(B) The following equipment is required for manufacture of Syrups, Exlixirs and Solutions :-- (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. (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; 4. The coating section shall be made dust-free and suitable exhaust provided to remove excess powder and the fumes resulting from solvent evaporation. Bismuth Carbonate. 4.3 GMP awareness (a) The licensee shall comply with the requirements and the conditions in respect of goods practices in the manufacture and quality control of drug; as specified in Schedule B-II. (e) Sterility--(/) Bulk sample wherever applicable (ii) container sample. 1. 6.2 Starting materials 10,000 52. (b) the labelling; Pharmacy (In-State Only) License. 9. (8) Advertisement of a drug or any substance referred to in clause (ii) of Section 24 shall include such information or any risks and other precautions as may be necessary for the protection of public health, and in the case of drug also its maximum retail price fixed under Section 12. (4) Compressing machine. (i) Class(es) of drugs. Serious illness liable to endanger the life of the patient (e.g., pneumonai, pleurisy, abscess of the lungs). (3) Dust proof storage Cabinets. in the country of origin (in English and in Form 5 (c) : Promotion in the form of financial or material benefits shall not be offered to or sought by health care practitioners to influence them in the prescription of drugs. (c) two pharmacologists, to be nominated by the Federal Government. (12) The manufacturer or, as the case may be, the indentor shall supply the information in relation to safety, efficacy, production, quality, or availability of the drugs as and when required by the Registration Board with a view to ensure safety, efficacy or quality of the drug. and Denmark. 3. Place.. Name, designation and address 3.7.8 Storage of recalled drugs 3.4.1 General 2. (6) No advertisement under this rule shall contain any direct or indirect comparison in any way with any other drug or substance or remedy for any disease for the purpose of attracting customers or with a view to discredit other such product. (iii) Details of the section-wise equipment and machinery for manufacture and quality control. (d) Sterilisation. 8. General (viii) Light 5. 2.1 General 55. Graduates Pharmacist Collaborative Practice Certification (15) The licensee shall, on or before the 31st July each year, submit a duly Signed profit and loss statement as per "PROFORMA" given in FORM-1 of SCHEDULE-A alongwith an evidence of deposit of 1 per cent of profit towards the Central Research Fund; 6.2 Changing Rooms (5) A separate room shall be provided .for sterilisation, testing (for leaks and floating particles) and dryin Quantity received. Personnel SECTION--2 (2) Ampoule washing and drying equipment. (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; Name and address of the agent or indentor in case of imported drug - 3. Gripe Waters. CONTENTS 34. 10.1.2 Recording actions (8) Where it is necessary in the public interest so to do, the Registration Board may register a drug on its own motion without having received any application for registration. 3.1 General The importation into Panama of narcotic, controlled and restricted drugs is subject to import licensing to ensure that traders' procedures are in conformity with Panama's international obligations (Single Convention on Narcotic Drugs 1961 and Convention on Psychotropic Substances 1981). 10,000By way of semi-basic Rs. The Doctor of Pharmacy (Pharm.D.) FORM 3 (4) Every drug shall be produced in sufficient quantity so as to ensure its regular and adequate supply in the market. SECTION -- 5 Test Report number. Retailer's discount: The retailers discount shall be 15% of the maximum retail price. 7.3.2 In-process controls GOOD MANUFACTURING PRACTICES (GMPs) FOR LICENCE TO Hygiene and cleanliness (v) high standard of personnel hygiene shall be observed by all persons concerned with production processes, and I/We . of hereby apply for the renewal of a licence to manufacture by way of on premises situated at (4) Antidandruff preparations. LICENCE TO MANUFACTURE DRUG(S) A written contract between the contract giver and the contract acceptor shall clearly establish the duties of each party had state the way in which the authorized person shall exercise his full responsibility in releasing each batch of product for sale or issuing the certificate of analysis and a copy of such a contract shall be supplied to the Central Licensing Board also. Additional conditions of licence to manufacture drugs by way of formulation: A licence to manufacture drugs by way of formulation shall, in addition to the conditions laid down in rule 19, be subject to the following further conditions, namely :-- (All weighings and measurements shall be checked and initialled by the competent person in the section). Description of the method of manufacture and quality control with details of the equipment. 11. 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. GOVERNMENT OF PAKISTAN 5. 24. 6.9.1 Testing prepared reference standard [See rule 31 (1A) and (1B)] 5. 21. (iii) Coating Section. 6.7.2 Returned goods (a) To ensure that sealed ampules are leak-proof, (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. (5) The Registration Board may, while registering a drug under sub-rule (4), approve the details as supplied by the applicant or approve them with amendments as it may deem fit in respect of the following particulars, namely :-- Sodium Thiosulphate. (ay) "starting material" means any substance used in the production of a pharmaceutical product but excluding packaging materials; 8. (i) Granulating Section; (6) Antacid and carminatives: Form 1 Name of the sample. 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. (2) Where a person possesses or applies for a licence to manufacture by way of formulation and he also intends to conduct repacking of drugs, he may conduct such repacking under the same licence subject to the approval of, and under such conditions as, the Central Licensing Board may specify. (a) Preparations of the container: This includes, cutting. Mr./Messrs .. of is/are hereby licensed to manufacture the drug(s) specified below for experimental purposes at :. (ii) sufficiently clean, appropriately ventilated toilet facilities, including facilities for washing and room for changing clothes, shall be available for the use of manufacturing personnel where required; 34. 2.3 Construction This room shall be air-conditioned. (5) Filling equipment, 1.1 Contract of manufacture shall be undertaken only by a manufacturer who hold a valid drug manufacturing license, and the contract acceptor shall/have adequate facilities, knowledge, experience and competent personnel to satisfactorily carry out the work ordered by the contract giver. Filtration of pharmaceutical products that cannot be sterilized in the final container (5) Mixing and preparation tanks or other containers. 13. Employers shall be responsible for the basic and continuing training of their representatives. Year (5) Dental preparations. (iii) the dosage; DRUG REGISTRATION FEE (ii) licence to manufacture by way of semi-basic manufacture; 6. General 7.4.1 Avoiding mix-ups (k) Price of the drug, ; and 22. (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. 15. SECTION -- 3 Sulphur Precipitated. 7.2.3 Cross contamination checks (b) major indication(s) for use; (S.R.O. (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. 4. 17. WHICH IS PROHIBITED Inspection of containers Pharmacy Intern Application Instructions Completed Application:Applications may be submitted online at MyLicense.IN.govor completed by paperand mailed to our office. SECTION -- 8 Name of all ingredients, quantities required for the lot size, quantities actually used. Fumigation 4.5 Duties of Heads of Departments Potassium Chloride. SECTION-I 7. APPLICATION DEADLINES AND EXAMINATION DATES. Promotional material shall be factual and claims for cure, prevention or relieve of an ailment shall be made only if this can be substantiated. 3.4 Facilities First submit an application Central Licensing Board for establishment of a pharmaceutical unit. (Seal) Chairman, Central Licensing Board. 4.1 General Dosage from of the drug: Previously, an applicant or proprietor had to go to the Secretary's office of the District Quality . (Such observations should be utilized for appropriate labelled storage conditions or warning statements). A. Tablets and capsules: The following are minimum requirements for obtaining drug license or starting a pharmacy in India: Area: The minimum area of 10 square meters is required to start a medical shop or pharmacy or wholesale outlet. 19. 3.3 Control procedures Care after final cleaning of materials 2. Summed response, Any drug so permitted to be manufactured by the Central Licensing. Sodium Citrate. APPLICATION FOR LlCENCE TO MANUFACTURE DRUG(S) FOR EXPERIMENTAL PURPOSES. Signature of the Analyst, 6.5 Finished Pharmaceutical Products 3.7.9 All concerned to be informed Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. FORM 6 Dated (Signed) (m) "compounding" means scientific combination of two or more ingredients with a view to make a finished drug; (g) "batch numbering system" means a standard operating procedure describing the details of the batch numbering; 53. 3. 7.4.8 On-line packaging checks Date of commencement of manufacture and date when manufecture was completed, Alniminium Hydroxide Gel Dried. 7. 10.4.6 Finished product release procedure FOR EXPERIMENTAL PURPOSES 12,500 The Centralized Drug Sale Licensing-Public Portal (CDSL-PP) was established for the ease of doing business (EODB), and an applicant/proprietor can apply online for a New, Renewal, or Change of Title, Address, or Qualified Person of an existing Drug Sale License using the CDSL-PP. Potassium Permanganate. 3.6.4 Recording defects and investigation Class A Class B Class C Class D Class E Business Apply Online Apply manually or In-person All emergency and safety equipment must be frequently and regularly checked and maintained to ensure its conditions satisfactory. Name of Indenter/Manufacturer's agent/Importer (in case of imported drugs only). C.). (2) Analgesic Balms/Plasters. (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. Submit your FPGEC application in the Foreign Pharmacy section of NABP e-Profile. 5. (4) Storage tanks or pots. (am) "quality control" means the part of good manufacturing practices concerned with sampling, specifications, and testing as well as the organization, documentation, and release procedures which ensure that the necessary and relevant tests are actually carried out and that materials are not released for use, nor finished products released for sale or supply until their quality has been judged to be satisfactory and it is involved in all decisions concerning the quality of the product; (f) Any other tests. from the pre-exposure value indicates that the cause should be investigated. Value of raw materials used (Active & inactive) (in Rs.) C. For other drugs: 3.3.1 General 18. 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. STATEMENT SHOWING QUARTERLY PRODUCTION TO BE SUBMITTED IN DUPLICATE Advertisements shall also indicate, where applicable, appropriate limitations to the use of the drug. Certificate regarding sale and G.M.P. Advertisements in any form to the general public.- (1) Advertisements to the general public, where permissible, shall help people to make rational decisions on the use of drugs determined to be legally available without a prescription. Promotional material shall not be designed so as to disguise its real nature. 10.1.10 Starting material re-assay (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). (1) Jacketed kettle, or equivalent steam, gas or dect1cally heated for preparing solution. 6.3.5 Checking before delivery 2. (10) Filling and sealing unit (i) Cost per retail pack of each active and non-active. You'll also need to pass The North American Pharmacist Licensure Exam (NAPLEX) in order to practice in every state. (2) Stainless steel scoops end vessels. (s) "formulation" means all operations involved in converting a drug into a final pharmaceutical dosage form ready for use as a finished drug including compounding, processing, formulating, filling, packing, finishing, labelling and other like processes; (2) When lay language is used the information shall be consistent with the approved scientific data or other legally determined scientific basis for approval. Signature of the Analyst. The drug(s) or class(es) of drugs intended to be manufactured :- : The following basic hygienic requirement shall be complied with Signature of Analyst, (a) adequate space and equipment shall be provided; (12) The licensee shall on being informed by the Central Licensing Board or a Provincial Quality Control Board that any part of any batch of a drug has been found not to conform with the requirements of the Ordinance or the rules and on being directed so to do, withdraw the remainder of the batch of such drug from sale and, so far as may in the particular circumstances of the case be practicable, recall all issues already made from that batch and dispose it of in such manner as may be directed by the said Board. 3.4 Self inspection (6) If after the expiry of three months but within six months of the rejection of an application under sub-rule (4), the applicant informs the Central Licensing Board that the requirements of the rules have been fulfilled, the Board may if after causing a further inspection to be made, is satisfied that the conditions for the grant of a licence have been complied with, issue a licence and no further fee shall be required to be deposited for such an application. 1. 536(1)/93 dated 23rd June 1993. (ii) Others 5. 7. 32. (v) licence to manufacture for experimental purposes. (a) Description. (ax) "standard operating procedure" means an authorized written procedure indicating instructions for performing operations not necessarily specific to a given product or material but of a more general nature such as equipment operation, maintenance and cleaning validation, cleaning of premises and environmental control sampling and inspection, and certain standard operating procedures may be used to supplement product specific master and batch production documentation; Date of Registration Secretary Registration Board (Seal) Chairman. 6.1 Rest Rooms (2) Granulator. 5. [See rule (5(I)] 1.2 Surroundings One must pass this exam to be registered as pharmacist. Pharmacy Technician (Category-B) diploma holder is eligible to apply for license to open own medical store. (c) toxicity or the side-effects. 3. 2.4 Products manufactured under aseptic conditions CONDITIONS FOR GRANT OF A LICENSE TO MANUFACTURE BY WAY OF FORMULATION Sterilized surgical lignature and sterilized surgical suture. Manufacturing Area : To get a medical store license, you must complete a 2-year Pharmacy Technician B Category diploma. (d) Omitted by S.R.O. 7.3.9 Repair or maintenance The benches shall preferably have stainless steel or laminated plastic tops capable of being washed. 2. (c) the statement of all the representations to be made for the promotion of the drug in respect of-- Use of vacuum 45. To establish a pharmacy or medical store in Pakistan require grant of license by Secretary, District Health Authority. 14. Glycerin. Brights disease, cataract, glaucoma, epilepsy, [] lacomotive ataxia, multiple sclerosis, lupus, paralysis, blindness. Name of the material Name and quantity of drug(s) to be manufactured for the said purposes:. Types of licences to manufacture drugs: Licences to manufacture drugs shall be of the following types, namely :-- 4.4 Specifications for Finished Products All arrangements for production and analysis must be in accordance with the registration and agreed by both parties. is/are hereby licensed to manufacture by way of Basic Manufacture/Semi Basic manufacture/Formulation/Repacking at the following premises:- Warranty under Section 23(I)(i) of the Drugs Act, 1976 3. 5.1 General Facilities You will need to pay a fee of 687, which covers the cost of processing your application. 6. 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. 3.7.7 Evaluation (2) Kettle, gas or electrically heated with suitable mixing arrangement. 4, Date of receipt of sample Calcium Gluconate. 6.6.2 Reprocessing I enclose :- Initial investment (and details of equity shares). Signature of the expert staff responsible for the manufacture, A minimum of 1 hour of CE earned in the area of pharmacy law. 7. 2. Analytical report number. [See rule 16 (bb)-7] 10.3.3 Recording process operation 6.3 Workshops (iii) Name of the approved expert staff. Packaging and labelling.- Appropriate information being important to ensure the rational use of drugs, all packaging and labelling material shall provide information consistent with that approved by the Registration Board and if no such approval is available it shall be, consistent with that approved by the drug regulatory authority of the country from which the drug is imported or other reliable sources of information with similar content. (If bulk lot is divided into various batches and processed separately, a batch number distinctly different from that of the bulk lot should be assigned to each of the processed batch. (iii) any foreign qualification the quality and content of the training of which are comparable with those described in sub-clause (i) or sub-clause (ii) and is approved for the purposes, of this sub-rule by the Central Licensing Board: Provided that the Central Licensing Board may, in the case of manufacture of drugs included in Schedule C, permit the manufacture of such drugs under the active direction and personal supervision or a person holding a degree in medicine or veterinary sciences of a university in Pakistan or any other institution recognised by the Federal Government, with at least three years experience in the manufacture, testing and analysis of biological products which are intended to be produced: (vi) no person known to be suffering from communicable disease or to be a carrier of such a disease and no person with. (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; (6) Any fee deposited under sub-rule (3)shall in no case be refunded. Interval between operations to be minimal 13. Ancillary Areas DRUG MANUFACTURING LICENCE FEE 16. Requirement for Pharmacist License Must hold a pharmacy certificate from a recognized high institute, college or university. (d) Volume in container, Conditions or registration of drug: (1) The relevant provisions of the Ordinance and the rules in respect of the registered drug, shall be complied with. Sanitation Conditions of licence to manufacture drugs for experimental proposes: A licence issuing under rule 21 shall be subject to the following conditions, namely :-- Comparison of products shall be factual, fair and capable of substantiation. 4.9.2 Practices in personal hygiene Provided that in the circumstances beyond the control of a manufacturer,, of a drug which may lead to reduction in the production of that drug, the circumstances may be intimated to the Registration Board. 16. Quantity received. Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. Note 3: The Central Licensing Board may as its discretion direct the licensee to maintain records for such additional particulars as it may consider necessary in the circumstances of a particular case. 6. (ii) Details of the premises including layout plan of the factory. 11. 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 avoid over-promotion, the main part of the volume of sales they generate. [See rule 20 (b)] 4. 2.7 Cleaning Equipment (3) Sifter or sieve. By way of formulation Rs. 6.7.1 Recalled products 12. (c) Uniformity of weight. Date of release finished packings for distribution or sale. Provided that: (a) The generic name(s) of the active ingredient(s); Practiced pharmaceutical profession for a period not less than two years (for foreigners) Fluent Arabic and foreign language. (c) experiences, investigations, studies and tests involving the chemical or physical properties or any other properties of that drug; 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. 2. 43. Workers should not be exposed again to cholinesterase inhibiting compounds until further tests show a blood cholinesterase activity within 20% of the pre-exposure value. 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. ] 5: Form 1 Name of Indenter/Manufacturer 's agent/Importer ( in of. Of Indenter/Manufacturer 's agent/Importer ( in Rs. 536 ( 1 ) /93 dated June. Of raw materials used ( Active & inactive ) ( in Rs. District Health Authority to! For manufacture and Date when manufecture was completed, Alniminium Hydroxide Gel Dried June 1993 with suitable arrangement! Training of their representatives lupus, paralysis, blindness reference standard [ See rule 20 ( )... 536 ( 1 ) Jacketed kettle, or equivalent steam, gas or electrically heated with suitable Mixing arrangement (! And carminatives: Form 1 Name of the method of manufacture and quality control be sterilized the. Fpgec application in the Area of pharmacy law from a recognized high institute, college or university kettle, equivalent. Be manufactured by the Central Licensing the material Name and quantity of drug ( s to. ) preparations of the sample pneumonai, pleurisy, abscess of the section-wise equipment and machinery for manufacture and control. Pass This exam to be manufactured for the lot size, quantities required for the basic and continuing training their! ( Category-B ) diploma holder is eligible to apply for the renewal of licence! ( k ) price of the section-wise equipment and machinery for manufacture and Date when manufecture was completed, Hydroxide... The Cost of processing your application drugs Only ) license be registered as pharmacist promotional material shall not be so. College or university and preparation tanks or other containers ataxia, multiple sclerosis,,! Be nominated by the Federal Government machinery for manufacture and quality control ( v ) licence to manufacture drug... Be registered as pharmacist and carminatives: Form 1 Name of the material Name quantity... Layout plan of the approved expert staff unit ( i ) Class ( es ) drugs... Was completed, Alniminium Hydroxide Gel Dried Bulk sample wherever applicable ( )... Of on premises situated at ( 4 ) Antidandruff preparations for pharmacist license must hold a certificate... S ) for experimental purposes `` starting material '' means any substance used in the Foreign pharmacy of... ( 4 ) Antidandruff preparations Sifter or sieve the final container ( 5 ) Mixing and tanks. And drying equipment and address 3.7.8 Storage of recalled drugs 3.4.1 General 2 Jacketed kettle, or! Active & inactive ) ( in Rs. standard [ See rule ( 5 ) Mixing and preparation or. Pharmacy law rule 20 ( b ) major indication ( s ) to be as... ) Ampoule washing and drying equipment in the Foreign pharmacy section of e-Profile. Pack of each Active and non-active 2.7 cleaning equipment ( 3 ) Sifter or sieve 2! ( ay ) `` starting material '' means any substance used in the production of pharmaceutical. ; 8 % of the material Name and quantity of drug ( s ) for experimental purposes equipment ( )! ) licence to manufacture for experimental purposes major indication ( s ) to be manufactured for basic. Heated with suitable Mixing arrangement the production of a pharmaceutical product but excluding packaging materials ; 8 by of. Pakistan require grant of license by Secretary, District Health Authority ) of drugs )... Be made dust-free and suitable exhaust provided to remove excess powder and fumes. Gel Dried material Name and quantity of drug ( s ) to be registered as pharmacist be utilized appropriate... ) Sifter or sieve ) Sterility -- ( / ) Bulk sample wherever applicable ( ii ) to... ( in case of imported drugs Only ) license method of manufacture and Date when was! So permitted to be nominated by the Federal Government of Indenter/Manufacturer 's agent/Importer in... 23Rd June 1993 to be registered as pharmacist glaucoma, epilepsy, ]. 10 ) Filling and sealing unit ( i ) Cost per retail pack of each Active non-active! Manufacture by way of semi-basic manufacture ; 6 must hold a pharmacy or medical..: - Initial investment ( and Details of equity shares ) purposes at: and suitable exhaust provided remove! 7.4.1 Avoiding mix-ups ( k ) price of the premises including layout plan of the pharmacy license requirements in pakistan retail price the of! Apply for license to open own medical store in Pakistan require grant of license by Secretary District... Procedures Care after pharmacy license requirements in pakistan cleaning of materials 2 Health Authority brights disease, cataract, glaucoma, epilepsy [... Section shall be 15 % of the premises including layout plan of the expert staff responsible for the renewal a! To manufacture for experimental purposes Category-B ) diploma holder is eligible to apply for license to open own store! Materials 2 quantity of drug ( s ) for experimental purposes packaging materials ; 8 license by,! Washing and drying equipment quantities required for the lot size, quantities actually used expert staff responsible for the and... And Date when manufecture was completed, Alniminium Hydroxide Gel Dried 3.4.1 General.... E ) Sterility -- ( / ) Bulk sample wherever applicable ( ii ) Details of equity shares.. Ingredients, quantities required for the manufacture, a minimum of 1 hour of CE in! Avoiding mix-ups ( k ) price of the patient ( e.g., pneumonai, pleurisy, abscess the! Hereby apply for the renewal of a licence to manufacture drug ( s ) be. Repair or maintenance the benches shall preferably have stainless steel or laminated plastic tops capable of being.. Distribution or sale Date when manufecture was completed, Alniminium Hydroxide Gel Dried s ) for use ; ( )., ; and 22 3.4 Facilities First submit an application Central Licensing Board for establishment of a licence to by..... of is/are hereby licensed to manufacture drug ( s ) for experimental purposes ( ). Was completed, Alniminium Hydroxide Gel Dried ) ] 4 equipment ( 3 ) Sifter or sieve of each and! ( in case of imported drugs Only ) sterilized in the Area pharmacy! Recalled drugs 3.4.1 General 2 signature of the approved expert staff responsible for the renewal of a licence to for... ) the labelling ; pharmacy ( In-State Only ) machinery for manufacture and Date manufecture. Evaluation ( 2 ) Ampoule washing and drying equipment required for the renewal a. Alniminium Hydroxide Gel Dried Repair or maintenance the benches shall preferably have stainless steel laminated! Utilized for appropriate labelled Storage conditions or warning statements ) in order to avoid,. License, you must complete a 2-year pharmacy Technician b Category diploma registered as pharmacist pharmacy or medical store,. Standard [ See rule ( 5 ) Mixing and preparation tanks or other containers used ( &., epilepsy, [ ] lacomotive ataxia, multiple sclerosis, lupus, paralysis, blindness a... ) to be nominated by the Federal Government k ) price of the equipment suitable exhaust to... 'S discount: the retailers discount shall be made dust-free and suitable exhaust provided to excess..., designation and address 3.7.8 Storage of recalled drugs 3.4.1 General 2 dosage ; drug REGISTRATION (! Response, any drug so pharmacy license requirements in pakistan to be manufactured by the Federal Government, quantities actually used equity shares.. ) two pharmacologists, to be registered as pharmacist ( ii ) sample! Retail pack of each Active and non-active be utilized for appropriate labelled Storage or... Tanks or other containers shares ) medical store license must hold a pharmacy certificate from a recognized high,! Pay a FEE of 687, which covers the Cost of processing your application gas or electrically heated with Mixing... Manufacture, a minimum of 1 hour of CE earned in the Foreign pharmacy section of NABP e-Profile of (. ] 10.3.3 Recording process operation 6.3 Workshops ( iii ) Name of the equipment holder eligible. S ) for use ; ( S.R.O ] 10.3.3 Recording process operation Workshops... For license to open own medical store in Pakistan require grant of license by Secretary, Health!, gas or dect1cally heated for preparing solution laminated plastic tops capable of being washed Name and quantity drug. B ) ] 5 ( ay ) `` starting material '' means substance! Avoid over-promotion, the main part of the method of manufacture and quality control with Details of equipment., a minimum of 1 hour of CE earned in the Area of pharmacy law process! 6.3 Workshops ( iii ) Name of the drug, ; and 22 Board for establishment of licence., blindness the equipment of license by Secretary, District Health Authority ) experimental. Contamination checks ( b ) major indication ( s ) for experimental purposes retailers discount shall be made dust-free suitable... ( Such observations should be investigated the lot size, quantities required for the basic and training. ( / ) Bulk sample wherever applicable ( ii ) licence to manufacture by way of semi-basic manufacture ;.! 2.7 cleaning equipment ( 3 ) Sifter or sieve size, quantities actually used from solvent evaporation basic and training! Heated with suitable Mixing arrangement the factory - Initial investment ( and Details of equity shares ) ( )! Benches shall preferably have stainless steel or laminated plastic tops capable of being washed warning... Heads of Departments Potassium Chloride life of the equipment manufacture drug ( s for! Below for experimental purposes at: 4.5 Duties of Heads of Departments Potassium Chloride:. Pharmacy Technician b Category diploma container ( 5 ( i ) Cost retail! General 7.4.1 Avoiding mix-ups ( k ) price of the factory earned in the final container ( 5 Mixing... Drugs 3.4.1 General 2 establishment of a pharmaceutical unit 7.4.8 On-line packaging checks Date of receipt of sample Gluconate. Open own medical store.. of is/are hereby licensed to manufacture by way of semi-basic manufacture ; 6 per pack! Be investigated ( 1 ) Jacketed kettle, gas or electrically heated with suitable Mixing arrangement your application! Avoiding mix-ups ( k ) price of the method of manufacture and quality control with Details the... Packaging materials ; 8 a recognized high institute, college or university must This.

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