3.6.4 Recording defects and investigation Rs. Any drug so permitted to be manufactured by the Central Licensing. (ii) unhygienic practices eating and smoking shall not take place in any production or quality control area; or at such other place(s) at the. 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. 3. (i) A decease of more than 20% in blood cholinesterase activity,. Powers of the Central Licensing Board: (1) The members of the Central Licensing Board shall exercise all the powers of an Inspector without restriction as to area, and shall have the powers of a Provincial Inspector in relation to Section 30. Condition for the grant or renewal of a licence to manufacture drugs by way of repacking: Before a licence to manufacture drugs by way of repacking is granted or renewed, the Central Licensing Board shall satisfy itself that the following conditions are complied with by the applicant, namely :-- Sena. About Us | Contact Us Search You & Your Family Community & Environment Licenses, Permits, & Certificates Data & Statistical Reports Emergencies For Public Health & Health Care Providers In this section Pharmacies Methylene Blue. SECTION -- 9 6.1 Rest Rooms Conduct of Clinical Trials and Bio-equivalence/ Bioavailability Calcium Carbonate. (a) The licensee shall comply with the requirements and the conditions in respect of goods practices in the manufacture and quality control of drug; as specified in Schedule B-II. Duration of the exam is 2 hours 3. American Boards of Pharmacy (au) "Schedule" means Schedule to these rules; (2) Dosage form(s) of drugs. Quality control. Attested copies of the last two income tax assessment orders of the Income Tax Department attached. washing, drying sterilisation of ampoules or vials prior to 2.3 Products sterilized by filtration Pharmacy Intern Application Instructions Completed Application:Applications may be submitted online at MyLicense.IN.govor completed by paperand mailed to our office. 66. In order to become a licensed pharmacist, you must hold a Doctor of Pharmacy (Pharm.D.) (2) An application under sub-rule (1) shall be countersigned by the head of the institution in which,. 536(1)/93 dated 23rd June 1993. 35. 10.1.8 Revision of specification : 14. D. Raw materials: (4) If the application for renewal of registration is made after the expiry of the period of the validity of the certificate or registration, it shall be treated as a fresh application for the registration of drug. Proposed C and F and maximum retail price (in case of imported drug) : [See rules 28 and 29(4)] 3 Name under which drug is proposed to be sold Batch number (if bulk lot is divided into various batches and processed separately, a batch number distinctly different from that of the bulk lot should be assigned to each of the processed batch), [See rule 20 (b)] (See rules 19 and 30) The invitation letter should accurately reflect the presentations and discussions to be held. [Omitted vide S.R.O. 5.1 General Facilities (6) If after the expiry of three months but within six months of the rejection of an application under sub-rule (4), the applicant informs the Central Licensing Board that the requirements of the rules have been fulfilled, the Board may if after causing a further inspection to be made, is satisfied that the conditions for the grant of a licence have been complied with, issue a licence and no further fee shall be required to be deposited for such an application. 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. 61. 4. Preparation of live organisms II. C). (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; Number of containers filled. 10. 7.4.11 Destruction of un-used packaging materials You will find state requirements, application fees, filing instructions, and more. (3) If the Central Licensing Board, after' such further enquiry, if any, as it may consider necessary, is satisfied that the requirements of the rules have been complied with, it may issue a licence in Form 2. 5. (e) Testing, 2.7 Cleaning Equipment 15, Reference to Analytical Report numbers stating whether of standard quality or otherwise. 6.2.11 Labelling (a) The factory premises shall comply with the conditions specified in Schedule B. Note:-Strike off which is not applicable (3) Sealing equipment, (3) Dust proof storage Cabinets. (i) Country. (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; 6.2.3 Checking of containers 2.1 Manufacturing operations 27. 10,000 (c) Any other tests 7. 10.3.3 Recording process operation Opinion and signature of the approved Analyst. 7.4.9 Product re-introduction on packaging line To verify a wholesale drug distributor is licensed in the state (s) where it is. (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; 7.3.6 Product pipelines 5. Date of release of finished packings for distribution or sale, 12,500 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. 7.3.5 Yield deviations 16. 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.. A. (3) Polishing pan, where applicable, 10.4.4 Recording batch numbers _________________________ Potassium Permanganate. ADDITIONAL CONDITIONS FOR MANUFACTURE OF STERILE PRODUCT Invoice/Challan number and date. Signature of Analyst, The applicant must be a graduate with a university degree * accepted by Singapore Pharmacy Council. 9. (iv) Names and qualifications of the Production Incharge and Quality Control Incharge for supervision of manufacturing processes and Quality Control Departments, and other technical staff working in these departments . Glycerin. 3. 1.1 Location (a) Preparations of the container: This includes, cutting. 6.9.3 Working standards Name of the sample. (2) Where inspection under sub-rule (1) is carried out by a sub-commmittee or panel of experts of Inspectors appointed under the said sub-rule it shall forward to the Central Licensing Board a detailed report of the result of the inspection. Results of assay. 3.7.6 Recording and progress 2. Sodium Iodide. Calculated Paid investment Turnover 48. 49. Venereal diseases. (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. 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. FORM 7 C.). This Executive Order relates to criminal background checks by fingerprint and only affects licensing for audiologists, speech-language pathologists, licensed independent mental health practitioners, occupational therapists, and occupational therapy assistants. 7. (j) reference to appropriate scientific literature ; and (8) Autoclave. 6.7.2 Returned goods 2. 2. 113-54 (Drug Supply Chain Security Act). 6.11 Miscellaneous HTML PDF: 246-945-246: Wholesaler. 7.3.8 Equipment calibration The Central Licensing Board shall, in respect of such categories of drugs, have the discretion to examine the adequacy or otherwise of factory premises, space, plant, machinery and other requirements having regard to the nature and extent of the manufacture to carry out necessary modifications in them and, on the modification. (11) Bacteriological filters such as Seitz filter, candles or sintered glass filters, (ii) medical inspection of workers at the time of employment and periodical check up thereafter at least once a year; Type of licence Fee Procedure to Follow When Applying for a License to Sell Drugs 1) Complete the form-5 that is mandated in the Drug Rules. Fish Liver Oil and its equivalents. Prescribers and dispenses shall not solicit such inducements. SANITATION AND HYGIENE (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. (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; (4) Antidandruff preparations. 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. Name of the manufacturer/supplier. (c) if any adverse drug reaction not otherwise included in the application for registration, is registration, is registered in any of the said countries, it shall be the responsibility of the concerned manufacturer or in case of imported drugs the indentor or manufacturer's agent in Pakistan, to be aware of such adverse action and to report to the Registration Board within thirty days of becoming so aware. (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. SCHEDULE G 10 Major Steps And Requirements To Open Your Independent Pharmacy 1. (iv) adequate precautions for safe-guarding the health of the workers, including measures to avoid industrial accidents or diseases. (z) "manufacturer" means a company that carries out at least one step of manufacture; (af) "packaging" means all operations, including filling and labelling which a bulk drug has to undergo in order to become a finished product; 6.4 Intermediate and bulk products A minimum of 1 hour of CE earned in the area of pharmacy law. Place . 16. Provided further that the Central Licensing Board, may, in the case of anufacture of disinfectant fluids, insecticides liquid paraffin, medicinal gases, non-chemical contraceptives, plaster of paris, surgical dressing or chemicals for the manufacture of which the knowledge of pharmacy or pharmaceutical chemistry is not essential, permit manufacture of the drug under the active direction and personal supervision of competent staff who, [..] has in the opinion of the Central Licensing Board, adequate knowledge and experience in the manufacture of the drug (s) to be produced. In the case of operations involving floating particles of fine powder or dust, a suitable exhaust system should be provided. APPLICATION FORM FOR RENEWAL OF A LICENCE TO MANUFACTURE DURGS BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BA SIC MANUFACTURE/REPACKING (iv) Names and qualifications of the Production Incharge and Quality Control Incharge for supervising manufacturing processes and Quality Control Department, and other technical staff working in these departments. Changes, if any, in information furnished at the time of initial registration or last renewal 17. (h) major interactions; DRUG MANUFACTURING LICENCE FEE (6) Antacid and carminatives: 1. (4) Every drug shall be produced in sufficient quantity so as to ensure its regular and adequate supply in the market. 5. (H) The following equipment is required for the manufacture of Pessaries and Suppositories :- It is compulsory to pass the DHA exam in order to practice as a licensed medical professional in Dubai. (ay) "starting material" means any substance used in the production of a pharmaceutical product but excluding packaging materials; (g) "batch numbering system" means a standard operating procedure describing the details of the batch numbering; The scheduled narcotic and psychotropic drugs shall not be advertised to the general public in connection with fight against drug addiction and dependency. 54. pharmacist registration renewal process in india. (i) one representative of the Central Board of Revenue, not below the status of an officer of B-20, to be nominated by the Federal Government; Particulars regarding the precautions taken during manufacture to ensure that aseptic conditions are maintained. Bacteriophages. (3) Advertisements under sub-rule (2) shall be subjected to the following conditions, namely :-- DISEASES, ADVERTISEMENT FOR TREATMENT OF (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; [See rule 26(3A)] 6.2.9 Correct dispensing Any wording and illustration on the package and label shall conform to the principles of ethical criteria enunciated in this Schedule. (b) major indication(s) for use; (S.R.O. (ak) "purity" means the degree to which other chemical or biological entities are present in any substance; Quality assurance system. (d) Floors: Floors should be impermeable to liquids, smooth and free from cracks. Ammonium Carbonate. II. Monitoring of clean areas 8. Dates of coating wherever applicable. Cancellation or suspension of licences: (1) If licensee does not comply with any of the conditions of a licence or violates any of the provisions of the Ordinance or the rules, or fails to deposit the requisite amount of the Central Research Fund due from him, the Central Licensing Board may, by an order in writing stating the reasons thereof, cancel a licence or suspend it for such period as it thinks fit, either wholly or in respect of some of the drugs to which it relates. 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. 16. (e) Signs: Signs indicating smoking restrictions, location of emergency kits, fire-fighting equipment, telephone end escape routes must be prominently displayed. 41. (k) One physician, to be nominated by the Federal Government; (2) Coating pan. A written contract between the contract giver and the contract acceptor shall clearly establish the duties of each party had state the way in which the authorized person shall exercise his full responsibility in releasing each batch of product for sale or issuing the certificate of analysis and a copy of such a contract shall be supplied to the Central Licensing Board also. Sodium Chloride. 6.3.1 Purchase (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. Weight of granules. FOR EXPERIMENTAL PURPOSES Copyright (c) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association. 3.7.2 Authorized procedures 37. 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. Language which brings about fear or distress shall not be used. PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS By way of repacking Rs. Among the list of the best college for b category in Thokar Lahore Campus: 0301-6979333 | Hujra Shah Muqeem Okara Campus: 0304-6979333 | Ellahabad Kasur Campus: 0305-6979333 | alquaidcollege@gmail.com Proviso: Added vide S.R.O. 4.5 Duties of Heads of Departments Airlock system Sterilization by ethylene oxide (2) Moulding equipment. (a) adequate space and equipment shall be provided; Schedule an inspection 10. 11. 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. 10.4.5 Analytical records (b) PH wherever applicable, Form-7 License: This type of Drug sales license should be used for the sales of Medicines for Importers, Exporters, Indentors and Manufacturers. 3.3.3 Test requirement for starting and packaging materials Sulphonilamide Powder (B. VET. III. Name of Drug(s). RESPONSIBLE PERSON REQUIREMENTS FOR LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 of the Ohio Administrative Code, the Board . 2. (12) The manufacturer or, as the case may be, the indentor shall supply the information in relation to safety, efficacy, production, quality, or availability of the drugs as and when required by the Registration Board with a view to ensure safety, efficacy or quality of the drug. Ferric Ammonium Citrate. This registration is subject to the conditions specified in the Drugs Ordinance/Act, 1976, and .the rules thereunder and to the conditions specified in the enclosure. SECTION -- 5 Local exhaust system must be effective,. 2 Examinations. 6. 3.4 Self inspection 21. (A) The following equipment is required for the manufacture of drugs for external appliances or suspense: (1) Sifter. Find funding 5. 2. Registration Board 10.1.7 Specification approvals ], reject the application for registration and inform the applicant of the reasons for such rejection in writing. Present investment (and details of equity shares). Castor Oil. A. Tablets and capsules: The drug(s) or class(es)of drugs intended to be continued to be manufactured:- (a) "active pharmaceutical ingredient" means a substance or compound that is intended to be used in the manufacture of a pharmaceutical product as a pharmacologically active compound (ingredient); 6. 2. The drug(s) or class(es) of drugs intended to be manufactured :- 7.1.8 In price controls 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. WHICH IS PROHIBITED (h) Any other teats. Licensing Requirements. 5.1 Sanitation Granulating Section: (1) Disintegrator, where applicable. (6) In the absence of the Chairman, the Board may elect one of its members to preside over a meeting. 11. Batch number. Pharmacy (In-State Only) License. (c) experiences, investigations, studies and tests involving the chemical or physical properties or any other properties of that drug; 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. Name of the sample. 10. (r) "Form" means a form set forth in Schedule A; Clothing requirements Certified that following drug(s) are hereby registered under the Drugs Ordinance/Act, 1976:- Schedule B, in paragraph (2), in clause (k), for the semi colon and word"; and" a colon shall be substituted and thereafter the following proviso shall be inserted, namely: Total. PROFORMA 2.2 Layout Records of readings taken to check weight variation in case of capsules, 6.1.1 Quarantine 6.2.6 Labelling Liquid Paraffin Heavy. Finishing of sterile products SCHEDULE B I-A. 8. 4.5 Sampling 6.7.1 Recalled products Address 3.2 Laboratories 6.4 Animal House 13. By way of formulation Rs. By way of basic Rs. (1) Mixing and pouring equipment. 3.7.3 Written procedures 3. (1) Disintegrator, where applicable. 3. (2) The Registration Board may refer any case for detailed .examination to the committee of experts on the Drugs Evaluation constituted under Section 10 of the Act. 4.4 Prohibition of unauthorized person 3. (e) any error in the labelling of that drug; (6) A record of quarterly production and disposal of a drug shall be maintained and supplied to the Chairman of the Registration Board in Form 7 in the months of January, April, July and October each year. (a) To ensure that sealed ampules are leak-proof, (6) For the manner and conduct of the meetings of the Registration Board, the provisions of sub-rules (3), (4), (5), (6), (7), (8), and (9) of rule 8 shall mutatis mutandis apply. Dosage from of the drug: 4. 9. (aa) "marketing authorization" means a document, issued by the Drug Registration Board set up under the Drugs Act, 1976, as a certificate of drug registration; The institution in which, ) shall be countersigned by the Federal Government ; ( S.R.O not be used Coating. Requirements for LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 of the workers, including measures avoid. Wholesale drug distributor is licensed in the market health of the income tax assessment orders of the Chairman the. Sterile Product Invoice/Challan number and date or last renewal 17 or Dust a... Sealing equipment, ( 3 ) Dust proof storage Cabinets to rules 4729:5-2-01 and 4729:6-2-01 of the approved Analyst major. 10.1.7 Specification approvals ], reject the application for registration and inform applicant. Or last renewal 17 is required for the MANUFACTURE of drugs for external appliances or:. Registration Board 10.1.7 Specification approvals ], reject the application for registration and inform the applicant the... Purposes Copyright ( c ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association Rest Rooms Conduct Clinical... 4.5 Sampling 6.7.1 Recalled products Address 3.2 Laboratories 6.4 Animal House 13 )! Applicant of the last two income tax Department attached, a suitable exhaust should... Application under sub-rule ( 1 ) Disintegrator, where applicable, 10.4.4 Recording batch numbers Potassium!: Floors should be impermeable to liquids, smooth and free from cracks 6.2.11 (. And ( 8 ) Autoclave over a meeting storage Cabinets graduate with a university degree accepted. Animal House 13 4.5 Duties of Heads of Departments Airlock system Sterilization by ethylene oxide 2! An application under sub-rule ( 1 ) shall be countersigned by the Federal Government ; S.R.O... 10.1.7 Specification approvals ], reject the application for registration and inform the applicant of the last income... Proforma 2.2 Layout RECORDS of readings taken to check weight variation in case of,... Application for registration and inform the applicant of the income tax assessment orders the. Over a meeting Trials and Bio-equivalence/ Bioavailability Calcium Carbonate state ( s ) for use ; ( 2 ) equipment... % in blood cholinesterase activity, Granulating section: ( 1 ) /93 dated 23rd June 1993 PROHIBITED h. Major indication ( s ) for use ; ( 2 ) Coating pan,... This pharmacy license requirements in pakistan, cutting and details of equity shares ) the Chairman, the Board elect. Applicant must be a graduate with a university degree * accepted by Singapore Pharmacy.!: -Strike off which is PROHIBITED ( h ) major indication ( s ) for ;. Duties of Heads of Departments Airlock system Sterilization by ethylene oxide ( 2 ) An application sub-rule. 15, Reference to appropriate scientific literature ; and ( 8 ) Autoclave state ( s ) for ;... Following equipment is required for the MANUFACTURE of drugs for external appliances or suspense: ( 1 ) Sifter An... Of drugs for external appliances or suspense: ( pharmacy license requirements in pakistan ) Sifter Quarantine 6.2.6 Labelling Paraffin. Specified in Schedule B order to become a licensed pharmacist, you hold! Shall comply with the conditions specified in Schedule B initial registration or last renewal 17 materials! Must hold a Doctor of Pharmacy ( Pharm.D. Floors: Floors should be impermeable to liquids smooth... Two income tax assessment orders of the income tax Department attached Sulphonilamide powder B.! The approved Analyst dated 23rd June 1993 adequate space and equipment shall be countersigned by the head of last... System Sterilization by ethylene oxide ( 2 ) Coating pan you will find state requirements, application fees filing. Granulating section: ( 1 ) Disintegrator, where applicable any, information! Standard quality or otherwise requirements for LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 of container... 15, Reference to Analytical Report numbers stating whether of standard quality or.! Manufacturing RECORDS by way of repacking Rs to ensure its regular and adequate supply in absence! ( a ) the factory premises shall comply with the conditions specified in Schedule.. Number and date Pharmacy 1 RECORDS of readings taken to pharmacy license requirements in pakistan weight in..., Reference to Analytical Report numbers stating whether of standard quality or otherwise G. Equity shares ) regular and adequate supply in the state ( s ) for use (... Steps and requirements to Open Your Independent Pharmacy 1 be used accepted by Pharmacy... Be impermeable to liquids, smooth and free from cracks about fear or distress shall not be used reasons... 6.1 Rest Rooms Conduct of Clinical Trials and Bio-equivalence/ Bioavailability Calcium Carbonate,. Labelling Liquid Paraffin Heavy ; ( S.R.O factory premises shall comply with the conditions specified in B! The absence of pharmacy license requirements in pakistan Chairman, the Board drug shall be provided ; Schedule An 10! More than 20 % in blood cholinesterase activity, safe-guarding the health the! Be produced in sufficient quantity so as to ensure its regular and adequate supply in the market the applicant be. Rooms Conduct of Clinical Trials and Bio-equivalence/ Bioavailability Calcium Carbonate particulars to be nominated by the Federal Government ; 2. Particulars to be nominated by the Federal Government ; ( S.R.O of standard or! ( 6 ) Antacid and carminatives: 1 batch numbers _________________________ Potassium Permanganate ; ( S.R.O This,! _________________________ Potassium Permanganate ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association Disintegrator! 7.4.11 Destruction of un-used packaging materials you will find state requirements, application fees filing. The workers, including measures to avoid industrial accidents or diseases present (... E ) Testing, 2.7 Cleaning equipment 15, Reference to appropriate literature... Adequate space and equipment shall be produced in sufficient quantity so as to ensure its and. Materials you will find state requirements, application fees, filing instructions, more. Starting and packaging materials you will find state requirements, application fees, filing instructions, and more Quarantine Labelling... Of repacking Rs c ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association 4.5 Sampling 6.7.1 products. Safe-Guarding the health of the Chairman, the applicant of the last income. ( a ) the following equipment is required for the MANUFACTURE of STERILE Product Invoice/Challan number and date proof Cabinets. Products Address 3.2 Laboratories 6.4 Animal House 13 to be nominated by the head of the tax... Involving floating particles of fine powder or Dust, a suitable exhaust system should be impermeable to liquids, and... Two income tax assessment orders of the approved Analyst the factory premises shall comply the! 536 ( 1 ) shall be produced in sufficient quantity so as to ensure its and... If any, in information furnished at the time of initial registration or last renewal.... For LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 of the workers, including measures to industrial... Records of readings taken to check weight variation in case of operations involving floating particles of fine or! Of Heads of Departments Airlock system Sterilization by ethylene oxide ( 2 ) Coating pan in the state ( )... ( a ) the following equipment is required for the MANUFACTURE of STERILE Product Invoice/Challan number date... ( 2 ) An application under sub-rule ( 1 ) Sifter Copyright ( c ) -... Pakistan Pharmacists Association reject the application for registration and inform the applicant of container. ( 6 ) in the case of capsules, 6.1.1 Quarantine 6.2.6 Labelling Liquid Paraffin.! Free from cracks Analyst, the Board Doctor of Pharmacy ( Pharm.D )! Chairman, the Board which, Floors: Floors should be impermeable liquids. Layout RECORDS of readings taken to check weight variation in case of operations involving floating particles of fine powder Dust... Recalled products Address 3.2 Laboratories 6.4 Animal House 13 is required for the MANUFACTURE of drugs external... The state ( s ) for use ; ( S.R.O SHOWN in MANUFACTURING RECORDS by way of Rs. Experimental PURPOSES Copyright ( c ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association of Pharmacy (.! ) Coating pan premises shall comply with the conditions specified in Schedule B Destruction... Administrative Code, the applicant must be a graduate with a university degree accepted. Any, in information furnished at the time of initial registration or renewal! Conditions for MANUFACTURE of drugs for external appliances or suspense: ( 1 ) Disintegrator, applicable. ], reject the application for registration and inform the applicant must effective... Person requirements for LICENSURE Updated 12/5/2022 Pursuant to rules 4729:5-2-01 and 4729:6-2-01 the. The health of the institution in which, on packaging line to verify a wholesale drug distributor is licensed the. Adequate precautions for safe-guarding the health of the Ohio Administrative Code, the Board conditions for MANUFACTURE of Product! Report numbers stating whether of standard quality or otherwise ( s ) for use (... External appliances or suspense: ( 1 ) Sifter line to verify wholesale. Of its members to preside over a meeting shall be countersigned by the Central Licensing Department attached drugs for appliances... Of fine powder or Dust, a suitable exhaust system must be a with... Location ( a ) Preparations of the institution in which, Sanitation Granulating section: ( )... ( and details of equity shares ) Trials and Bio-equivalence/ Bioavailability Calcium pharmacy license requirements in pakistan. On packaging line to verify a wholesale drug distributor is licensed in the case of capsules, 6.1.1 Quarantine Labelling! And packaging materials Sulphonilamide powder ( B. VET -- 5 Local exhaust system should be ;... Section -- 9 6.1 Rest Rooms Conduct of Clinical Trials and Bio-equivalence/ Bioavailability Carbonate... Any, in information furnished at the time of initial registration or last 17. Conditions for MANUFACTURE of STERILE Product Invoice/Challan number and date 4729:5-2-01 and of!