SCHEDULE B (4) Stainless steel vessels and scoops of suitable material, Bio-availability studies: Previously, an applicant or proprietor had to go to the Secretary's office of the District Quality . (2) Stainless steel scoops end vessels. 20. (2) Mixer. 10. Airlock system 1. 3.4 Surfaces or an officer of the Provincial Health Department not below the status of Additional Secretary, to be nominated by the Secretary, Health Department of that Province. 48. 39. Central Licensing Board: (1) The Central Licensing Board shall consist of the following members, namely :-- (c) The licensee shall either in his own laboratory or, where so authorised under the proviso to clause (e) of rule 16, in any other laboratory approved by the Central Licensing Board, test each batch of the raw materials used by him for the manufacture of drugs and also each batch of the final drug, shall maintain records showing the particulars in respect of such tests as specified in Schedule B-III and shall retain such records, in the case of a substance for which expiry date is fixed for a period of two years from the expiry of such date and, in the case of other substances, for a period of five years from the date of manufacture. (h) any unexpected side effects, injury, toxicity or sensitivity reaction associated with the clinical uses, studies, investigations and tests respecting that drug; and (u) "half-finished product" means any material or mixture of materials that has to undergo further manufacture; Sodium Bromide. SECTION--6 3.3.1 General RECORDS OF RAW MATERIALS Visa, Mastercard. Explanation: In this sub-rule, "profit" means gross profit before payment of income tax or other tax. (2) Analgesic Balms/Plasters. (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. 10. 13. Graduates Pharmacist Licensure by Endorsement for Non-U.S. Analytical report number. 11. (c) The manufacture shall be conducted under the active directions and personal supervision of competent technical staff consisting of. 16. (e) Disintegration test (time in minutes). PROFORMA 6.3.2 Printed materials Fumigation Introduction . The walls and floor shall be such as may permit their being sprayed and washed with an antiseptic solution. Ephedrine Hadrochloride. 10,000By way of semi-basic Rs. C.). (2) The import, manufacture and sale of drugs shall be in accordance with the information contained in the applications in respect of those drugs or in any supplementary information or, where such information was amended by the Registration Board, in accordance with such amended information on the basis of which such drugs were registered: By way of formulation Rs. For Foreign-trained Pharmacy Graduates / Pharmacists. An area of minimum of 200 square feet is required for the basic installations. Dated Signed ETHICAL CRITERIA FOR MEDICINAL DRUG PROMOTION 8. (g) any failure of one or more distributed batches of that drug to meet the required specifications; (5) Filling equipment, The Registration Board after getting the said intimation shall take similar action for the same drug available from other sources within the shortest possible time; Date of release of finished packings for distribution or sale, is/are hereby licensed to manufacture by way of Basic Manufacture/Semi Basic manufacture/Formulation/Repacking at the following premises:- The drug(s) or class(es) of drugs intended to be manufactured :- 5.3 General Requirements for Production Areas Contract production and analysis HTML PDF: 246-945-245: Health care entity license. (d) special groups, 10.1.1 Maintenance of documents 3. (3) Sifter or sieve. New processes to be validated Year Investment Turn-over 6.7.1 Recalled products Ammonium Bicarbonate. (f) "batch number (or lot number)" means a distinctive combination of numbers and or letters which specifically identifies a batch on the labels, the batch records, the certificates of analysis, and that permit the production history of the batch to be traced and revived. 7. 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. 11. SECTION--2 8. (b) rupees five hundred for the registration of any other drug; and 10.3.1 General Hygiene and cleanliness Researching legal requirements is an important step in learning how to open a pharmacy, and you want to ensure that you have everything properly set-up before opening your business. I enclose :- (6) The Registration Board shall, before registering a new drug for which the research work has been conducted in other countries and its efficacy, safety and quality has been established therein, require the investigation on such pharmaceutical, pharmacological and other aspects, to be conducted and clinical trials to be made as are necessary to establish its quality and, where applicable, the biological, availability, and its safety and efficacy to be established under the local conditions: Sodium Sulphate. The applicant must be a graduate with a university degree * accepted by Singapore Pharmacy Council. 6.11 Miscellaneous 4.9.4 Reporting health problems Types of licences to manufacture drugs: Licences to manufacture drugs shall be of the following types, namely :-- (iii) Name of the approved expert staff. 6.8 Reagents and culture media 4.7 Special Materials Invoice/Challan number and date. We recommend that you send all supporting documentation to NABP at the time of submitting your application. The application fee is $147. Local exhaust system must be effective,. (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; 6.6.1 Storage and disposal An area of minimum of 250 square feet is required for the basic installation. Registration Board: (1) The Registration Board shall consist of such members, including the 11. Water supply Bioburden to be minimal open lesions or skin infection shall be engaged in production areas. 2.3 The contract giver shall ensure that all processed products and materials delivered by the contract acceptor to comply with their specifications or that the product has been released by the authorised person(s). Potassium Citrate. (7) The licensee shall comply with the provisions of the Ordinance and the rules and with such further requirements, if any, as may be specified in any rule subsequently made-in this behalf or any other condition that may be imposed at the time of grant of a licence in the special circumstances of each case. Certified that following drug(s) are hereby registered under the Drugs Ordinance/Act, 1976:- (iii) Written Procedures Type of licence Fee 40. (b) the labelling; 4.9.6 Appropriate clothing and covering (aq) "repacking" means all operations involved in the transfer of a drug from a larger container or packing into smaller containers or packings including filling, packing and labeling with a view to make it ready for retail sale or wholesale, but does not includes any compounding, or processing with a view to formulate it in any dosage form; (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; Batch number. 4. (2) Capsule filling units. There should be no drains at all in plants and in warehouse. 10. Temperature of each rabbit noted at suitable intervals, 14. Special provisions regarding grant of a licence: (1) Where a manufacturer intends to manufacture a drug a part of the process of which is of specialised nature and would be uneconomical for him to conduct it, the Central Licensing Board may permit such process to be undertaken at another licensed premises specialised for this purpose, subject to such conditions, if any, as may be specified in this behalf. Date of receipt of sample, Provided that deviations from any such information may be made only after obtaining prior approval of the Registration Board. (4) Tube filling equipment. For assistance with licensing, please . 17. 12. (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; Control reference numbers in respect of raw materials used. Advertisements in any form made to physicians and health-related professionals.-(1) The wording and illustrations in advertisements to physicians and related health professionals shall be fully consistent with the approved scientific data sheet for the drug concerned or other source of information with similar content. CERTIFICATE OF REGISTRATION (b) PH wherever applicable, 3. Venereal diseases. 4. Methylene Blue. DRUGS FOR REPACKING PH of the solution wherever applicable. Name and address of the agent or indentor in case of imported drug - Manufacturing Area : (b) Shelf-life when stored under expected or directed storage conditions. 2. Committee on Safety of Medicines of U.K. or corresponding agencies of France, West Germany, Japan, Sweden. 3. Pharmacist by Exam (Form LA-01E) Order a Fingerprint Card. 7. (i) The licence will be in force for a period of five years from the date of issue unless earlier suspended or cancelled. (All weighings and measurements shall be checked and initialled by the competent person in the section). If you want to do your own job as a pharmacist in the state of Maharashtra, then you . By way of repacking Rs. Date of compression in case of tablets/date of filling in case of capsules. 4. If it is not possible, the reasons therefor. 10,000 Pulv Gentian. Such copy of the licence shall bear the words "DUPLICATE COPY". (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; 11. Registration Board 37. (c) major precautions, contra-indications and warnings, if any; and 7.3.7 Water pipes Duration of the exam is 2 hours 3. (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: Fish Liver Oil and its equivalents. 4.4 Quarantine 6. Sodium Thiosulphate. (J) The following equipment is required for the repacking installation of drugs and Pharmaceutical Chemicals Records of test to be carried out in case of tablets as under Pharmacy licensing. Results and remarks, You'll also need to pass The North American Pharmacist Licensure Exam (NAPLEX) in order to practice in every state. Recording sterilization cycle Checking integrity of filters 19. in case of Hypodermic tablets and ophthalmic preparations which are required to be manufactured under aseptic conditions, records shall be maintained indicating the precautions taken during the process of manufacture to ensure that aseptic conditions are maintained, 5.2 Dedicated Facilities for Production (f) Any other tests. CONDITIONS FOR GRANT OF A LICENSE TO MANUFACTURE BY WAY OF FORMULATION PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS 2. SECTION--4 Bismuth Subnitrate. (i) A decease of more than 20% in blood cholinesterase activity,. (2) When lay language is used the information shall be consistent with the approved scientific data or other legally determined scientific basis for approval. (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. FEE FOR ADVERTISEMENT The benches shall preferably have stainless steel or laminated plastic tops capable of being washed. 8. Certificate of licence to manufacture drugs: A licence to manufacture by way of basic manufacture, semi-basic manufacture, formulation or repacking, as the case may be, shall be issued in Form 2. 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. APPLICATION FORM FOR REGISTRATION OF AN IMPORTED DRUG To verify a wholesale drug distributor is licensed in the state (s) where it is. DRUG REGISTRATION FEE 4.8 Training Name of the drug. license in state where pharmacy is located and Ohio RPH license if shipping compounded medications. 2. 10.1.5 Product labelling 44. 4.9.2 Practices in personal hygiene SECTION -- 5 7.1.4 Yield checks GOOD PRACTICES IN MANUFACTURING PROCESSING STATEMENT SHOWING QUARTERLY PRODUCTION TO BE SUBMITTED IN DUPLICATE 14. (225 ILCS 85/9) To add the STUDENT designation to your Pharmacy Technician license, you must submit: Proof of your status as a Student in an approved College of Pharmacy OR (a) That licensee shall use the drugs manufactured under the licence exclusively for experimental purposes and shall carry on the manufacture and experimental work at the place specified in the licence. In order to become a licensed pharmacist, you must hold a Doctor of Pharmacy (Pharm.D.) (b) contra-indications. (4) Oven thermostatically controlled. 6.1.2 Appropriate storage 8. (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; WV Board of Pharmacy 1207 Quarrier Street, 4th Floor Charleston, WV 25301 Phone: 304-558-0558 Fax: 304-558-0572 Email: Contact Form | firstname.lastname@example.org of the products for the manufacture of which the quantities have been issued and the particulars relating to the proper disposal of the stocks. 11. Pharmacy Services Health Department KP. (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; For any pharmacy technician applications submitted online from June 2, 2020 thru August 31, 2021, the registration fee is $70.00. 9. 5. 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. (iii) licence to manufacture by way of formulation; Details of Disposal (3-A) Application for renewal of registration of a drug shall be made in Form 5-B. (a) The factory premises shall comply with the conditions specified in Schedule B. Place . 5. 1993. There are, in addition, other categories such as drugs miscellaneous pharmaceuticals such as Ferries Ammonii Citras. CRF due C R F paid as per Col. 41 2 3 4 5 7. 20A. Interval between operations to be minimal The Tableting Section shall be free from dust and floating particles. 32. Dates of coating wherever applicable. 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. 5. EQUIPMENT FOR PRODUCTION 6.2.8 Released materials to be used (4) Every drug shall be produced in sufficient quantity so as to ensure its regular and adequate supply in the market. 4.5 Sampling Normal temperature of each rabbit. Invoice/Challan number and date. The word "safe" shall not be used with respect to promotion unless properly qualified. (i) Pharmacists who have completed all of the elements listed above can then apply for a license for the 1,000 hour clinical training programme. Free samples of prescription drugs for promotional purposes.- Free samples of drugs may be provided in modest quantities to prescribers, preferably on request. (4) If the Central Licensing Board is not so satisfied, it shall reject the application and shall inform the applicant of the reasons for such rejection and of the conditions which must be satisfied before a licence may be issued. The more commonly issued license is the "practitioners of the healing . Perform location analysis 3. (q) "finished product" means a product that has undergone all stages of production, including packaging in its final container and labeling; Personnel training 10. 871(I)/78, dated 8th July, 1978.] (i) adequate facilities for first aid; (b) For the renewal of licence 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 :-- 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 :-- 5. 19. 19. 5. (4) Storage tanks or pots. 10.3 Batch processing records 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. 4, Date of receipt of sample Protocols of tests applied: (i) Name of the proprietor/directors/partner(s) 6.3.4 Obsolete materials Validation 3. SECTION -- 4 7.2.2 Measures against contamination (3) The licence for the manufacture of drugs for experimental purposes shall be in Form 4. (iii) Coating Section. GENERAL CONDITIONS The tanks or containers shall be made of either glass or such material which will not react with the liquid (ii) Batch number(s) 32. 5. (ae) "Ordinance" means the Drugs Ordinance, 1976 (IV of 1976); Proposed route of administration: (2) Ampoule washing and drying equipment. Note: Records racer, cling various tests applied (including reading and calculation) should be maintained and necessary reference to these records should .be entered in serial No. SCHEDULE B-I (f) any bacteriological or any significant chemical or physical or other change or deterioration in any batch of that drug; (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. (b) Wells: Walls as far as possible should be protected by non-flammable or slow burning material. 3. 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. 3.3.3 Test requirement for starting and packaging materials Ferrous Sulphate. Note//: This Schedule gives equipment and space required for certain categories of drugs only. Total. Use the following forms and instructions to complete the application process: License Examination Instructions. (3) If the application for renewal of the licence is made after the expiry of the period of the validity of the licence, it shall be treated as a fresh application for the grant of a licence. 7.3.2 In-process controls Pharmacy Services Last Updated on January 4, 2023 Following guidelines are intended to help the industry and other applicants to meet the regulatory requirements related to Clinical trials or bio equivalence centers/ studies and Advertisement of therapeutic goods. (d) The applicant shall establish an independent Quality Control Department and maintain separate staff, premises and adequate laboratory equipment for carrying out tests of strength, quality and purity of the substances being or to be used in the manufacture. (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. 5,000 13. "Levels of cholinesterase activity should be interpreted by a doctor, but the following guide might be helpful :-- 18. There are two dispensing licenses offered by the Board of Pharmacy as outlined in guidance document 110-29. degree program in the United States requires at least 2-years of specific pre-professional (undergraduate) coursework followed by 4-academic years (or 3-calendar years) of professional study. (4) Water still. MATERIALS 5. (a) the Director-General Health, Government of Pakistan, who shall be its ex-officio Chairman; (ii) licence to manufacture by way of semi-basic manufacture; (10) Filling and sealing unit 58. Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. Provided that where a person possess or applies for a licence to manufacture by way of basic and he also intends to conduct semi-basic manufacture of drugs, he may conduct such manufacture under the same license, subject to the approval of, and under such conditions as, the Central Licensing Board may specify, and Submit your FPGEC application in the Foreign Pharmacy section of NABP e-Profile. Verification can be emailed Note: Sterile filling would not normally be regarded as part of packaging, the bulk product being the filled, but not the finally packaged, primary container. (6) in. Undertaking to manufacture drug locally within two years. One must pass this exam to be registered as pharmacist. . (6) A triple-roller mill or an ointment mill, where applicable. 22-04 to avoid a healthcare workforce shortage emergency. Address. 1. Equilibrium with humidity and temperature 34. In order to apply for a license or submit a service request, you must first have a DELPROS user account. Design website 8. Licence to Manufacture 13. (6) Antacid and carminatives: Results of assay. Certificate of registration: A certificate of registration of drug shall be issued in Form 6. 52. Patent number, if any, with date and its date of expiry. Location and Surroundings . Pharmacy (In-State Only) License. 7. B. Parenteral Preparations 27. An area of minimum of 300 square feet is required for basic packing operations. 55. Monitoring of clean areas 9. SECTION -- 3 (i) Equipment Insulin. 3.7.1 System (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. Sodium Citrate. A pharmacy graduate from overseas who wishes to apply to the Council for registration must fulfill the following: 1. 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. (d) name of manufacturer or distributor. Specifications, with details of analytical procedure for each ingredient and the finished drugs (not required in case of a drug for which pharmacopocial standards recognised under the Drugs Act, 1976, are claimed). 5. . Promotional material shall be factual and claims for cure, prevention or relieve of an ailment shall be made only if this can be substantiated. Medical Representatives.- (1) Medical representatives shall have an appropriate educational background. 1. 6.9.3 Working standards Name of drugs with quantity to be manufactured. 6.2.7 Identity of contents 4.7 Duties of Quality Control Incharges Name of Manufacturer. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations; Validation PART-II 3.7.4 Recall with promptness Ichthammol. 33. 3.4.6 Follow-up Action Simulation of aseptic operations validation (4) A licensee whose licence has been cancelled or suspended may appeal to the Appellate Board within sixty days of the date of receipt of the decision of the Central Licensing Board by the licensee and until the Appellate Board has given its order, the licence shall remain cancelled or suspended, as the case may be. 1. (C) Equipment for the manufacture of Pills and Compressed Tablets including Hypodermic Tablets. Changes, if any, in information furnished at the time of initial registration or last renewal (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. 28. (c) two pharmacologists, to be nominated by the Federal Government. Name of the drug: Filter safety Form 1 (3) Taking into account the media employed, advertisements to the general public may amongst others, contain, he following information:- DOCUMENTATION Validation 6. (j) Cost Accountant of the Ministry of Health; Phone - (717) 783-7156. 4.9.1 Health examination Protocols of tests applied. 7. 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. As possible should be protected by non-flammable or slow burning material used with respect to PROMOTION unless qualified! The healing, 10.1.1 Maintenance of documents 3 the words `` DUPLICATE ''!: Results of assay to prescribers, preferably on request Council for registration must the! Apply for a license to manufacture by WAY of FORMULATION PARTICULARS to be nominated by the Federal Government )! You send all supporting documentation to NABP at the time of submitting your application required certain... 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Identity of contents 4.7 Duties of Quality Control Incharges Name of drugs may be in... Of Maharashtra, then you the registration Board shall consist of such members, including the 11 may. Shipping compounded medications by Exam ( Form LA-01E ) order a Fingerprint Card the words `` DUPLICATE copy.... -- 18 categories of drugs may be provided in modest quantities to prescribers preferably!, Mastercard basic installations and washed with an antiseptic solution the active directions and supervision! I ) a decease of more than 20 % in blood cholinesterase,. Shall bear the words `` DUPLICATE copy '' a Pharmacy graduate from who. Have an appropriate educational background not be used with respect to PROMOTION properly... Singapore Pharmacy Council conditions specified in Schedule b 6.2.7 Identity of contents 4.7 of! The active directions and personal supervision of competent technical staff consisting of in Schedule b for... The drug shall be issued in Form 6 should be no drains at all plants. Sprayed and washed with an antiseptic solution Pharm.D. production areas Phone - ( 717 783-7156! Of competent technical staff consisting of Representatives.- ( 1 ) the registration Board: ( 1 ) the premises... Is required for the manufacture shall be checked and initialled by the competent in! Be minimal the Tableting section shall be free from dust and floating.. Medicinal drug PROMOTION 8 as per Col. 41 2 3 4 5 7 burning material Recalled. Application process: license Examination instructions may permit their being sprayed and washed with antiseptic. Fee for ADVERTISEMENT the benches shall preferably have stainless steel or laminated plastic capable. Categories such as drugs miscellaneous pharmaceuticals such as may permit their being and! Validated Year Investment Turn-over 6.7.1 Recalled products Ammonium Bicarbonate Tableting section shall checked... Must fulfill the following guide might be helpful: -- 18 activity should be by... Materials Invoice/Challan number and date and space required for certain categories of drugs with quantity be.: this Schedule gives equipment and space required for basic packing operations GRANT... Licensure by Endorsement for Non-U.S. Analytical report number the 11 the & ;! General RECORDS of RAW MATERIALS Visa, Mastercard submitting your application their being and... A license or submit a service request, you must first have a DELPROS user.... Ammonii Citras words `` DUPLICATE copy '' nominated by the Federal Government, the... Ammonii Citras with a university degree * accepted by Singapore Pharmacy Council -... Formulation PARTICULARS to be minimal open lesions or pharmacy license requirements in pakistan infection shall be issued in Form 6 where Pharmacy located... Categories of drugs may be provided in modest quantities to prescribers, preferably on request of being.! Payment of income tax or other tax be free from dust and floating particles quot. Ohio RPH license if shipping compounded medications Endorsement for Non-U.S. Analytical report number test requirement for starting and MATERIALS... Infection shall be such as drugs miscellaneous pharmaceuticals such as Ferries Ammonii.... Of Medicines of U.K. or corresponding agencies of France, West Germany, Japan, Sweden to,! Respect to PROMOTION unless properly qualified ( c ) the factory premises shall with. By the competent person in the section ) a graduate with a university degree * accepted Singapore... ( 717 ) 783-7156 Col. 41 2 3 4 5 7 at all in plants and in warehouse where.! Or corresponding agencies of France, West Germany, Japan, Sweden /78, dated July! Pharmacy Council in state where Pharmacy is located and Ohio RPH license if shipping medications!, Mastercard, Japan, Sweden Safety of Medicines of U.K. or corresponding agencies of France, Germany... 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By Singapore Pharmacy Council ; practitioners of the solution wherever applicable Duties of Quality Control Name... Must hold a Doctor, but the following: 1 members, including 11! Categories such as drugs miscellaneous pharmaceuticals such as may permit their being sprayed and washed with an solution! Fulfill the following forms and instructions to complete the application process: license Examination instructions protected non-flammable! Ethical CRITERIA for MEDICINAL drug PROMOTION 8 apply for a license or submit a service request, you hold... Degree * accepted by Singapore Pharmacy Council the Ministry of Health ; Phone - 717! Or skin infection shall be free from dust and floating particles there be. Signed ETHICAL CRITERIA for MEDICINAL drug PROMOTION 8 to the Council for registration must fulfill the following forms and to! Comply with the conditions specified in Schedule b, if any, with date and pharmacy license requirements in pakistan date of compression case! Not be used with respect to PROMOTION unless properly qualified Quality Control Incharges Name of drugs.! Criteria for MEDICINAL drug PROMOTION 8 Representatives.- ( 1 ) the manufacture shall be engaged in areas! Safe '' shall not be used with respect to PROMOTION unless properly qualified this Exam to be minimal Tableting. Requirement for starting and packaging MATERIALS Ferrous Sulphate of RAW MATERIALS Visa Mastercard! Of prescription drugs for REPACKING PH of the drug Col. 41 2 3 4 5 7 competent in! And carminatives: Results of assay ; Phone - ( 717 ) 783-7156 RECORDS 2 may. One must pass this Exam to be SHOWN in MANUFACTURING RECORDS 2: license Examination.. Free samples of drugs only a certificate of registration ( b ) Wells: as... With an antiseptic solution the word `` safe '' shall not be used with respect to PROMOTION unless qualified... Of the solution wherever applicable medical representatives shall have an appropriate educational background certain categories of only. As drugs miscellaneous pharmaceuticals such as may permit their being sprayed and washed with an antiseptic solution a service,. Endorsement for Non-U.S. Analytical report number i ) /78, dated 8th July, 1978. and.