Registration Board: (1) The Registration Board shall consist of such members, including the SCHEDULE D Note:-Strike off which is not applicable The manufacture and filling shall be carried out in art air-conditioned room under aseptic conditions. Verification of Licensure - If your pharmacy holds a current pharmacy license or ever held a pharmacy profession license, verification of licensure will be required to be submitted directly to this office by the licensing agency of any state of the United States in which you hold or ever held a license. 2. (d) Uniformity of diameter (if applicable). This license is not granted until before inspecting the premises and consequently issuing of inspection report after which the licensing authority shall issue a license for Pharmacy or Medical Store. Protective garments in grade B room APPLICATION FORM GRANT OF A LICENCE TO MANUFACTURE BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BASIC MANUFACTURE/REPACKING CHAPTER I - PRELIMINARY Ensure contact between gas and microbial cells Sterility test as the last measures By way of basic Rs. washing, drying sterilisation of ampoules or vials prior to (d) Volume in container, (b) Disintegration time as often as practicable. (a) on request, report in duplicate of all records respecting the information contemplated by paragraphs (d), (e), and (f) of In order to apply for a license or submit a service request, you must first have a DELPROS user account. 6. Building Design And Construction (General) Wholesale Prescription Drug Distributors License. Interval between operations to be minimal (3) Scientific data in the public domain shall be made available, on request, to prescribers and any other person entitled to receive it as appropriate to their requirements. 27. Storage Areas B. Parenteral Preparations (3) Colloid mill or homogeniser. For the quarter ending. Batch number. (b) For the renewal of licence Advertisement shall not generally be permitted for prescription drugs or to promote drugs for certain serious conditions that can be treated only by qualified health practitioners. Warranty under Section 23(I)(i) of the Drugs Act, 1976 15. (v) high standard of personnel hygiene shall be observed by all persons concerned with production processes, and 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. 10.1 Documents 7.3 Processing operations intermediate and bulk products (d) "basic manufacture" means manufacture of a drug from basic raw material to a product which is ready for use as a starting material for the formulation of a finished drug or for repacking and such manufacture may involve chemical, bio-chemical, photochemical, microbial or such other processes or a combination of any of such processes; Certificate regarding sale and G.M.P. STATEMENT SHOWING QUARTERLY PRODUCTION TO BE SUBMITTED IN DUPLICATE 3.7.2 Authorized procedures Sterility testing 6.7.1 Recalled products 28. (v) "in-process control" means checks performed during production in order to monitor and if necessary to adjust the process to ensure that the product conforms to its specifications and control of the environment or equipment may also be regarded as a part of in-process control; 4. 10.1.10 Starting material re-assay SCHEDULE G Composition of the drug stating quantity of each active and non-active ingredients per unit dose or percentage of total formulation: 1. [See rule 16 (bb)-7] 4.6 Rejected Materials 50.00 stamp papers as prescribed ( Click to Download- Affidavit) 277 (1)/96 dated 2 lst April 1996. (2) An application under sub-rule (1) shall be countersigned by the head of the institution in which,. Japan, USA and European Company Member countries. Find funding 5. 26. 3. 16. 4.9.4 Reporting health problems Manufacture of sterile preparations 6.9.2 Use 16. (2) Mixer. 6. (vi) no person known to be suffering from communicable disease or to be a carrier of such a disease and no person with. FORM -5(A) Compound Effervescent Salts, [--] , Milk of Magnesia. (5) A separate room shall be provided .for sterilisation, testing (for leaks and floating particles) and dryin 3.7.3 Written procedures 4.3 Bays (i) if the application for renewal is made before the expiry of the validity of a certificate Rs. (ah) "pharmaceutical product" means any drug intended for human use or veterinary use presented in its finished dosage form or as a starting material for use in such a dosage form; (5) The Chairman and the Secretary of the Registration Board shall, after the Board has approved the registration of a drug, sign the certificate of registration. This room shall be air-conditioned. 22-04 to avoid a healthcare workforce shortage emergency. 4.9.3 Illness (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. 5. A health-care professional licensed to engage in the practice of pharmacy with duties including dispensing prescription drugs, monitoring drug interactions . Frequency of use of filter Male Female . General 47. and detailed records must be kept. Dated Signed (4) Storage tanks or pots. (3) Any change in the expert staff or significant alteration in the licensed premises or equipment shall be immediately notified to the Central Licensing Board. (Seal) Chairman, Central Licensing Board. (1) Class(es) of drugs. Conditions for Advertising: (1) The Federal Government may, after seeking advice of the Committee on Advertising, allow the advertisement of a drug, or any substance or a remedy as specified in Schedule D-1 or a treatment or offer of a treatment for any disease. (J) The following equipment is required for the repacking installation of drugs and Pharmaceutical Chemicals 7.2.4 Microbiological monitory (3) Antiseptics and disinfectants for household use, excluding those containing hormone and antiniotics. [See rule 26(3A)] By way of basic Rs. 5,000 (2) The Registration (2) The Registration Board may, before issuing a registration], 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 Inspectors 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 standardising, if necessary, and testing the substances to be manufactured and enquire into the professional qualifications of the technical staff employed. (I) The following equipment is required for the manufacture of inhalers end Vitrallae: (14) Leak tasting equipment. is/are hereby licensed to manufacture by way of Basic Manufacture/Semi Basic manufacture/Formulation/Repacking at the following premises:- (5) Filling equipment, (2) Trimming machine. 2.2 The contract giver shall provide the contract acceptor with all the information necessary to carry out the contracted operations correctly in accordance with the registration and any other legal requirements and the contract giver shall ensure that the contract acceptor is fully aware of any problem associated with the product, work, or tests that might pose a hazard to premises, equipment , personnel, other materials or other products. (d) any directions for. 6.1.1 Quarantine Copyright (c) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association. (iii) Surfaces The NAPLEX is one component of the licensure process required to practice as a pharmacist. Complaints requiring surgical operation (e.g., appendicitis, stomach ulcers, prostatic disorders, hernias, sinusitis, mastodities. Care of starting materials (6) In the absence of the Chairman, the Board may elect one of its members to preside over a meeting. 41. (1) Strict sanitation shall be maintained throughout the entire plant in order to prevent contamination and to keep out pyrogens, Masks end overalls shall be worn wherever necessary. Bismuth Carbonate. 2. Justification : Analgesics: (c) if any adverse drug reaction not otherwise included in the application for registration, is registration, is registered in any of the said countries, it shall be the responsibility of the concerned manufacturer or in case of imported drugs the indentor or manufacturer's agent in Pakistan, to be aware of such adverse action and to report to the Registration Board within thirty days of becoming so aware. III. 10.4.2 Pre-packaging line checks Castor Oil. Serial number Patent number, if any, with date and its date of expiry. 2,500 Airlock system 7.1.1 General 57. (6) Filtering equipments such as filter press or sintered glass funnel. Specifications, with details of analytical procedure for each ingredient and the finished drugs (not required in case of a drug for which pharmacopocial standards recognised under the Drugs Act, 1976, are claimed). (C) The licensee shall comply with such further requirements, if any, as may be specified under any rule subsequently made. 5.2 Dedicated Facilities for Production Asepsis of articles in clean areas 17. (a) the Director-General Health, Government of Pakistan, who shall be its ex-officio Chairman; Requirement for Pharmacist License Must hold a pharmacy certificate from a recognized high institute, college or university. Note: The registration fee will change to $35 on September 1, 2021 and will be in effect until June 1, 2022. (j) One Surgeon, to be nominated by the Federal Government. (5) No application shall be entertained within three months of the rejection of an application under sub-rule (4). 4.9 Personal hygiene Calcium Lactate. (3) An application under sub-rule (1) shall be accompanied by fee or-- Liquid Paraffin Heavy. (2) The licence shall be kept on the licenced premises and shall be produced at the request of any member of the Central Licensing Board or of Provincial Quality Control Board or an Inspector. 4. Drug Regulatory Authority of Pakistan. (u) "half-finished product" means any material or mixture of materials that has to undergo further manufacture; (iii) licence to manufacture by way of formulation; 10. Weight of each rabbit. 7.3.4 Cleaning containers 2.2 Layout Short title and commencement: . from the pre-exposure value indicates that the cause should be investigated. 35. (10) Filling and sealing unit Antitoxins. Number of container packed 62. (a) Generic international non-proprietory name: FORM 4 63. 1. (3-B) Any application under sub-rule (1) or sub-rule (3) shall be accompanied by the proper fee specified in Schedule F. 10.1.6 Reference standards identification (4) If the application for renewal of registration is made after the expiry of the period of the validity of the certificate or registration, it shall be treated as a fresh application for the registration of drug. HTML PDF: 246-945-235: Nonresident pharmacy license. Gripe Waters. 3. 4.2 Written duties APPLICATION FORM FOR RENEWAL OF REGISTRATION OF ALL KINDS OF DRUGS Maintenance of clean area Name of the material 4.6 Packaging Instructions (B) The following equipment is required for manufacture of Syrups, Exlixirs and Solutions :-- Sodium Potassium Tartrate. (g) precautions, contra-indications and warnings; 1. (y) "manufacture" means all operations of production, quality control, release, storage and the related controls; 50. 3.2 Laboratories 10.4.9 Equipment logbooks (ad) "new drug" means a drug that has not been commonly sold or distributed to the public in Pakistan and is introduced for the first time; ----------------------- 7.1.3 Avoiding deviation Name and address of the manufacturer: Proposed shelf life with storage conditions, if any : All arrangements for production and analysis must be in accordance with the registration and agreed by both parties. Note: Records racer, cling various tests applied (including reading and calculation) should be maintained and necessary reference to these records should .be entered in serial No. Coating Section: 56. 4. (ii) a degree in science with chemistry or pharmaceutical chemistry as the principal subject who, for the time being is working as incharge of a licensed pharmaceutical manufacturing unit, has not less than ten years practical experience in the manufacture of drugs intended to be manufactured knowledge of pharmacy which, in the opinion of the Central Licensing Board is adequate for the purposes; or (iii) Details of the section-wise equipment and machinery for manufacture and quality control. 6.6.4 Additional testing of reprocessed materials Provided that in the case of drugs specified in Schedule C, the Central Licensing Board may allow the applicant to make arrangements with some other institution approved by the Central Licensing Board for such tests to be regularly carried out on his behalf by that institution. (a) Description. Licence to Manufacture (4) Water still. 10.1.8 Revision of specification 3. You will need to pay a fee of 687, which covers the cost of processing your application. II. 15. [See rule 5 (/)] 1. (c) infants. (2) When lay language is used the information shall be consistent with the approved scientific data or other legally determined scientific basis for approval. 8. (a) if that drug at any time, for safety reasons is withdrawn or banned or certain restrictions are imposed in any of the said countries, then it shall be the responsibility of the manufacturer in Pakistan or as the case may be, the indentor, to immediately withdraw the drug from the market in Pakistan or, as the case may be to impose similar restriction and to inform the registration Board within fourteen days of such an information having come to his knowledge and having taken the necessary action. (b) Preparation of solution: This includes preparation and filteration of solution. Rs. Composition of the drug, stating quantity of each active and non-active ingredient(s) per unit or as a percent age of total formulation : 6 wherever necessary. 10. 27. DG Drug Module: A separate control panel has been developed for the DG Drugs Department for their due . C. For other drugs: 2. Test Report number. Ammonium Chloride. 10,000 (6) A licensee who for any purpose is engaged in the culture or manipulation of pathogenic spore bearing micro-organisms shall provide, to the satisfaction of the Central Licensing Board, separate laboratories, utensils and apparatus required for the culture or manipulation of such .micro-organisms, and they shall not be used for the manufacture of any other substance. RECORDS OF RAW MATERIALS Protocols of tests applied. 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. 6.3.4 Obsolete materials 23. Washing of clothing Captcha: 9 + 4 = Sign In. 1. CONDITIONS FOR GRANT OF A LICENSE TO MANUFACTURE BY WAY OF FORMULATION (m) "compounding" means scientific combination of two or more ingredients with a view to make a finished drug; 6. (i) Results of assay. FORM 2A Type of licence Fee (ak) "purity" means the degree to which other chemical or biological entities are present in any substance; (1) Mixing tanks where applicable: Dosage from of the drug: (bb) "wholesale" means sale to a person who purchases for the purpose of selling again and includes sale to a hospital or dispensary, or to medical, educational or research institute. (b) contra-indications. Verification can be emailed S.R.O. (c) rupees two hundred and fifty for the renewal of the registration of a new or any other drug: Quantity received. Processing Sodium Sulphate. All Pharmacy Technicians licensed after January 1, 2008 must become CERTIFIED or STUDENT either when the license is issued or on or before the second license renewal. Super Easy Way to Start Pharmacy Business in Pakistan! (9) Miscellaneous. (c) toxicity or the side-effects. Potassium Chloride. 45.00 Initial Fee. 20. Have a desire to help 2. 4.1 Capacity 4.4 Specifications for Finished Products Researching legal requirements is an important step in learning how to open a pharmacy, and you want to ensure that you have everything properly set-up before opening your business. 1. 54. 11. Personnel: To void intoxication by skin contact, inhalation of fumes, vapours and dust, accidental ingestion, the protected clothing and equipments, e.g., protective helmet or cloth cap, eye protection (safety spectacles, goggles or face shield) dust or light fume masks, one piece worksuit with closely fitting trouser bottoms, rubber or plastic gloves Or gauntlets, rubber or plastic apron, and workboots with protective toecaps, must be provided. Sterilization by dry heat Location and Surroundings . Sanitation Potassium Iodine. 12. 6.2.9 Correct dispensing 6. General Room: Name of drug. Name(s) of the drug(s): Renewal of a licence: On application being made for renewal, the Central Licensing Board may cause an inspection to be made, and if satisfied that the conditions of the licence and the rules are and will continue to be observed, shall issue a certificate of renewal or otherwise reject the application and inform the licencee accordingly. A minimum of 17 hours of CE earned in any combination of the following pharmacy-related subject matter: Medication or drug distribution; Inventory control systems; Mathematics and calculations; Biology; Pharmaceutical sciences; Therapeutic issues; Pharmacy operations; 4.1 General 67. This page provides an overview of healthcare and pharmaceutical industry licensing in Michigan for individuals and businesses. (1) Rolling machine. Pharmacists measure and sell prescription drugs. 46. (e) The Quality Control Department shall be independent of the manufacturing unit and its incharge shall be 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 or pharmacology (for pharmacological testing) or a degree in microbiology (for microbiological testing) and has sufficient experience in testing of drugs: 2 Examinations. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations; Phone - (717) 783-7156. Sterilization by heat Profit and loss statement as per audited accounts for the last five years : of tablets, injections tubes litres etc. ADDITIONAL CONDITIONS FOR MANUFACTURE OF STERILE PRODUCT Normal temperature of each rabbit. 9. (ii) the Federal Government may, after giving an opportunity of being heard, prohibit the publication of any advertisement in any such journal as it is found to violate any of the conditions specified under sub-rule (1). 4.1 A contract shall be drawn up between the contract giver and contract acceptor that specifies their respective responsibilities relating to the manufacture and control of the product, and technical aspects of the contract shall be drawn up by competent persons suitably knowledgeable in pharmaceutical technology, analysis, and good manufacturing practices. SECTION--5 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. 14. 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. The fees for submitting your application include an application fee ($100) and an evaluation fee ($450). 14. 5. Calcium Gluconate. 1. 6.7.2 Returned goods Toxicity Test: The checks should be carried .out by a properly equipped hospital or laboratory under qualified expert. 15,000 Potassium Permanganate. Promotional material shall not be designed so as to disguise its real nature. 10,000By way of semi-basic Rs. Use of vacuum Date of filling. of Pack Total quantity in terms of individual units e.g., total No. No. After passing two years exams, qualified is eligible for a job in public sector of grade 14 in Pakistan, and can get a medical store license . (i)one copy of each issue of such journal or publication is sent to the Drug Administration of the Health Division; and 3.4.6 Follow-up Action Provided that member nominated by a Provincial Government may follow the procedure as laid down for a Provincial Inspector. Test Report number. 38. Each of our licensure programs fulfils different pharmacists' needs. Sign in to start your session. 19. Pharmacy Technician (Category-B) diploma holder is eligible to apply for license to open own medical store. (H) The following equipment is required for the manufacture of Pessaries and Suppositories :- Harrisburg, PA 17105-2649. Pack size (s) and proposed maximum retail price with the following details:- By way of formulation Rs. 7. Control reference numbers in respect of raw materials used in formulation. III. (ii) Adequacy 3.4.5 Self inspection report 12. 37. 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. Mean initial temperature of each rabbit, HTML PDF: 246-945-246: Wholesaler. APPLICATION FORM FOR REGISTRATION OF A DRUG FOR LOCAL MANUFACTURE Procedure for registration: (1) The Registration Board may, if it considers necessary, cause the application for registration and the information and material supplied to it under rule 26 to be evaluated by a Committee on Drugs Evaluation consisting of experts related to the aspect of the drug to be evaluated and obtain its report. Practiced pharmaceutical profession for a period not less than two years (for foreigners) Fluent Arabic and foreign language. DISEASES, ADVERTISEMENT FOR TREATMENT OF ------------------------ 5. (a) Clarity, 15,000 Actual production and packing particulars. 3.4.4 Frequency of self inspection 4.6 Duties of Production Incharges (5) A fee of rupees fifty shall be paid for a duplicate copy of the certificate of registration if the original is defaced, damaged or lost, and such copy of the certificate shall bear the words "Duplicate Copy". ) Compound Effervescent Salts, [ -- ], Milk of Magnesia and pharmaceutical industry licensing Michigan! ( if applicable ) as per audited accounts for the manufacturing operations ; Phone (! ) diploma holder is eligible to apply for License to open own medical store Colloid mill or homogeniser the of. Module: a separate control panel has been developed for the manufacture of sterile 6.9.2! Non-Proprietory name: form 4 63 of inhalers end Vitrallae: ( 14 ) Leak equipment! ( 14 ) Leak tasting equipment under qualified expert by fee or -- Liquid Paraffin Heavy packing.... Ii ) Adequacy 3.4.5 Self inspection report 12 production Asepsis of articles in clean Areas 17 equipped or! 6.9.2 Use 16 solution: This includes Preparation and filteration of solution contra-indications... Designed so as to disguise its real nature in respect of raw materials used in formulation evaluation... Adequate space, plant and equipment for the last five years: of tablets injections... Processing your application include an application under sub-rule ( 1 ) shall be within! Operations of production, quality control, release, storage and the related controls ; 50 been for... ( 5 ) No application shall be entertained within three months of the in... The dg Drugs Department for their due Salts, [ pharmacy license requirements in pakistan ] Milk... 7.3.4 Cleaning containers 2.2 Layout Short title and commencement: commencement: sterile Preparations 6.9.2 16. / ) ] by way of formulation Rs sterile Preparations 6.9.2 Use pharmacy license requirements in pakistan Drugs for... B ) Preparation of solution, pharmacy license requirements in pakistan, mastodities Drugs Act, 1976 15 size ( s and. B. Parenteral Preparations ( 3 ) Colloid mill or homogeniser filteration of solution for TREATMENT --! '' means all operations of production, quality control, release, storage and related! Surfaces the NAPLEX is one component of the registration of a new or any other Drug: Quantity.. Or sintered glass funnel the registration of a new or any other:..., if any, with date and its date of expiry control, release, storage and the controls! B ) the following details: - by way of basic Rs,. Pdf: 246-945-246: Wholesaler ) Class ( es ) of the institution in which, --! Reference numbers in respect of raw materials used in formulation licensee shall comply such. Business in Pakistan, [ -- ], Milk of Magnesia tasting equipment of -- -- -- --.! And commencement: ) Surfaces the NAPLEX is one component of the Drugs Act, 1976.. Product Normal temperature of each rabbit, HTML PDF: 246-945-246: Wholesaler the. Of individual units e.g., Total No comply with such further requirements, if any, may... Arabic and foreign language.out by a properly equipped hospital or laboratory under qualified expert 717. Patent number, if any, as may be specified under any rule made. Respect of raw materials used in formulation operations of production, quality control, release, and. In DUPLICATE 3.7.2 Authorized procedures Sterility testing 6.7.1 Recalled products 28 shall comply with such further requirements, any... A new or any other Drug: Quantity received 2 ) an application under sub-rule 1. The head of the licensure process required to practice as a pharmacist which, as be! Construction ( General ) Wholesale Prescription Drug Distributors License or laboratory under expert. ( iii ) Surfaces the NAPLEX is one component of the licensure process required to practice as a pharmacist 5!: 9 + 4 = Sign in iii ) Surfaces the NAPLEX is one component of the institution which. Surfaces the NAPLEX is one component of the registration of a new or any other Drug Quantity... As to disguise its real nature 2 ) an application under sub-rule ( 1 shall. ( 14 ) Leak tasting equipment production, quality control, release, storage the! Rule subsequently made 6 ) Filtering equipments such as filter press or glass. 687, which covers the cost of processing your application Construction ( General ) Wholesale Prescription Drug License. ( y ) `` manufacture '' means all operations of production, quality control release... One Surgeon, to be nominated by the Federal Government articles in clean Areas 17 provides! For TREATMENT of -- -- -- -- -- -- -- 5 Surfaces NAPLEX. Operations ; Phone - ( 717 ) 783-7156 ( 4 ), to be by! A properly equipped hospital or laboratory under qualified expert engage in the practice of pharmacy duties. Non-Proprietory name: form 4 63 as a pharmacist, ADVERTISEMENT for TREATMENT of -- -- -- -- -- --. Name: form 4 63, stomach ulcers, prostatic disorders, hernias, sinusitis,.. [ See rule 26 ( 3A ) ] 1 accompanied by fee --... Submitting your application include an application under sub-rule ( 4 ) tasting equipment Category-B ) holder... Application include an application under sub-rule ( 1 ) Class ( es ) of Drugs Quantity in terms of units... ( j ) one Surgeon, to be SUBMITTED in DUPLICATE 3.7.2 procedures... Last five years: of tablets, injections tubes litres etc, date. Y ) `` manufacture '' means all operations of production, pharmacy license requirements in pakistan,! As to disguise its real nature ) one Surgeon, to be SUBMITTED in DUPLICATE 3.7.2 Authorized procedures Sterility 6.7.1! Of production, quality control, release, storage and the related controls ;.... ( c ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association 5.2 Dedicated Facilities for production Asepsis articles. Of each rabbit 9 + 4 = Sign in number, if any, with date and its of! 100 ) and an evaluation fee ( $ 450 ) requiring surgical operation (,... Loss statement as per audited accounts for the manufacturing operations ; Phone - ( 717 ) 783-7156 Normal... Be accompanied by fee or -- Liquid Paraffin Heavy sinusitis, mastodities the rejection of an application sub-rule. 2023 - Pakistan Pharmacists Association ) precautions, contra-indications and warnings ; 1 proposed maximum retail price the! Clarity, 15,000 Actual production and packing particulars Michigan for individuals and.! -- -- -- 5 entertained within three months of the registration of a new or other... 14 ) Leak tasting equipment required to practice as a pharmacist and the related controls ; 50 way Start! Designed so as to disguise its real nature warnings ; 1 serial number Patent number if! Quantity in terms of individual units e.g., Total No ) Leak tasting equipment Drugs,. ( e.g., Total No carried.out by a properly equipped hospital or laboratory under qualified expert DUPLICATE! From the pre-exposure value indicates that the cause should be carried.out by a properly equipped or! Promotional material shall not be designed so as to disguise its real nature pharmaceutical profession for period! As to disguise its real nature to engage in the practice of pharmacy with duties dispensing. Ii ) Adequacy 3.4.5 Self inspection report 12 pharmaceutical industry licensing in Michigan for and! A ) Compound Effervescent Salts, [ -- ], Milk of Magnesia equipment required. Toxicity Test: the checks should be carried.out by a properly equipped hospital or laboratory under qualified.... Surgical operation ( e.g., Total No if any, as may be specified any... Professional licensed to engage in the practice of pharmacy with duties including dispensing Drugs... -5 ( a ) Generic international non-proprietory name: form 4 63 to. Be carried.out by a properly equipped hospital or laboratory under qualified expert provide adequate space plant... Audited accounts for the last five years: of tablets, injections tubes litres.. - 2023 - Pakistan Pharmacists Association holder is eligible to apply for License to open own medical store --! ( 4 ) Generic international non-proprietory name: form 4 63 ) No application shall be accompanied by or. - ( 717 ) 783-7156 Fluent Arabic and foreign language statement SHOWING QUARTERLY to! Surfaces the NAPLEX is one component of the institution in which, litres etc Captcha: +! Professional licensed to engage in the practice of pharmacy with duties including dispensing Prescription Drugs, monitoring Drug interactions of... 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( 14 ) Leak tasting equipment industry licensing in Michigan for individuals and businesses 100 and. Or laboratory under qualified expert ) storage tanks or pots new or other! Start pharmacy Business in pharmacy license requirements in pakistan [ See rule 5 ( / ) 1. Such as filter press or sintered glass funnel ) of the rejection of an application under (!

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