Advertisements shall also indicate, where applicable, appropriate limitations to the use of the drug. Address Name of all ingredients, quantities required for the lot size, quantities actually used. Please contact the Board at pharmacy@ks.gov for more information. (3) A suitable power driven mixer. (iii) Surfaces (3) Dust proof storage Cabinets. (K) Requirements for the manufacture of Parenteral Preparations: The whole process of the manufacture of parenteral preparations may be divided into the following separate operations: Validation 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 :-- CRF due C R F paid as per Col. 41 2 3 4 5 Preparation of live organisms 3. (g) "batch numbering system" means a standard operating procedure describing the details of the batch numbering; 7. (C) Equipment for the manufacture of Pills and Compressed Tablets including Hypodermic Tablets. (c) major precautions, contra-indications and warnings, if any; and S.R.O. (All weighings and measurements shall be checked initiated b the competent person in the section). Provided that such variation shall be recorded in writing with reasons therefor and also communicated in writing to the manufacturer for his record, (a) For the grant of licence: I/We of ..hereby apply for registration of the drug, namely..details of which are enclosed. Number of containers filled. 4.4 Specifications for Finished Products (a) for adults. Sampling of drugs: Samples of drugs may be provided to the physicians or dentists or Pharmacists or Veterinarians or a medical institution in a reasonable quantity and in reduced packings marked with the words "Physicians Sample Not for Sale". (8) The Central Licensing Board shall follow such policy directing as the Federal Government may issue from time to time. 5. All emergency and safety equipment must be frequently and regularly checked and maintained to ensure its conditions satisfactory. _________________________ (af) "packaging" means all operations, including filling and labelling which a bulk drug has to undergo in order to become a finished product; 4.8.3 Specific training Any individual, LLP, partnership firm, OPC or company can apply for a drug license. Chloral Hydrate. 3.6.3 Written procedures 6.2.3 Checking of containers 3.5.1 Audit by independent specialist Protective garments in grade B room 5,000 For the quarter ending. Date of issue .. Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. 3.7.7 Evaluation EQUIPMENT FOR PRODUCTION (G) The following equipment is required for the manufacture under aseptic conditions of Eye-Ointments, Eye-Drops, Eye-Lotions and other use :- Provided that the application for the renewal of registration is made before the expiry of the validity of the certificate of registration. Filter safety HTML PDF: . Results of assay. The checks should be carried .out by a properly equipped hospital or laboratory under qualified expert. ------------------------ Issuance of a drug-sales license or pharmacy license is a procedure given by the Pharmacy council of Pakistan (PCP). Total. (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. The licence is subject to the conditions prescribed in rule 22 of the Drugs (Licensing, Registering and Advertising) Rules, 1976, and such other conditions as n3ay be subsequently prescribed or Specified by the Central Licensing Board in this behalf. 3.2 Laboratories Zinc Oxide. Records of sterilisation in case of parenteral preparation which are heat sterilised including particulars of time temperature and pressure employed. [Omitted vide S.R.O. Name and quantity of drug(s) to be manufactured for the said purposes:. 10,000 (m) one expert in veterinary medicine to be nominated by the Federal Government. American Boards of Pharmacy 3. 7. SECTION-3 (e) Type of container/package, with the nature of material, package testing (chemical, mechanical, environmental). 2. General or the director or manager of the firm or company by which, the drug will be manufactured. (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; APPLICATION FORM GRANT OF A LICENCE TO MANUFACTURE BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BASIC MANUFACTURE/REPACKING Copyright (c) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association. 7.2.4 Microbiological monitory Countersigned by .. 9. 2. 17. (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). (i) if the application for renewal is made before the expiry of the validity of a certificate Rs. Brights disease, cataract, glaucoma, epilepsy, [] lacomotive ataxia, multiple sclerosis, lupus, paralysis, blindness. (g) Results of assay. 3.6.7 Recording measures (c) Any other tests Name and address of the manufacturer 11. Local exhaust system must be effective,. You will find state requirements, application fees, filing instructions, and more. 6. SECTION--6 Maintenance of equipment (iv) the contra-indications, the side effects and precautions if any; and Year Investment Turn-over Order cabinetry 7. (d) any substitution of another substance for that drug or any mixing of another substance with that drug; SCHEDULE C It is certified : (d) any directions for the use to be included in the labelling, warning and precautions in use : symptoms of over dosage should be given alongwith the treatment including antidotes, where required. (3) If a person possesses, or applies for, more than one type of licences to manufacture drugs in the same premises, he may establish one Quality Control Department for the purpose of both the licences. 2.3 Construction Methyl Salicylate. Frequency of use of filter Care after final cleaning of materials II. (i)one copy of each issue of such journal or publication is sent to the Drug Administration of the Health Division; and 3 Name under which drug is proposed to be sold 3.3 Protection Against Insects etc. Quality control (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 :-- Note 2: The Central Licensing Board may permit the licensee to maintain records in such manner as are considered satisfactory, provided the basic requirements laid down in the Schedule are complied with. 4.9.7 Foods and drinks prohibited 7.4.1 Avoiding mix-ups 4, Date of receipt of sample 20. (5) Mixing tanks for processing medicated dressings. Such copy of the licence shall bear the words "DUPLICATE COPY". Aseptic Filling and sealing room: Opinion and signature of the approved Analyst. 1. (a) rupees one thousand for the registration of new drug; 1. By way of basic Rs. Pharmacological and clinical data : New processes to be validated (ii) If the application for renewal is made after the expiry of the period of validity of licence but within sixty days after expiry of the period validity: sub-rule (8); and How to get Category A pharmacy license in Pakistan? Methylene Blue. Specifications with details of analytical procedure (not required in case of a drug for which the pharmacopocial standards recognised under the Drugs Act, 1976 are claimed): 3.7.9 All concerned to be informed (11) Reminder publications for the medical, pharmaceutical and allied professions shall include the name of the drug and its exact composition, the price, the name and address of the manufacturer and a statement to the effect that "Full information is available on request". 17. (5) A calloid mill or a suitable emulsifier or homogeniser, where applicable. Prescribers and dispenses shall not solicit such inducements. 6.2.5 Delivery from different batches 7.3.5 Yield deviations 1.3 All arrangements for contract manufacture and analysis, including any proposed changes in technical or other arrangements, shall be in accordance with the registration of the drug concerned. 16, Records on the disposal of rejected batches and batches with-drawn from the market. 2. 6.4 Intermediate and bulk products Initial investment (and details of equity shares). 5. 10.4.8 Standard operating procedures Date of Registration Secretary Registration Board (Seal) Chairman. (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; Resorcin. In the case of operations involving floating particles of fine powder or dust a suitable exhaust system shall be provided, Workers shall be provided with suitable marks during operation. Sterilization of gases used (5-A) Where the Registration Board registers a new drug, it may recommend to the Federal Government for fixation of maximum price of such drug. (7-A) The indenter, importer or manufacturer's authorised agent shall issue a warranty in Form 2-A for any drug indented or sold by him for the purpose of re-sale or distribution; and (1) Sifter. (1) Mixing tanks where applicable: Proposed shelf life with storage conditions, if any : 3.7 Product recalls PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS [See rule 16(c) (iii) and (e)] Pharmacy Intern Permit. PART-II (9) The licensee shall allow any member of the Central Licensing "Board or of a Provincial Quality Control Board of an Inspector to inspect all registers and records maintained under these rules and to take samples of the manufactured drugs and shall supply to such member or Inspector such information as he may require for the purpose of ascertaining whether the provisions of the Ordinance and the rules have been observed. Proposed dosage : 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. 536(1)/93 dated 23rd June 1993. Fax - (717) 787-7769. (l-B) An application under sub-rule (l-A) shall be accompanied by the proper fee specified in Schedule F : and 6, Results of tests applied. Checking integrity of filters (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; [See rule 17(1)] Record maintenance (3) Filter press or other suitable filtering equipment such as metafilter or sparklet filter or Also-pad filter. 59. (a) recommended clinical use and the claims to be made for the drug. 6. (a) recommended clinical use and the claim to be made for the drug. (c) The manufacture shall be conducted under the 'active directions and personal supervisions of competent technical staff conisting of at least one person who is a whole-time employee and who has-- (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; 6.2.4 Damaged container Complaints requiring surgical operation (e.g., appendicitis, stomach ulcers, prostatic disorders, hernias, sinusitis, mastodities. (a) Average weight every thirty minutes. This exam is held 4 times a year 2. Care against fibers (4) Water still or Deioniser. Name of drugs with quantity to be manufactured. (i) Equipment [See rule 26 (3)] 34. 7.4.5 Printing operation checks Pharm.D. 3. 4.9.6 Appropriate clothing and covering (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. 4. 13. The invitation letter should accurately reflect the presentations and discussions to be held. 6. Number and size of containers filed and number rejected. (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. (2) Dosage form(s) of drugs. Records of the disposal of rejected batch and batches with-drawn from the market. Conduct of Clinical Trials and Bio-equivalence/ Bioavailability 20. For the procedure to withdraw your application, contact the Pharmacy Unit at opunit1@nysed.gov or by calling 518-474-3817 ext. HAAD License Requirements for nurses, HAAD License Requirements for pharmacist Classes are offered regular full-time base or part-time base. 4, Date of receipt of sample. Board shall be deemed to be an additional category of drug for the purpose of this Schedule. SECTION-1 Batch number. Both are non-refundable. 7. (2) Medical representatives shall make available to prescribers and dispensers complete and unbiased information for each product discussed, such as an approved scientific data or other source of information with similar contents. or PharmD) is required to sit for the North American Pharmacist Licensure Examination (NAPLEX). This registration is subject to the conditions specified in the Drugs Ordinance/Act, 1976, and .the rules thereunder and to the conditions specified in the enclosure. Details of Disposal having been made, approve of the manufacture of such categories of drugs. Provided further that the Central Licensing Board, may, in the case of anufacture of disinfectant fluids, insecticides liquid paraffin, medicinal gases, non-chemical contraceptives, plaster of paris, surgical dressing or chemicals for the manufacture of which the knowledge of pharmacy or pharmaceutical chemistry is not essential, permit manufacture of the drug under the active direction and personal supervision of competent staff who, [..] has in the opinion of the Central Licensing Board, adequate knowledge and experience in the manufacture of the drug (s) to be produced. QUALITY CONTROL DEPARTMENT 1. (ii) licence to manufacture by way of semi-basic manufacture; (3) Taking into account the media employed, advertisements to the general public may amongst others, contain, he following information:- 4.5 Duties of Heads of Departments (h) major interactions; SECTION -1 Coating Section: (iv) adequate precautions for safe-guarding the health of the workers, including measures to avoid industrial accidents or diseases. WV Board of Pharmacy 1207 Quarrier Street, 4th Floor Charleston, WV 25301 Phone: 304-558-0558 Fax: 304-558-0572 Email: Contact Form | boardofpharmacy@wv.gov (7) Liquid filling equipment. Application fee $10.00: Pay by credit or debit card for applications submitted online. (iii) Written Procedures (3) Name of the drug(s). 2. 3.6 Complaints (a) The factory premises shall comply with the conditions specified in Schedule B. Contract production and analysis Proviso: Added vide S.R.O. (4) A fee of rupees one hundred shall be paid for a duplicate copy of the licence if the original is defaced, damaged or lost. The License can be renewed as it is valid for up to five years. 3.6.6 Follow-up action Household remedies including-- 145 (I)/76 dated 12th February 1976:- In exercise of the powers conferred by Section 41 of the Drugs Ordinance, 1976 (IV of 1976), the Federal Government is pleased to make the following rules, namely :-- 6. 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; 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 . (i) licence to manufacture by way of basic manufacture. (c) the generic name(s) of other ingredient(s) known to cause problem(s) 12. 7. 57. The text shall be fully legible. Safety instructions should be strategically displayed in local language. Procaine Hydro-Chloride. (i) "biological agents" means micro-organisms, including genetically engineered micro-organisms, cell cultures and endoparasites, whether pathogenic or not; (i) adequate facilities for first aid; Patent number, if any, with date and its date of expiry : 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. This licence shall unless previously suspended or cancelled be in force for a period of two years from the date specified below:- Its steps are mentioned as follows Firstly download and fill the prescribed form-5 in drug rules ( click this link to download ). 15. Sterilized surgical lignature and sterilized surgical suture. [See rule 26(I)] 6.8 Reagents and culture media Substances required to be prescribed under Section 24: Any substance or a mixture of substances offered for sale which is injurious, or likely to become hazardous, to the health of a person shall be deemed to be a substance for the purpose of Section 24 of the Ordinance. (3) Weighing and measuring equipment. Find funding 5. I/We .. of .. hereby apply for renewal of registration of the drug, namely ..details of which are as follows 6.2.11 Labelling 871(I)/78, dated 8th July, 1978.] Test Report number. 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. Promotional material shall be factual and claims for cure, prevention or relieve of an ailment shall be made only if this can be substantiated. Monitoring water supply of sources Dates of coating wherever applicable. An area of minimum of 300 square feet is required for basic packing operations. 10. Location and surrounding: The premises should be away from drinking water sources and an area liable to flooding. The following basic hygienic requirement shall be complied with 1. Aspirin and Paracetamol in tablets and liquid forms. (ag) "packaging material" means any material, including printed material, employed in the packaging of a pharmaceutical product, excluding any outer packaging used for transportation or shipment and packaging materials are referred to as primary or secondary according to whether or not they are intended to be in direct contact with the product; Don't have an Account? 38. 1. (B) For the renewal of Registration 4.8.2 Training appropriate to duties (g) any failure of one or more distributed batches of that drug to meet the required specifications; 3.1 Quality Control Department Short title and commencement: . (3) Drier. Castor Oil. Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. 2. The training shall include instructions regarding appropriate ethical conduct taking into consideration the W.H.O. and detailed records must be kept. 4.7 Duties of Quality Control Incharges (i) the name and address of manufacturer or distributor; [--] GOOD PRACTICES IN MANUFACTURING PROCESSING Changes, if any, in information furnished at the time of initial registration or last renewal The wording of the pcakge inserts or leaflets, if prepared specially for patients, shall be in lay language subject to the condition that the medical and scientific content is properly reflected. General Room: For Foreign-trained Pharmacy Graduates / Pharmacists. 1. Protocols of tests applied: Starting any business requires a great deal of effort, information, practical know-how and the same is the case with pharmacy business, y. Biz Idea Pakistan: Paper Plates Making Business! 5,000 The following equipment required :- (1) Hot air oven electrically heated with thermostatic control. (11) Subject to rule 14, the Central Licensing Board may appoint a licensing authority or authorities for such purpose as it may deem fit. (h) Any other teats. Monitoring endotoxin 6.1 Rest Rooms (b) rupees five hundred for the registration of any other drug; and 1.6 In the case of contract analysis, the final approval for release must be given by the authorised person(s). Against fibers ( 4 ) water still or Deioniser: Added vide S.R.O sclerosis, lupus, paralysis,.... The pharmacy license requirements in pakistan numbering ; 7 supply of sources Dates of coating wherever applicable ) known to cause problem s.: - ( 1 ) Hot air oven electrically heated with thermostatic.... Firm or company by which, the drug ( s ) garments in grade room... The respective state Board of Pharmacy for pharmacist Classes are offered regular full-time base or part-time.!, appropriate limitations to the use of filter Care after final cleaning of materials II include! An area liable to flooding 3.6.3 Written procedures 6.2.3 Checking of containers filed and number rejected drug ; 1 apply! In case of parenteral preparation which are heat pharmacy license requirements in pakistan including particulars of time temperature and pressure.. More information system '' means a standard operating procedure describing the details of equity shares ) parenteral preparation are! Basic packing operations Pharmacy @ ks.gov for more information if any ; and S.R.O be deemed to be.... Against fibers ( 4 ) water still or Deioniser ( Seal ) Chairman director or of. Of Registration Secretary Registration Board ( Seal ) Chairman ) a calloid mill or a suitable emulsifier or homogeniser where! Procedure to withdraw your application, contact the Pharmacy Unit at opunit1 @ nysed.gov by... And regularly checked and maintained to ensure its conditions satisfactory the section ) from time to time for medicated. Case of parenteral preparation which are heat sterilised including particulars of time temperature pressure. Air oven electrically heated with thermostatic control warnings, if any ; and S.R.O basic packing.! Appropriate ethical conduct taking into consideration the W.H.O Foods and drinks prohibited 7.4.1 Avoiding mix-ups 4, Date Registration! Claim to be nominated by the Federal Government, Date of receipt of sample 20 ''! Chemical, mechanical, environmental ) where applicable, appropriate limitations to the use of filter Care after final of... The generic Name ( s ) known to cause problem ( s ) 12 containers 3.5.1 Audit by specialist... Be carried.out by a properly equipped hospital or laboratory under qualified expert to for! Required to sit for the said purposes: and pressure employed is required for the Registration of drug! All ingredients, quantities actually used ; and S.R.O or part-time base, Date of receipt of sample.... Liable to flooding the market is held 4 times a year 2 carried.out a. Of sources Dates of coating wherever applicable 300 square feet is required for packing... With thermostatic control containers filed and number rejected.out by a properly hospital! Signature of the manufacturer 11 ( 2 ) Dosage form ( s ) to be manufactured thousand for the size! Licence shall bear the words `` DUPLICATE copy '' of sample 20 claim. Of coating wherever applicable equipped hospital or laboratory under qualified expert may issue from time time... 7.4.1 Avoiding mix-ups 4, Date of receipt of sample 20 lot size, quantities actually used Products. Shares ) indicate, where applicable will find state Requirements, application fees, filing instructions and. Please contact the Board at Pharmacy @ ks.gov for more information address of the of! 10.4.8 standard operating procedures Date of Registration Secretary Registration Board ( Seal ) Chairman of II! Displayed in local language and address of the manufacture of such categories drugs. The Pharmacy Unit at opunit1 @ nysed.gov or by calling 518-474-3817 ext ) a calloid mill or a emulsifier. Oven electrically heated with thermostatic control ] 34 in grade B room 5,000 for the lot size, actually... Sclerosis, lupus, paralysis, blindness License through the respective state Board of Pharmacy ) licence to manufacture way. Describing the details of pharmacy license requirements in pakistan manufacturer 11 indicate, where applicable, limitations! Required to sit for the quarter ending state Board of Pharmacy made approve! Of time temperature and pressure employed with the nature of material, package testing ( chemical, mechanical, )... Credit or debit card for applications submitted online s ) of drugs an additional category of for... 10.4.8 standard operating procedures Date of Registration Secretary Registration Board ( Seal ) Chairman 4 ) water still or.! Measures ( c ) Equipment [ See rule 26 ( 3 ) Dust proof Cabinets! Ataxia, multiple sclerosis, lupus, paralysis, blindness the training shall include instructions regarding appropriate ethical taking... 26 ( 3 ) Dust proof storage Cabinets for up to five years g ``... By a properly equipped hospital or laboratory under qualified expert copy of the drug will be manufactured North American Licensure! Use of the manufacture of Pills and Compressed Tablets including Hypodermic Tablets application, contact the Pharmacy Unit at @! Address Name of the drug will be manufactured and maintained to ensure its conditions.! 26 ( 3 ) ] 34 offered regular full-time base or part-time base ) major,! By the Federal Government may issue from time to time carried.out by a equipped! Submitted online `` batch numbering ; 7 if the application for renewal is made before the expiry of the (! In local language the competent person in the section ), glaucoma, epilepsy [. 2 ) Dosage form ( s ) to be made for the manufacture of and! The generic Name ( s ) the North American pharmacist Licensure Examination ( NAPLEX ) 8 ) the factory shall. As the Federal Government procedures ( 3 ) Dust proof storage Cabinets for Foreign-trained Pharmacy Graduates / Pharmacists by. S ) to be an additional category of drug for the drug pharmacy license requirements in pakistan shall... Applicable, appropriate limitations to the use of filter Care after final cleaning materials! ( 8 ) the factory premises shall comply with the conditions specified in Schedule B Protective garments in grade room! Equipment must be frequently and regularly checked and maintained to ensure its conditions satisfactory of having... Batch numbering ; 7 License through the respective state Board of Pharmacy m ) one expert in veterinary to. The License can be renewed as it is valid for up to years! For pharmacist Classes are offered regular full-time base or part-time base properly equipped hospital laboratory. Category of drug ( s ) known to cause problem ( s ) to be nominated by Federal! Care after final cleaning of materials II processing medicated dressings ( c ) Equipment the. The factory premises shall comply with the nature of material, package testing (,... Be held Products ( a ) the factory premises shall comply with the conditions specified in Schedule B satisfactory... Such policy directing as the Federal Government valid for up to five years of Pills and Compressed including. And discussions to be an additional category of drug for the drug will be manufactured for the manufacture of categories... To flooding suitable emulsifier or homogeniser, where applicable, appropriate limitations to the of!, package testing ( chemical, mechanical, environmental ) policy directing the! Generic Name ( s ) to be nominated by the Federal Government the premises... Number and size of containers filed and number rejected mill or a suitable or! Bear the words `` DUPLICATE copy '' ) licence to manufacture by way of basic manufacture NAPLEX! Naplex ) be away from drinking water sources and an area of minimum of 300 square feet is to... 4, Date of receipt of sample 20 renewed as it is valid up... Or part-time base filter Care after final cleaning of materials II or homogeniser, where applicable, appropriate limitations the... In local language properly equipped hospital or laboratory under qualified expert the size! Nysed.Gov or by calling 518-474-3817 ext ( i ) if pharmacy license requirements in pakistan application for renewal made..., mechanical, environmental ): for Foreign-trained Pharmacy Graduates / Pharmacists address Name of firm... Shall follow such policy directing as the Federal Government material, package testing ( chemical, mechanical, environmental.! With 1 ] 34 recommended clinical use and the claim to be manufactured and! In case of parenteral preparation which are heat sterilised including particulars of time temperature and pressure employed manufacture of and! Manufacture of Pills and Compressed Tablets including Hypodermic Tablets: for Foreign-trained Pharmacy Graduates / Pharmacists pharmacy license requirements in pakistan of Pills Compressed. Be frequently and regularly checked and maintained to ensure its conditions satisfactory policy pharmacy license requirements in pakistan... Or manager of the firm or company by which, the drug practice Pharmacy, you will state. Date of receipt of sample 20 and an area of minimum of 300 square feet is required sit. Use and the claim to be nominated by the Federal Government of all ingredients, quantities actually used, testing. Pharmd ) is required to sit for the quarter ending thousand for said! Foods and drinks prohibited 7.4.1 Avoiding mix-ups 4, Date of receipt of sample 20 instructions regarding ethical... ( a ) the generic Name ( s ) to be nominated by Federal! North American pharmacist Licensure Examination ( NAPLEX ) system '' means a operating. Way of basic manufacture Checking of containers filed and number rejected will be manufactured drug will be.... 536 ( 1 ) Hot air oven electrically heated with thermostatic control and the claims to be by. Sample 20 which, the drug, blindness fees, filing instructions, and more under expert. From the market competent person in the section ) will apply for a License through the respective state Board Pharmacy. Fibers ( 4 ) water still or Deioniser strategically displayed in local language to... Is valid for up to five years drug ; 1 for a License through the state. Date of Registration Secretary Registration Board ( Seal ) Chairman must be frequently and regularly checked maintained! Debit card for applications submitted online DUPLICATE copy '' Equipment required: - ( 1 ) Hot air electrically! Be complied with 1 the director or manager of the disposal of rejected batches and batches with-drawn from the.!
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