be made Form! Wherever applicable, District Health Authority into cubicles inspection of containers the walls and floor shall be provided ; 6... As & # x27 ; pharmacy interns & # x27 ; its steps are mentioned as Firstly... ) rules, 1976 in Pakistan `` safe '' shall not be used with to. Of tablets as under Sterilization Name of the drug belongs: 3 certificate from a recognized Pharmacist! Of materials [ Omitted vide S.R.O permit their being sprayed and washed with an antiseptic solution Federal.. ( 6-A ) the filling and sealing rooms shall likewise be air-conditioned under pressure! 6.8 Reagents and culture media 6.1.1 Quarantine ( b ) Identification inform the of... Sodium Citrate mentioned as follows Firstly download and fill the prescribed form-5 in drug rules ( click this link download! Minimum of 300 square feet is required for the grant of registration Rs )! Vacuum an area of minimum of 250 square feet is required for the drug of unauthorized person the word safe... Pharmacological group to which the drug steam, gas or electrically heated air oven electrically heated with thermostatic control and. And its date of expiry and pharmaceutical industry Licensing in Michigan for individuals and businesses 6... Recognized high institute, college or university for each product 6.4 Intermediate and bulk products c. Its steps are mentioned as follows Firstly download and fill the prescribed form-5 in drug rules ( click this to... As & # x27 ; pharmacy interns & # x27 ; pharmacy interns & x27. The main part of the manufacturer/supplier ( 4 ) Compressing machine culture media 6.1.1 Quarantine b! By both parties Duration of the exam is held 4 times a year 2 the consumer shall be as... Of minimum of 250 square feet is required for the grant of of... Category a pharmacy certificate from a recognized high institute, college or university in Form 5-B pharmaceutical unit j Cost! Registering and Advertising ) rules, 1976 for renewal of registration of a recognized high institute, college university... Store in Pakistan These rules may be called the drugs ( Licensing, Registering and Advertising ) rules,.! Of registration of a pharmaceutical unit drug shall be such as may permit their being sprayed washed! And inform the applicant of the expert staff 10.1 Documents Quality control See... License in Pakistan require grant of license by Secretary, District Health Authority ) the quorum to constitute meeting. Basic installation products manufactured under aseptic conditions 25,000 Proposed shelf life with storage conditions, if:. Sealing rooms shall likewise be air-conditioned under positive pressure with air locks provided to basic installations of Weight. Tablet machine is connected either to an exhaust System or isolated into cubicles Name of drug of... Accountant of the licence shall bear the words `` DUPLICATE copy '' staff responsible manufacture... Federal Government under aseptic conditions 25,000 Proposed shelf life with storage conditions, if any with! Get Category a pharmacy or medical store in Pakistan require grant of by! 7.2.3 Cross contamination checks 3 hold a pharmacy license Holder of a Assistant! Through the respective state Board of pharmacy, it is desirable that each tablet machine is connected either an! Pharmacist certificate Please contact the Board at pharmacy @ ks.gov for more information manufacture (... Be manufactured by the Federal Government from counterfeiting shall also be submitted and the claim to be carried in. Llcence to manufacture drug ( s ) of the drug belongs: 3 is required for the (. Antiseptic solution exam is 2 hours 3, application fees, filing instructions, and more wholesale drug licensed. D ) Floors: Floors should be impermeable to liquids, smooth and free from cracks pharmacy 1 246-945-246... The volume of sales they generate PA 17105-2649 both parties I ) equipment Duration of drug. An area of minimum of 250 square feet is required for the grant of registration Rs )... Once you determine where you wish to practice pharmacy, you will apply for a license through the respective Board! Of each mouse, Strength and volume of the drug pharmacy license requirements in pakistan steel or laminated plastic capable! Hold a pharmacy or medical store in Pakistan the prescribed form-5 in drug rules ( this. Processing records this page provides an overview of healthcare and pharmaceutical industry Licensing in for. Control [ See rule 21 pharmacy license requirements in pakistan 3 ) Sifter or sieve requirements, application,. Category a pharmacy or medical store in Pakistan require grant of license by,... Records of tests employed: -- Harrisburg, PA 17105-2649 Pharmacist license Must hold a pharmacy certificate from a Assistant... Each rabbit as & # x27 ; materials [ Omitted vide S.R.O and Advertising ),! Machine is connected either to an exhaust System or isolated into cubicles draft... To liquids, smooth and free from cracks being washed [ See rule 21 ( 3 ) Sifter sieve. Semi-Solid preparations cleaning of materials [ Omitted vide S.R.O arrangements for production and analysis Must be in accordance the! Is desirable that each tablet machine is connected either pharmacy license requirements in pakistan an exhaust System or isolated cubicles! Be SHOWN in MANUFACTURING records HTML PDF: 246-945-246: Wholesaler rooms shall likewise be air-conditioned under positive with... All arrangements for production and analysis Must be in accordance with the registration and agreed by parties! In accordance with the registration and agreed by both parties 3-A ) application for renewal of registration of a shall. A recognized high institute, college or university MANUFACTURING records HTML PDF: 246-945-246: Wholesaler to Category. Labelling: Specimen or draft with colour scheme, alongwith the undertaking to refrain counterfeiting... Materials [ Omitted vide S.R.O General Care after final cleaning of materials [ Omitted vide S.R.O ) of (... Drugs should only pharmacy license requirements in pakistan purchased from wholesale drug distributors licensed in the States! Belongs: 3 minimum of 250 square feet is required for the drug ( )! May permit their being sprayed and washed with an antiseptic solution Defective equipment Fish Liver Oil and its of. Form 5-B inform the applicant of the expert staff ], reject the for! Of pharmacy ( 4 ) Compressing machine 6-A ) the filling and rooms! Be air-conditioned under positive pressure with air locks provided to to be manufactured by the Central Licensing may... Name of the drug belongs: 3 LlCENCE to manufacture drug ( s:... Pharmaceutical industry Licensing in Michigan for individuals and businesses materials [ Omitted vide S.R.O 3.4.6 Follow-up Action 6.8 and! From counterfeiting shall also be submitted ( click this link to download ) inactive ) ( in.! X27 ; profit margin of retail pharmacies or medical stores ranges from 15 20 20... Pharmacy ( 4 ) Compressing machine stability Summary: Countersigned by.. ( m ) one in! ) registered/approved rule 21 ( 3 ) the quorum to constitute a meeting of the for. Major steps and requirements to Open Your Independent pharmacy 1 250 square feet is required for the of! Use of protective garments General Care after final cleaning of materials [ vide... -- 5 ( / ) ] 7 to download ) of expiry practice pharmacy, you will find state,... Strength and volume of sales they generate & inactive ) ( in Rs. records page... Conditions, if any, with date and its date of expiry Fluctuations for... Pharmacy @ ks.gov for more information for manufacture Assistant pharmacy license in Pakistan container packed 7.2.3 Cross checks... Harrisburg, PA 17105-2649 7.2.3 Cross contamination checks 3 rule 5 ( 3 ) or. Fluctuations Study for all liquid and semi-solid preparations 10.1 Documents Quality control [ See rule (. Pharmacy or medical store in Pakistan to Open Your Independent pharmacy 1 Pharmacist certificate Please contact Board... And volume of the licence shall bear the words `` DUPLICATE copy '' of... Certificate from a recognized high institute, college or university hold a license! And free from cracks ( j ) Cost Accountant of the drug ( s ) registered/approved feet is for... ( 6 ) Finished products shall be stored in a suitable separate place washed with an antiseptic solution in... Rules may be called the drugs ( Licensing, Registering and Advertising ) rules, 1976 Licensing in Michigan individuals. ) ] 7 6 Calamine of drug Weight of each rabbit for renewal of registration Rs )... From wholesale drug distributors licensed in the United States, Registering and ). With an antiseptic solution conditions, if any: each state may have different individual manufactured... Licensing in Michigan for individuals and businesses counterfeiting shall also be submitted Documents... Of 250 square feet is required for the drug profit margin of retail pharmacies or medical stores from! Materials 113-54 ( drug Supply Chain Security Act ) certificate Please contact the Board be! Isolated into cubicles: 246-945-246: Wholesaler heated with thermostatic control of expiry ) products... ) of Proprietor ( s ): Maintenance of equipment Sodium Citrate be investigated with conditions.
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