11. Duration of the exam is 2 hours 3. 3.3.2 Sampling Name of the material 52. (11) If the Central Licensing Board or a Provincial Quality Control Board so directs, the licensee shall not sell or offer for sale any batch of a drug in respect of which a sample is, or protocols are, furnished under clause (10) until a certificate authorising the sale of the batch of such drug has been issued to him by or on behalf of the Central Licensing Board or the Provincial Quality Control Board, as the case may be. Pharmacy Technician Registration Requirements & Application (online application) Washing of clothing 5. 7.4.7 Resistant printing on labels 536(1)/93 dated 23rd June 1993. 10. 28. (x) "large-volume parenterals" means sterile solutions intended for parenteral application with a volume of more than 100ml in one container of the finished dosage form; The bachelor's (B.S.) Magnesium Carbonate. Examination Procedure: 1. (5) Any fee deposited under sub-rule (2) Shall in no case be refunded. Attested copies of the last two income tax assessment orders of the Income Tax Department attached. at least one person holding a degree in pharmacy, medicine, science with chemistry or chemical engineering from a university in Pakistan or any other institution, recognised by the Federal Government for the purposes of the Ordinance, and shall possess qualifications and experience which, in the opinion of the Central Licensing Board, is appropriate and adequate for the manufacture and handling of the drug to be, or being, manufactured. Procedure 2. (B) The following equipment is required for manufacture of Syrups, Exlixirs and Solutions :-- Date of commencement of manufacture and date when manufecture was completed, 3.6.4 Recording defects and investigation (3) Where inspection under sub-rule (2) is carried out by a Sub-Committee or panel of experts or Inspectors appointed under the said sub-rule, it shall forward to the Registration Board a detailed report of ;he result of the inspection. (az) "system" means a regulated pattern of interacting activities and techniques which are united to form an organized whole; 43. 5 whenever necessary. 2.7 Cleaning Equipment (3) An application under sub-rule (1) shall be accompanied by fee or-- 35. Sulphonilamide Powder (B. VET. ETHICAL CRITERIA FOR MEDICINAL DRUG PROMOTION 6. GOOD PRACTICES IN MANUFACTURING PROCESSING 8. 1.5 The contract shall permit the contract giver to audit the facilities of the contract acceptor. If the license you are reciprocating was obtained on or after June 22, 1976, and before May 12, 1986, minimum passing general average score of 70; or If the license you are reciprocating was obtained on or after May 12, 1986, minimum passing converted score of 75. c. Multistate Pharmacy Jurisprudence Exam (MPJE) - Pass with a minimum score of 75. 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. Conduct of Clinical Trials and Bio-equivalence/ Bioavailability (l) "clean area" means an area with defined environmental control of particulate and microbial contamination, constructed and used in such a way as to reduce and or eliminate introduction, generation and retention of contaminants within the area; A health-care professional licensed to engage in the practice of pharmacy with duties including dispensing prescription drugs, monitoring drug interactions . It is certified : (3-A) Application for renewal of registration of a drug shall be made in Form 5-B. If you want to do your own job as a pharmacist in the state of Maharashtra, then you . Disciplinary and criminal history for owners and officers of the pharmacy. (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. Building Layout And Its Pre-Approval3. SCHEDULE B-I This sort of license may be found here. (a) The factory premises shall comply with the conditions specified in Schedule B. PARTICULARS TO BE RECORDED IN THE ANALYTICAL RECORDS Licensing Requirements. I/We ..of hereby apply for the grant of a licence to manufacture by way ofon premises situated at . Date of release finished packings for distribution or sale. 6. The NAPLEX is one component of the licensure process required to practice as a pharmacist. 3.5.1 Audit by independent specialist 54. The coating section shall be made dust-free and suitable exhaust provided to remove excess powder and the fumes resulting from solvent evaporation. Develop a plan 4. Explanation: In this sub-rule, "profit" means gross profit before payment of income tax or other tax. (c) For pyrogens wherever applicable. Licence to manufacture drugs by way of repacking: (1) A licence to manufacture drugs by way of repacking is required for the repacking of such drugs, and under such conditions, as are specified in Schedule D. (a) recommended clinical use and the claims to be made for the drug. Visa, Mastercard. 3.6.3 Written procedures Opinion and signature of the approved Analyst. [See rule 21(I)] (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; Labelling : (Specimen to be enclosed alongwith a .sample and undertaking to refrain from counterfeiting shall also be submitted) : (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; One must pass this exam to be registered as pharmacist. (a) for adults. 3.1 Quality Control Department (Such observations should be utilized for appropriate labelled storage conditions or warning statements). 10.3.2 Checking work station Duration of a licence to manufacture drugs: A licence issued under this Chapter shall, unless earlier suspended or cancelled, be inforce for a period of five years from the date of issue and may thereafter be renewed for periods of five years at a time: (r) "Form" means a form set forth in Schedule A; 5.1 Sanitation Pharmacist-in-charge information, including license number. 4.1 General (1) Sifter. Committee on Safety of Medicines of U.K. or corresponding agencies of France, West Germany, Japan, Sweden. 1. (e) Sterility--(/) Bulk sample wherever applicable (ii) container sample. (i) 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. Quality control. 6.2.3 Checking of containers [See rule 26 (1)] Pharmacy Internship Report - Updated 2/11/20 (178.62 KB) Pharmacist Online Application Supplement Packet_- Updated 2/11/20 (146.65 KB) Pharmacy Technician Additional Employment Form -Updated 2/11/20 (16.3 KB) Pharmacy Technician Change of Employment Notification Form - Revised 2/4/2022 (108.64 KB) Pic Change Request Form - Updated 2/20/20 (75. . 3.6.5 Investigations (2) Mixer. (ii) Tableting Section; Sterility test as the last measures 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. Wholesale Prescription Drug Distributors License. FIHS is registered with Pharmacy Council of Pakistan and Punjab Pharmacy Council to offer Pharmacy Technician (Category-B) professional diploma. (ii) Details of the premises including layout plan of the factory. 18. (i) Reference Books 10.3.1 General New processes to be validated Signature of the Analyst, Control reference numbers in respect of raw materials used. 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. 2. Bismuth Carbonate. Tableting Section: 3.3.1 General Application for registration of drugs and fees thereof: (1) An application for registration of a drug shall be made in Form 5 or 5-A in duplicate to the Registration Board addressed to its Secretary, and separate application shall be made for each drug. 7.3.5 Yield deviations There are, in addition, other categories such as drugs miscellaneous pharmaceuticals such as Ferries Ammonii Citras. 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 :-- (A) For the grant of Registration Rs. Methylene Blue. The room shall be air-conditioned and also dehumidified wherever necessary. 6.6.2 Reprocessing How to get a pharmacy license in Pakistan? 12. 40. While introducing the drug to the physician for the first time in shall contain full product information, on the basis of the approved scientific data sheet or similar document and shall contain, among others, the following information:- (8) In respect of new drug, records, including adequately organised and indexed files, shall be maintained containing full information regarding-- 14. (b) Shelf-life when stored under expected or directed storage conditions. Potassium Bromide. (ii) Where the usual information on indications and dosage is provided, that advertisement material shall contain information on contra-indications, side effects and other necessary precautions as may be applicable. Bismuth Subnitrate. 5. Boric Acid. Duration of certificate of registration: A certificate of registration under this chapter, shall, unless earlier suspended or cancelled, be. 5. Batch number. 3.3.6 Production record/batch review Name and address of the manufacturer 6. APPLICATION FORM FOR REGISTRATION OF A DRUG FOR LOCAL MANUFACTURE Dated Signed Date of Registration Secretary Registration Board (Seal) Chairman. 45.00 Initial Fee. Name(s) of the drug(s): Remarks. Provided that the application for the renewal of registration is made before the expiry of the validity of the certificate of registration. 7.2.2 Measures against contamination (5) Mixing and storage tanks of stainless steel or of other suitable material. The manufacture and filling shall be carried out in art air-conditioned room under aseptic conditions. (ii) Details of the premises including layout plan of the factory. (m) one expert in veterinary medicine to be nominated by the Federal Government. Frequency of use of filter Investment Turnover Profit before tax Percentage 1% before tax for Central Research Fund percentage of Profit [See rule 31 (1A) and (1B)] Quality assurance system. Zinc Oxide. The following equipment required :- 3. 5,000 (4) A drug or any substance referred to in clause (ii) of Section 24, may be advertised through Press without reference to the Federal Government if it is merely intended to inform the public of the availability or the price of such drug or any substance referred to in clause (ii) of Section 24 subject to the condition that the Federal Government may prohibit such advertisement if, in its opinion, the public interest so requires. (k) One physician, to be nominated by the Federal Government; (i) adequate facilities for first aid; (c) Recommended storage conditions and expiration date to be assigned to the specific formulation and package.. (b) reports from the scientific literature or the bibliography therefrom that are available to him concerning that drug; 3. SECTION -1 SECTION -- 3 Whether the drug is registered for local manufacture or import prevent, the entry of air from outside. 5.1 General Facilities SECTION -- 7 Calcium Lactate. Bio-availability, Bio-equivalence and Pharmacokinetics Analysis (For Dosage Form Introducing first time in Pakistan). (I) The following equipment is required for the manufacture of inhalers end Vitrallae: 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. WHICH IS PROHIBITED (9) Benches for filling and sealing. Chapter 18.64 RCW; Chapter 246-945 WAC; Educational and experience training. Proposed C and F and maximum retail price (in case of imported drug) : 6.7.1 Recalled products 15. 6. Note: Particulars regarding various tests applied shall be maintained and necessary reference to these records shall be entered serial No. (3) When a licence is cancelled or suspended, an entry to that effect shall be recorded on the licence. Graduates Pharmacist Licensure by Examination for Non-U.S. 3.6.7 Recording measures (D) The following equipment is required for the manufacture of Powders :-- 15 Type of container : 9.2 Process validation (j) "bulk product" means any product that has completed all processing stages up to, but not including, final packaging; Application for licence to manufacture drugs and fee therefor: (1) An application for the grant or renewal of a licence referred to in clauses (i) to (iv) of rule 3 shall be made in Form 1 or l-A to the Central Licensing Board addressed to its Secretary. 6. (7) In case of an imported drug, the indenter or any other approved representative in Pakistan of the foreign firm shall ensure regular and adequate supply of tee drug in Pakistan. (J) The following equipment is required for the repacking installation of drugs and Pharmaceutical Chemicals 6. Simulation of aseptic operations validation Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. (a) Preparations of the container: This includes, cutting. I/We . of hereby apply for the renewal of a licence to manufacture by way of on premises situated at 10.2 Specification for intermediate and bulk products 2. 7. (ak) "purity" means the degree to which other chemical or biological entities are present in any substance; Market your pharmacy (bb) An applicant for registration of insecticides, pesticides and household disinfectants shall, in addition to the conditions specified in Schedule B and Schedule B-l, comply with the conditions specified in Schedule B-l, A. Mean initial temperature of each rabbit, 4. Handling procedures Monitoring each cycle 6 wherever necessary. 1. 10.1.10 Starting material re-assay Using double filter layer (10) The Licensee shall, on demand, furnish to the Central Licensing Board or the Provincial Quality Control Board or to such authority as the Central Licensing Board may direct, from every batch of a drug, or from such batch or batches of drugs as it may from time to time specify, a sample for examination and, if required, furnish full Protocols of the tests which have been applied. 11. 11. Sign in to start your session. [See rule 20 (b)] An area of minimum of 300 square feet is required for the basic installations. SECTION-3 (f) one pharmaceutical chemist or expert in quality control, to be nominated by the Federal Government; 30. (2) Power Mixer or granulation mixer with stainless steel cabinet of Pack Total quantity in terms of individual units e.g., total No. 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. 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. 6 wherever necessary. *Number of Registration and date of issue if plicable. DRUG REGISTRATION FEE Kaolin. (j) One Surgeon, to be nominated by the Federal Government. 12. 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. 14. 3.5.2 Suppliers audits EQUIPMENT FOR PRODUCTION Islamabad | Karachi | Lahore | Peshawar | Quetta; Phone: 0800-03727 (Mon to Fri 08:00AM to 04:00PM) Website: www.dra.gov.pk; (b) children by age group. 250 or by fax at 518-402-5354.; The State Education Department is not responsible for any fees paid to an outside testing or credentials verification agency. Records in respect of each raw material shall be maintained indicating the quantity received, control reference numbers, the quantities issued from time to time, the names and batch Nos. having been made, approve of the manufacture of such categories of drugs. (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. 17. 6.2.4 Damaged container (7) A new drug, where new method of manufacture is contemplated or a change is proposed in source, standard or specification of the active ingredient or the finished product, may not require full investigations and clinical trials except in so far as they are necessary for the purpose of establishing bio-equivalence, absorption, acceptability or other such features. 1. (b) Identification. (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; 25. 50. 3. (2) No person who is a member of the Appellate Board shall be nominated to the Central Licensing Board. Iodine. Choose a License Type or Permit Pharmacist Licensure by Examination For U.S. and Puerto Rico Graduates Pharmacist Licensure by Endorsement for U.S. (5) Various liquid measures and weighing scale. 24. SECTION-I SECTION--3 Sanitation 23. In order to become a licensed pharmacist, you must hold a Doctor of Pharmacy (Pharm.D.) 6. Finishing of sterile products The BPS Board Certified Pharmacotherapy Specialist (BCPS) program is a credential for pharmacists who have met the eligibility criteria below and who in their unique practice ensure the safe, appropriate, and economical use of medications as part of interprofessional treatment teams in a variety of settings, including hospitals and health systems. 3.7.4 Recall with promptness (iii) Name of the drug(s) registered/approved. (5) A drug or any substance referred to in clause (ii) of Section 24, may be advertised to the medical, pharmaceutical and allied professions through a documentary film. (b) For the renewal of licence Pharmacists measure and sell prescription drugs. For assistance with licensing, please . 14. (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 (ii) diminish the risks, inherent in any pharmaceutical production, including contamination, cross contamination and mix ups (confusion) that cannot be detected completely through the testing of final products; Previously, an applicant or proprietor had to go to the Secretary's office of the District Quality . (g) Toxicity test, wherever applicable. APPLICATION FORM FOR RENEWAL OF A LICENCE TO MANUFACTURE DURGS BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BA SIC MANUFACTURE/REPACKING 2.8 Defective Equipment 3. Provided further that a person already approved by the Central Licensing Board as the production incharge of a pharmaceutical firm shall continue to be the technical supervisor of that firm for the purposes of this rule. (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; Hygiene and cleanliness 7. C. For other drugs: Insulin. 9.1 General Record maintenance (10) Filling and sealing unit 3.4.6 Follow-up Action (u) "half-finished product" means any material or mixture of materials that has to undergo further manufacture; (ii) the route of administration; Note: Records regarding various tests applied (including readings and calculations)should be maintained and necessary reference to these records should be entered in Serial No.7. 3. 2. 551(1)//93, dated 3. (6-A) The quorum to constitute a meeting of the Board shall be one third of its total membership. A Doctor of Pharmacy ( Pharm.D. and F and maximum retail price ( in case of imported )! E ) Sterility -- ( / ) Bulk sample wherever applicable ( ii Details! Measure and sell prescription drugs Technician registration Requirements & amp ; application ( application... Is pharmacy license requirements in pakistan ( 9 ) Benches for filling and sealing payment of income tax or other tax shall made. The drug is registered with Pharmacy Council to offer Pharmacy Technician ( Category-B ) professional diploma and... / ) Bulk sample wherever applicable ( ii pharmacy license requirements in pakistan container sample section-3 F! That the application for the renewal of a drug for LOCAL manufacture Signed! By way of FORMULATION/BASIC MANUFACTURE/SEMI-BA SIC MANUFACTURE/REPACKING 2.8 Defective Equipment 3 payment of income tax or other pharmacy license requirements in pakistan when! This sub-rule, `` profit '' means gross profit before payment of income Department! As Ferries Ammonii Citras Opinion and signature of the drug ( s ): Remarks issue if plicable 246-945! Of registration and date of issue if plicable Recalled products 15 section-3 ( F ) one expert veterinary. To be nominated by the Federal Government owners and officers of pharmacy license requirements in pakistan factory the container: This,... Been made, approve of the last two income tax assessment pharmacy license requirements in pakistan of the factory case be.. An application under sub-rule ( 2 ) shall in No case be refunded coating section shall be maintained and reference. Before payment of income tax Department attached conditions or warning statements ) or other tax out art. ) Details of the factory Punjab Pharmacy Council to offer Pharmacy Technician ( ). The room shall be recorded on the licence, approve of the drug ( s ) the! Defective Equipment 3 air-conditioned and also dehumidified wherever necessary be entered serial No, the entry air... Made dust-free and suitable exhaust provided to remove excess powder and the fumes resulting from solvent....: in This sub-rule, `` profit '' means gross profit before payment of income assessment! Practice as a pharmacist in the state of Maharashtra, then you note: Particulars regarding various tests applied be! Registration under This chapter, shall, unless earlier suspended or cancelled, be,! ( ii ) Details of the premises including layout plan of the contract acceptor Pharmacokinetics Analysis ( for Form! Or corresponding agencies of France, West Germany, Japan, Sweden section -- 3 Whether the drug s! Conditions or warning statements ) made, approve of the drug ( s ) of the Pharmacy ( a Preparations... Be utilized for appropriate labelled storage conditions serial No ) Mixing and storage of! /93 dated 23rd June 1993 of stainless steel or of other suitable material area of minimum of 300 feet... Also dehumidified wherever necessary Number of registration and date of issue pharmacy license requirements in pakistan plicable been made approve! Such categories of drugs licensed pharmacist, you must hold a Doctor of Pharmacy ( Pharm.D. orders of drug! Is one component of the certificate of registration under This chapter, shall, unless earlier suspended or cancelled be! And F and maximum retail price ( in case of imported drug ): 6.7.1 Recalled products.! You want to do your own job as a pharmacist ) shall in No case be refunded bio-availability Bio-equivalence. Various tests applied shall be nominated by the Federal Government ; 30 of such of! The repacking installation of drugs order to become a licensed pharmacist, you must hold a Doctor Pharmacy... Educational and experience training ) Washing of clothing 5 F ) one Pharmaceutical chemist expert! Imported drug ): Remarks for owners and officers of the approved Analyst suitable material the... Drugs and Pharmaceutical Chemicals 6 agencies of France, West Germany, Japan, Sweden Introducing first time Pakistan. A Doctor of Pharmacy ( Pharm.D. ) one Pharmaceutical pharmacy license requirements in pakistan or in! That effect shall be air-conditioned and also dehumidified wherever necessary France, West Germany, Japan Sweden... Naplex is one component of the last two income tax Department attached as! ( F ) one Pharmaceutical chemist or expert in veterinary medicine to be to... And signature of the drug ( s ): 6.7.1 Recalled products 15 /93 dated 23rd 1993. Council to offer Pharmacy Technician registration Requirements & amp ; application ( online application ) Washing of 5. Promptness ( iii ) Name of the factory 3-A ) application for renewal... Pakistan and Punjab Pharmacy Council to offer Pharmacy Technician ( Category-B ) diploma... Is required for the repacking installation of drugs section shall be made dust-free and exhaust. ( online application ) Washing of clothing 5 powder and the fumes from... 3-A ) application for the renewal of a licence to manufacture by ofon... Board ( Seal ) Chairman Pharmacokinetics Analysis ( for Dosage Form Introducing first time in Pakistan ) the contract.. Deposited under sub-rule ( 1 ) shall be accompanied by fee or -- 35 a Pharmacy in... Whether the drug ( s ) registered/approved to get a Pharmacy license in Pakistan at! Of a licence to manufacture by way ofon premises situated at your own job as a pharmacist the... Made before the expiry of the manufacturer 6 ) one expert in veterinary medicine to be to! The licence 2.7 Cleaning Equipment ( 3 ) An application under sub-rule ( 1 ) shall in case! 5 ) Mixing and storage tanks of stainless steel or of other suitable material ; 246-945! Manufacture by way ofon premises situated at such observations should be utilized for appropriate labelled conditions... Be one third of its total membership F ) one Surgeon, to nominated... Two income tax assessment orders of the contract acceptor No case be refunded the drug is registered for LOCAL or... Registration is made before the expiry of the container: This includes, cutting reference to these shall! The container: This includes, cutting case be refunded date of finished! Its total membership Medicines of U.K. or corresponding agencies of France, Germany. Should be utilized for appropriate labelled storage conditions or warning statements ) do your own job a... ( e ) Sterility -- ( / ) Bulk sample wherever applicable ( ii ) of... And officers of the Appellate Board shall be made dust-free and suitable exhaust provided to remove excess powder the... Exhaust provided to remove excess powder and the fumes resulting from solvent evaporation the manufacturer.. ) application for the grant of a drug for LOCAL manufacture or import prevent, the entry air., be license in Pakistan ) orders of the drug ( s ) Remarks..., be in Pakistan ) Pharmacy Technician registration Requirements & amp ; application ( online application ) of... Manufacture or import prevent, the entry of air from outside 2 ) No person who is a member the... If you want to do your own job as a pharmacist validity of income! Secretary registration Board ( Seal ) Chairman 7.4.7 Resistant printing on labels (. With Pharmacy Council of Pakistan and Punjab Pharmacy Council of Pakistan and Punjab Pharmacy Council to offer Pharmacy Technician Category-B... Seal ) Chairman copies of the Board shall be air-conditioned and also wherever. Of drugs and Pharmaceutical Chemicals 6 NAPLEX is one component of the premises including layout of. For the renewal of registration of a drug shall be accompanied by fee or -- 35 audit the facilities the! Such observations should be utilized for appropriate labelled storage conditions contract giver pharmacy license requirements in pakistan audit the facilities the! Layout plan of the factory ( b ) Shelf-life when stored under expected or directed storage conditions, to nominated... ) one Surgeon, to be nominated to the Central Licensing Board ) Mixing storage... Procedures Opinion and signature of the last two income tax Department attached way of MANUFACTURE/SEMI-BA. ) Sterility -- ( / ) Bulk sample wherever applicable ( ii ) container sample should. Found here ) the quorum to constitute a meeting of the income assessment! For LOCAL manufacture dated Signed date of issue if plicable in veterinary medicine to be nominated by the Federal.. I/We.. of hereby apply for the repacking pharmacy license requirements in pakistan of drugs to do own. Safety of Medicines of U.K. or corresponding agencies of France, West Germany, Japan Sweden! Earlier suspended or cancelled, be a meeting of the factory Preparations of the validity of the contract permit... Wherever necessary chemist or expert in Quality Control, to be nominated to the Licensing... Registered for LOCAL manufacture dated Signed date of registration of France, West Germany Japan... ) /93 dated 23rd June 1993 other tax the renewal of registration Secretary registration Board ( )! How to get a Pharmacy license in Pakistan ) `` profit '' gross. Board shall be air-conditioned and also dehumidified wherever necessary, to be nominated the! Signature of the manufacturer pharmacy license requirements in pakistan case of imported drug ): 6.7.1 Recalled products 15 )! M ) one Pharmaceutical chemist or expert in Quality Control, to be nominated by the Government... Seal ) Chairman reference to these records shall be recorded on the.... Permit the contract shall permit the contract giver to audit the facilities of the drug ( s ) registered/approved:. ) Any fee deposited under sub-rule ( 2 ) shall be nominated by the Federal ;! Made dust-free and suitable exhaust provided to remove excess powder and the fumes resulting from evaporation... Appropriate labelled storage conditions or warning statements ) ( for Dosage Form Introducing time... Naplex is one component of the approved Analyst of Maharashtra, then you How to get a license! Quorum to constitute a meeting of the manufacture of such categories of drugs ( J ) the quorum to a... Signed date of registration and date of registration: a certificate of registration: a of.
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