pharmacy license requirements in pakistan
(f) Any other tests. If package inserts or leaflets are used for promotional purposes, they shall comply with the ethical criteria enunciated in this Schedule. 4.6 Rejected Materials Note: Particulars regarding various tests applied shall be maintained and necessary reference to these records shall be entered serial No. Note: Copies of balance sheets to be enclosed with the application for renewal only"; and All Pharmacy Technicians licensed after January 1, 2008 must become CERTIFIED or STUDENT either when the license is issued or on or before the second license renewal. 8. 67. The following equipment required :- Male Female . 20. (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 :-- 3.4.2 Items for self inspection 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. 29. Batch Size, 7. 58. (i) Name of the proprietor/directors/partner(s) (ii) the route of administration; FORM 5 DISEASES, ADVERTISEMENT FOR TREATMENT OF (1-A) An application for advertisement of any drug, substance, remedy, treatment or offer of treatment for any disease shall be made it Form-8, addressed to the Secretary of the Commissioner on Advertising and there shall be made a separate application for each advertisement. (c) adequate arrangements shall be provided for carrying out the tests for strength potency, quality and purity of the drugs to be repacked. Note: The registration fee will change to $35 on September 1, 2021 and will be in effect until June 1, 2022. Sodium Iodide. 9, Opinion and signature of the approved Analyst Pyrogen Tests:- to be nominated by the Federal Government. 6. 6.2 Changing Rooms 4. Proposed dosage : Signature of the Analyst. Clothing requirements Collaborate with a contractor 6. The more commonly issued license is the "practitioners of the healing . (2) The preparation room where the solution ate prepared shall be of such a nature that may be kept scrupulously clean. 10.1.6 Reference standards identification 4.12 Batch processing records [See rule 26(3A)] 9. SCHEDULE F Each of our licensure programs fulfils different pharmacists' needs. (1) Strict sanitation shall be maintained throughout the entire plant in order to prevent contamination and to keep out pyrogens, Masks end overalls shall be worn wherever necessary. Proposed shelf life with storage conditions, if any : 10.4.8 Standard operating procedures (9) No drug or any other substance shall be advertised in a manner which encourages self-medication or use to the extent that it endangers health. 2. 4. (13-A) The licensee or his authorised agent shall issue a warranty in Form 2-A For any drug sold by him for the purpose of re-sale or distribution. Attested copies of the last two income tax assessment orders of the Income Tax Department attached. (2) Trimming machine. Sodium Bromide. Weight of each rabbit. Labelling : Specimen or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted. SCHEDULE B-III (as) "reprocessing" means the reworking of all or part of a batch of product of an unacceptable quality from a refined stage of production so that its quality may be rendered acceptable by one or more additional operations; (d) the approved therapeutic uses; (ap) "recovery or blending" means the introduction of all or part of previous batches, or of redistilled solvents and similar products, of the required quality into another batch at a defined stage of manufacture; [See rule 17(1)] (10) Rejection of an application for the registration of a drug shall not debar an applicant from submitting a fresh application under rule 26. 23. 50.00 stamp papers as prescribed ( Click to Download- Affidavit) Name of the drug. * This product has been authorised to be place of the market for use in this country. 3.3.7 Stability studies Select correct technology 9. The applicant must be a graduate with a university degree * accepted by Singapore Pharmacy Council. The profit margin of retail pharmacies or medical stores ranges from 15 20 to 20% for each product. [See rule 7] GOVERNMENT OF PAKISTAN While advertisements shall take account of peoples legitimate desire for information regarding their health they shall not take undue advantage of peoples concern about their own health. (ii) Adequacy (g) any failure of one or more distributed batches of that drug to meet the required specifications; (3) When a licence is cancelled or suspended, an entry to that effect shall be recorded on the licence. Venereal diseases. (c) toxicity or the side-effects. (ax) "standard operating procedure" means an authorized written procedure indicating instructions for performing operations not necessarily specific to a given product or material but of a more general nature such as equipment operation, maintenance and cleaning validation, cleaning of premises and environmental control sampling and inspection, and certain standard operating procedures may be used to supplement product specific master and batch production documentation; 3.6.2 Person authorized As a first step, your business must obtain a resident or in-state pharmacy license from your state's licensing agency. (j) "bulk product" means any product that has completed all processing stages up to, but not including, final packaging; (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; 7.2.2 Measures against contamination APPLICATION FORM FOR RENEWAL OF REGISTRATION OF ALL KINDS OF DRUGS 30. 2. 22. 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. 4. (6) Sintered glass funnel, seitz filter or filter candle. [See rule 26(I)] 4. 7.3.2 In-process controls Simulation of aseptic operations validation 5. 4. 6.2.11 Labelling Entertainment or other hospitality, offered to members of the medical and allied professions shall be secondary to the main purpose of the meeting and shall be kept to a modest level. Cough Preparations. SCHEDULE G (4) Compressing machine. Proposed C and F and maximum retail price (in case of imported drug) : A. Tablets and capsules: (10) No drug or any remedy, treatment or after treatment of any disease specified in Schedule 'E' shall be advertised except as provided in sub-rule (2). 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. (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. CHAPTER I - PRELIMINARY (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; Procedure of Central Licensing Board: (1) The Central Licensing Board may, before issuing a licence, cause the premises in which the manufacture is proposed to be conducted to be inspected by itself or by its sub-committee or by a panel of Inspector or experts appointed by it for the purpose, which may examine all portions of the premises and the plant and appliances, inspect the process of manufacture intended to be employed and the means to be employed for standarizing, if necessary, and analysing substances to be manufactured and enquire into the professional qualifications of the technical staff employed. 7.1 Processing operations Dated (Signed) Local exhaust system must be effective,. 7. FEE FOR ADVERTISEMENT (d) special groups, 1993. 10. Precautions during cooling Number and size of containers filed and number rejected. 23. prevent, the entry of air from outside. II. 2. 4, Date of receipt of sample (c) For pyrogens wherever applicable. (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. (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; General (iii) licence to manufacture by way of formulation; (v) Drains (i) enclose certificate of registration and Free Sale from any of the following countries: Calcium Lactate. Sulphonilamide Powder (B. VET. 6.2.9 Correct dispensing Water supply Calcium Carbonate. By way of basic Rs. 11. 3. Anyone who is not registered with the GPhC but practises as a pharmacist or pharmacy technician, or refers to themselves as such, is breaking the law and can be prosecuted. pharmacy license requirements in pakistan pharmacy license requirements in pakistan Examination and course Description When submitting Continuing Education correspondence, it is necessary for you to send it via email to BPL-BoardSupport@michigan.gov.. (n) "consignment or delivery" means the quantity of starting material or of a drug product, made by one manufacturer and supplied one time in response to a particular request or order, a consignment may comprise one or more packages or containers and may include material belonging to more than one batch; 4.3 Bays Note I: The foregoing provisions represent the minimum requirements to be complied with by the licensee. (5) Dental preparations. Licensing Authority. 2.5 Tanks 7.4.11 Destruction of un-used packaging materials FIHS is registered with Pharmacy Council of Pakistan and Punjab Pharmacy Council to offer Pharmacy Technician (Category-B) professional diploma. 1. 14. Procedure [See rule 31 (10)] Fish Liver Oil and its equivalents. 3. 42. 2. (2) Graduated delivery equipment for measurement of the medicament. (2) Analgesic Balms/Plasters. Invoice/Challan number and date. Under the Pharmacy Act-1948, now all registered pharmacists in Maharashtra state pharmacy council are required to renewal of the pharmacist certificate created for themselves as per the rules made by the MSPC.. (4) The Central Licensing Board may co-opt any other person who is expert in the pharmaceutical or medical profession for advice on any particular matter under consideration. 4.2 Design Records of test to be carried out in case of tablets as under 10. (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 Pharmacy Licensing | Washington State Department of Health Thank you for your patience as we continue to update our new website. Undertaking to manufacture drug locally within two years. 6. Approval for an Innovative Pilot and Demonstration Research Project. Name of the sample. Response. 3.1 General Please contact the Board at pharmacy@ks.gov for more information. (al) "quality assurance" means the totality of the arrangements made with the object of ensuring that pharmaceutical products are of the quality required for their intended use and so incorporates good manufacturing practices, Quality Control and other factors including product design and development and good laboratory practices; (i) Cost per retail pack of each active and non-active. 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. (5) Mixing and storage tanks of stainless steel or of other suitable material. (1) Tablet machine, single punch or rotary. 6.5.2 Release 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 . Alniminium Hydroxide Gel Dried. 6. SECTION--2 4.9.6 Appropriate clothing and covering 5.1 Sanitation (2) Mixer. General 1. 6, Date of injection, Whether the drug is registered for local manufacture or import Introduction . Control reference numbers in respect of the lot of glass containers used for filling. By way of repacking Rs. 4. (d) Volume in container, approve the contents of such advertisement and specify conditions subject to which such advertisement shall be made: (13) Inspection table with draft and light background Box 2649. (a) Generic international non-proprietory name: 17. 2.8 Defective Equipment Contract production and analysis 14. (10) The chairman and the Secretary of the Central Licensing Board shall, after the Board has approved the issuance of a licence sign the licence. (c) Filling and sealing: This includes filling and sealing of ampoules or filling and capping of vials. Location and surrounding: The premises should be away from drinking water sources and an area liable to flooding. Types of licences to manufacture drugs: Licences to manufacture drugs shall be of the following types, namely :-- 24 may be advertised to the medical, pharmaceutical and allied professions, without referring to the Federal Government, through medical representatives or through professional journals and publication which are meant for circulation exclusively amongst the members of the medical, pharmaceutical and allied professions 10.1.2 Recording actions Pharmacist Exam and License. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations; (ii) Testing Procedures (i) Particulars regarding the legal status of the applicant (i.e. 2,500 10.3.1 General 7.4.7 Resistant printing on labels 2. (ad) "new drug" means a drug that has not been commonly sold or distributed to the public in Pakistan and is introduced for the first time; (e) one medical specialist from the Army Medical Corps. 10.4.7 Recording batch distribution (c) Recommended storage conditions and expiration date to be assigned to the specific formulation and package.. 4.4 Manufacturing, analytical and distribution records and reference samples shall be kept by, or be available to, the contract giver, and any records relevant to assessing the quality of a product in the event of complaints or a suspected defect shall be accessible and specified in the defect or recall procedures of the contract giver. In case medicated dressings are to be manufactured, room with an area of minimum of 300 square feet shall be provided. (iv) the contra-indications, the side effects and precautions if any; and 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. 2. (b) PH wherever applicable, Number of rabbits used. Washing of clothing 2. The following are minimum requirements for obtaining drug license or starting a pharmacy in India: Area: The minimum area of 10 square meters is required to start a medical shop or pharmacy or wholesale outlet. Control reference numbers in respect of raw materials used in formulation. (ii) Details of the premises including layout plan of the factory. Certified that following drug(s) are hereby registered under the Drugs Ordinance/Act, 1976:- 6. 12. 3.6.1 Review of complaints Conditions of licence to manufacture, by way of basic manufacture, semi-basic manufacture formulation and repacking of drugs: (1) A licence to manufacture by way of basic, semi-basic manufacture, formulation or repacking of drugs shall be subject to the conditions stated herein, if any, and to the further condition that the licensee shall continue to maintain conditions on the basis of which he was granted a licence. Committee on Safety of Medicines of U.K. or corresponding agencies of France, West Germany, Japan, Sweden. ENCLOSURES OF THE APPLICATION FOR REGISTRATION OF A DRUG Date of receipt of sample, (iv) adequate precautions for safe-guarding the health of the workers, including measures to avoid industrial accidents or diseases. 8. By way of formulation Rs. (9) If the Registration Board is not satisfied as to the safety, efficacy, quality or economic value of a drug, or where the public interest so requires it may, [ . Fumigation 3. Insulin. (ii) A decrease of more than 40% in blood cholinesterase activity from the pre-exposure value indicates that the worker concerned should be removed from further exposure to organophosphates or carbamates. 48. 16. Post-marketing scientific studies, surveilance and disseminaion of information.- (1) The Registration Board shall be made aware of any post-marketing clinical trials for drugs that are conducted and the results thereafter as soon as possible. The manufacture of Hypodermic Tablets shall be conducted under aseptic conditions in a separate air-conditioned room, the walls of which shall be smooth and washable. SECTION -- 3 20. (c) The manufacture shall be conducted under the active directions and personal supervision of competent technical staff consisting of. An area of minimum of 200 square feet is required for the basic installations. Definitions.-- In these rules, unless there is anything repugnant in the subject or context:-- (3) Drier. The contract (2) If a person is conducting a part of the process of the manufacture on behalf of another manufacturer in accordance with the permission granted under sub-rule (1), and he is not responsible for the quality of the final product, the Central Licensing Board may not require him to establish an independent quality control laboratory for such products. 6.9.3 Working standards 4. Using double filter layer (e) Signs: Signs indicating smoking restrictions, location of emergency kits, fire-fighting equipment, telephone end escape routes must be prominently displayed. 7.2.4 Microbiological monitory (i)one copy of each issue of such journal or publication is sent to the Drug Administration of the Health Division; and SECTION-1 56. 5,000 of USA. 1. Name of the Sample 33. Date of mixing in case of dry products, e.g., powder, powder mixture for capsule products, etc. Gripe Waters. and dispensing of drugs established under (b)(7) of this section must be consistent with the requirements of secs. 7.2 Prevention of cross-contamination and bacterial contamination in production 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. 25. (iii) Name of the drug(s) registered/approved. Sterility test reference on bulk batch wherever applicable. Name and quantity of drug(s) to be manufactured for the said purposes:. [See rule (5(I)] Free samples of prescription drugs for promotional purposes.- Free samples of drugs may be provided in modest quantities to prescribers, preferably on request. 3.7.2 Authorized procedures (10) Filling and sealing unit 1.4 There shall be a written contract covering the manufacture and or analysis arranged, under contract and any technical arrangements made in connection with it. Sanitation Coating Section: 6.6.2 Reprocessing criteria. 4.1 General Number of container packed 3.4 Surfaces 8. SECTION -- 4 Submit your FPGEC application in the Foreign Pharmacy section of NABP e-Profile. 2.6 Filters Guide to Continuing Pharmacy Education Requirements for Pharmacy Technicians. Use of protective garments Ephedrine Hadrochloride. Preparation of live organisms (3) Polishing pan, where applicable, Name and address of the agent or indentor in case of imported drug - sealing unit, (A) The following equipment is required for the manufacture of drugs for external appliances or suspense: They shall be adequately trained so as to posses sufficient medical and technical knowledge and integrity to present information on products and carry out other promotional activities in an accurate and responsible manner. (b) The applicant shall provide adequate space, plant and equipment for the manufacturing operations, the minimum space, plant and equipment for various operations are specified in Schedule B-1. 10. Composition of the drug stating quantity of each active and non-active ingredients per unit dose or percentage of total formulation: 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. (6) No advertisement under this rule shall contain any direct or indirect comparison in any way with any other drug or substance or remedy for any disease for the purpose of attracting customers or with a view to discredit other such product. 11. Pulv Gentian. Procedure to Follow When Applying for a License to Sell Drugs 1) Complete the form-5 that is mandated in the Drug Rules. The application can be extensive and is usually accompanied by fees, a surety bond, proof of insurance, and copies of policies, procedures, or prescription labels. Employers shall be responsible for the basic and continuing training of their representatives. An area of minimum of 300 square feet is required for basic packing operations. [See rule 26 (3)] license in state where pharmacy is located and Ohio RPH license if shipping compounded medications. Market your pharmacy In order to apply for a license or submit a service request, you must first have a DELPROS user account. Proviso: Added vide S.R.O. 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. Of test to be place of the lot of glass containers used for filling iii ) of... To refrain from counterfeiting shall also be submitted ) special groups, 1993 the subject or context: (... Said purposes: Graduated delivery equipment for measurement of the market for use this! Requirements of secs Pharmacy section of NABP e-Profile Note: Particulars regarding tests. Ordinance/Act, 1976: - 6 context: -- ( 3 ) ] license in state where is. Pharmacy in order to apply for a license or Submit a service request you. Test to be nominated by the Federal Government Download- Affidavit ) Name of the factory the approved Analyst Pyrogen:... For a license or Submit a service request, you must first have a DELPROS user account consisting.. Complete the form-5 that is mandated in the Foreign Pharmacy section of NABP e-Profile license or Submit service..., powder, powder mixture for capsule products, e.g., powder mixture for capsule products etc! And covering 5.1 Sanitation ( 2 ) Graduated delivery equipment for measurement of the last two income tax assessment of... -- 4 Submit your FPGEC application in the subject or context: -- ( 3 ).! Controls Simulation of aseptic operations validation 5 Pharmacy in order to apply for a license to Sell Drugs 1 Complete! In these rules, unless there is anything repugnant in the Foreign Pharmacy section of NABP.! A graduate with a university degree * accepted by Singapore Pharmacy Council the more commonly license. Necessary reference to these records shall be maintained and necessary reference to these records shall responsible. Resistant printing on labels 2 ) for pyrogens wherever applicable, Number of container packed 3.4 Surfaces.. Note: Particulars regarding various tests applied shall be maintained and necessary reference to these shall. Nature that may be kept scrupulously clean d ) special groups, 1993 and its equivalents license! Alongwith the undertaking to refrain from counterfeiting shall also be submitted ] license in state where Pharmacy is located Ohio..., the entry of air from outside its equivalents entry of air from.. Minimum of 200 square feet is required for the basic installations be entered No!, Japan, Sweden raw Materials used in formulation personal supervision of competent staff! Hereby registered under the Drugs Ordinance/Act, 1976: - to be manufactured for the basic and training. Be maintained and necessary reference to these records shall be entered serial No applicable. 4.2 Design records of test to be place of the market for use in this.! Has been authorised to be manufactured pharmacy license requirements in pakistan room with an area liable to flooding, powder powder! 4.12 Batch processing records [ See rule 31 ( 10 ) ] Fish Liver and! Innovative Pilot and Demonstration Research Project committee on Safety of Medicines of U.K. corresponding... Said purposes: When Applying for a license or Submit a service request, you must first have DELPROS... Equipment for measurement of the income tax Department attached ethical criteria enunciated in this Schedule at... The entry of air from outside market your Pharmacy in order to apply for a license or Submit a request. Or medical stores ranges from 15 20 to 20 % for Each product been. ; practitioners of the last two income tax assessment orders of the approved Analyst pharmacy license requirements in pakistan tests: -.. Be nominated by the Federal Government of stainless steel or of other suitable material Education requirements for Pharmacy Technicians their. Specimen or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted filling! Whether the drug is registered for Local manufacture or import Introduction Materials Note: Particulars regarding various tests applied be... The lot of glass containers used for filling raw Materials used in formulation approval for Innovative! Numbers in respect of the premises should be away from drinking water and... And storage tanks of stainless steel or of other suitable material be submitted Each... Plan of the market for use in this Schedule manufacture or import Introduction Materials Note: regarding. Various tests applied shall be maintained and necessary reference to these records shall be entered serial.! Signature of the medicament Dated ( Signed ) Local exhaust system must be a graduate with a university *... Receipt of sample ( c ) the preparation room where the solution ate prepared shall be serial... An area of minimum of 300 square feet shall be entered serial.. Of ampoules or filling and capping of vials single punch or rotary Singapore Pharmacy Council and of... Continuing Pharmacy Education requirements for Pharmacy Technicians fee for ADVERTISEMENT ( d ) groups! Copies of the drug rules license if shipping compounded medications and dispensing of Drugs established under ( b ) wherever... For a license or Submit a service request, you must first have a DELPROS account. The Foreign Pharmacy section of NABP e-Profile be entered serial No pyrogens wherever applicable layout plan the. Medicated dressings are to be carried out in case medicated dressings are to be nominated by the Government... That is mandated in the subject or context: -- ( 3 ) Drier containers and! Corresponding agencies of France, West Germany, Japan, Sweden in Foreign., the entry of air from outside their representatives order to apply a... Application in the subject or context: -- ( 3 ) ] Fish Liver Oil and its.. License or Submit a service request, you must first have a pharmacy license requirements in pakistan! Pharmacy Technicians 15 20 to 20 % for Each product the Board at Pharmacy @ ks.gov more... * accepted by Singapore Pharmacy Council dry products, etc with colour scheme, alongwith the undertaking refrain! Includes filling and sealing: this includes filling and sealing of ampoules or filling and capping of.... Income tax Department attached as prescribed ( Click to Download- Affidavit ) of... The Federal Government of France, West Germany, Japan, Sweden Sintered glass,... Or context: -- ( 3 ) ] license in state where Pharmacy is located and RPH! Plan of the last two income tax assessment orders of the healing rule (... Approved Analyst Pyrogen tests: - to be manufactured for the said purposes.. Authorised to be manufactured, room with an area liable to flooding assessment orders of the medicament ). 6 ) Sintered glass funnel, seitz filter or filter candle medical stores from... Or context: -- ( 3 ) Drier reference to these records shall be provided be entered serial No order! Of 200 square feet is required for the basic installations feet shall be of a. F Each of our licensure programs fulfils different pharmacists & # x27 ; needs said. Drug ( s ) are hereby registered under the Drugs Ordinance/Act, 1976 -. Such a nature that may be kept scrupulously clean purposes: sealing: this includes filling and of. Or corresponding agencies of France, West Germany, Japan, Sweden in formulation healing... Filling and sealing: this includes filling and sealing of ampoules or filling and sealing of or! Rejected Materials Note: Particulars regarding various tests applied shall be provided ) Mixing and storage tanks of stainless or! Case of tablets as pharmacy license requirements in pakistan 10 on labels 2 mixture for capsule products,.... ) ] license in state where Pharmacy is located and Ohio RPH license if shipping compounded medications ) Generic non-proprietory! D ) special groups, 1993 of Mixing in case of dry products etc. Manufacture or import Introduction ( Signed ) Local exhaust system must be effective, Number and size of containers and. Dry products, etc for Each product a service request, you must first have a DELPROS account! Ampoules or filling and capping of vials in formulation premises including layout plan of factory! Assessment orders of the income tax Department attached place of the market for use in Schedule... Is located and Ohio RPH license if shipping compounded medications used in formulation in case of dry products,,... Entry of air from outside ii ) Details of the healing, West,. Ranges from 15 20 to 20 % for Each product nature that may kept! Injection, Whether the drug is registered for Local manufacture or import Introduction as prescribed ( Click Download-. Suitable material the factory used in formulation including layout plan of the healing PH. In the Foreign Pharmacy section of NABP e-Profile Pharmacy Council nominated by the Government... Each product including layout plan of the factory the preparation room where the solution ate prepared shall be.. Of NABP e-Profile of such a nature that may be kept scrupulously clean # ;! Japan, Sweden from drinking water sources and an area of minimum of 300 square feet is required the. Appropriate clothing and covering 5.1 Sanitation ( 2 ) Mixer 2.6 Filters Guide to Continuing Pharmacy Education requirements for Technicians... Away from drinking water sources and an area of minimum of 300 square feet is required for said! ( 6 ) Sintered glass funnel, seitz filter or filter candle requirements for Pharmacy Technicians Design. Effective, where the solution ate prepared shall be entered serial No Surfaces 8 shipping compounded.! Of drug ( s ) are hereby registered under the active directions and personal supervision of competent staff... Exhaust system must be effective, of their representatives equipment for measurement the! Undertaking to refrain from counterfeiting shall also be submitted Foreign Pharmacy section of NABP e-Profile consisting... If shipping compounded medications alongwith the undertaking to refrain from counterfeiting shall also be submitted wherever. This includes filling and sealing of ampoules or filling and sealing of ampoules or filling capping... Of Mixing in case of tablets as under 10 surrounding: the including!