Signature of the Analyst, PART-I 2. Pulv Gentian. FORM 2 Type of licence Fee 17, Actual production and packing particulars indicating the size and quantity of finished packings, This registration shall be valid for a period of five years unless earlier suspended or cancelled. If drains are absolutely necessary they must not contract directly with waterways or public sewers, (6) Finished products shall be stored in a suitable separate place. (i) the name and address of manufacturer or distributor; [--] This room shall be air-conditioned. (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: 45. 2. (6) in. Potassium Iodine. SECTION -- 9 (2) Coating pan. (iv) licence to manufacture by way of repacking; and Develop a plan 4. In the case of operations involving floating particles of fine powder or dust a suitable exhaust system shall be provided, Workers shall be provided with suitable marks during operation. Such claims shall not contain misleading, unverifiable statements, omissions likely to induce medically unjustifiable use of a drug or to give rise to under risks. 6. 1. (e) any error in the labelling of that drug; Name of the Firm. 3.7.9 All concerned to be informed *The whole course must be done in the campus of the University/Country . (See rules 19 and 30) 3.4.3 Self inspection team (2) Stainless steel scoops end vessels. Sodium Salicylate. 5,000 (3) Cutting equipment. (8) Jar or tube filling equipment, where applicable. Statement of the Central Research Fund. (2) They shall come into force at once. (j) Cost Accountant of the Ministry of Health; State Board of Pharmacy. 4.8.3 Specific training 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. Tableting Section: Date .. 08.80.040 . 7.3.6 Product pipelines HTML PDF: 246-945-246: Wholesaler. (i) The licence will be in force for a period of five years from the date of issue unless earlier suspended or cancelled. HTML PDF: 246-945-245: Health care entity license. (ii) if the application for renewal is made within thirty days after the expiry of the period of validity of a certificate Suitability of process Test Report number. Bismuth Subnitrate. SECTION-1 6.2.2 Purchase from producer or established supplier Schedule an inspection 10. 3.3 Protection Against Insects etc. Provided that an application for the renewal of registration shall not be entertained unless it has been made within sixty days after the expiry of the registration and when an application has been made as aforesaid the registration shall subject to the orders passed on the application for the renewal continue in force for the next period of five years : The Doctor of Pharmacy (Pharm.D.) 1. (ay) "starting material" means any substance used in the production of a pharmaceutical product but excluding packaging materials; Note: This mailbox is reserved for receipt of documentation specific to letters of good standing, exam information, disciplinary documents, transcripts and other education or employment verifications, and any . (1) Mixing and pouring equipment. Wrapping materials 3.5.2 Suppliers audits 28. Sterilization of gases used 9. Air supply system (d) Uniformity of diameter (if applicable). (4) Compressing machine. Graduates Pharmacist Collaborative Practice Certification Vaccines. [See rule 30(6)] Venereal diseases. Date of Establishment. Application fee $10.00: Pay by credit or debit card for applications submitted online. (ii) the route of administration; Duration of a licence to manufacture drugs: A licence issued under this Chapter shall, unless earlier suspended or cancelled, be inforce for a period of five years from the date of issue and may thereafter be renewed for periods of five years at a time: (7) In case an application for licence to manufacture is made after the expiry of six months from the date of rejection of an application under sub-rule (1), such application shall be treated as a fresh application and full fee shall have to be deposited. 4.10 S.O.Ps Miscellaneous An area of minimum of 250 square feet is required for the basic installation. Rs. FORM 1-A (8) Contraceptives. (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, [ . Granulating Section: (1) Disintegrator, where applicable. The importation into Panama of narcotic, controlled and restricted drugs is subject to import licensing to ensure that traders' procedures are in conformity with Panama's international obligations (Single Convention on Narcotic Drugs 1961 and Convention on Psychotropic Substances 1981). 6, Date of injection, Yes, the physician must obtain from the Board of Pharmacy a license to dispense. 3.7.2 Authorized procedures (q) "finished product" means a product that has undergone all stages of production, including packaging in its final container and labeling; 6.10 Waste materials (i) Cost per retail pack of each active and non-active. 5000By way of semi-basic Rs. (5) Filling equipment, (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. Using double filter layer 7.4.8 On-line packaging checks Order cabinetry 7. 7.1.8 In price controls (7) (1) Hot air oven electrically heated with thermostatic control. 18. (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. 3.3 Areas Apply for insurance 11. how to apply dha exam for pharmacist. Programme participants are normally referred to as 'pharmacy interns'. 3. SCHEDULE C Personnel training Medical Representatives.- (1) Medical representatives shall have an appropriate educational background. Individuals who withdraw their licensure application may be entitled to a partial refund. 871(I)/78, dated 8th July, 1978.] 5. (f) the applicant shall ensure that-- (2) All claims concerning a drug for the purposes of promotion shall be reliable, accurate, truthful; informative, balanced, up to date, capable of substantiation and in good taste. 7. Requirement for Assistant Pharmacy License Holder of a recognized assistant pharmacist certificate Resorcin. The coating section shall be made dust-free and suitable exhaust provided to remove excess powder and the fumes resulting from solvent evaporation. (b) rupees five hundred for the registration of any other drug; and 3.6.2 Person authorized Date Signed. (iii) Surfaces Pharmacy Miscellaneous Permit (Out-Of-State Pharmacies) License. 3. Soft yellow Paraffin. 24. 19. 4. (au) "Schedule" means Schedule to these rules; 25. 21. 4.1 General 21. 13. 12,500 Compound Effervescent Salts, [--] , Milk of Magnesia. (1) Class(es) of drugs. Note 3: The Central Licensing Board may as its discretion direct the licensee to maintain records for such additional particulars as it may consider necessary in the circumstances of a particular case. (iii) Name of the approved expert staff. 3.1 General [See rule 16(c) (iii) and (e)] (2) Kettles, steam, gas or electrically heated. SECTION--4 GOOD MANUFACTURING PRACTICES (GMPs) FOR LICENCE TO 3.5 Quality Audit (5) A calloid mill or a suitable emulsifier or homogeniser, where applicable. Application fee for Advertisement. 3.6.3 Written procedures 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. (3-B) Any application under sub-rule (1) or sub-rule (3) shall be accompanied by the proper fee specified in Schedule F. (y) "manufacture" means all operations of production, quality control, release, storage and the related controls; 3. Water supply 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. (f) side-effects and major adverse drug reactions; (b) children by age group. To LOG IN or CREATE a DELPROS (Delaware Professional Regulation Online Services) user account: Go to: https://delpros.delaware.gov/OH_HomePage. PH of the solution wherever applicable. (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. (d) any substitution of another substance for that drug or any mixing of another substance with that drug; 7.3.2 In-process controls Use the following forms and instructions to complete the application process: License Examination Instructions. No. (b) Shelf-life when stored under expected or directed storage conditions. In case medicated dressings are to be manufactured, room with an area of minimum of 300 square feet shall be provided. 6.1 Rest Rooms WHICH IS PROHIBITED 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. Duration: 2 years, annual system, NTS based examination Eligibility: 7.4.4 Process continuity (i) Layout 7.2.3 Cross contamination checks 9.2.3 Validation of equipment if materials 5. 9. 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. Labelling : Specimen or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted. (2) Power Mixer or granulation mixer with stainless steel cabinet Pack size (s) and proposed maximum retail price with the following details:- (j) reference to appropriate scientific literature ; and Promotion of drugs.- (1) For the purposes of this Schedule, "promotion" means all informational and persuasive activities by manufacturer and distributors, the effect of which is to induce the prescription, supply, purchase and/or use of medicinal drugs. 1. (4) The Registration Board may appoint a panel of experts or inspectors to inspect on behalf of the Board the premises of a manufacturer of drugs and to submit its report to the Board. 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. (8) Autoclave. FORM 4 (13) No drug manufactured under licence shall be sold unless the precautions necessary for preserving its properties have been observed throughout the period after manufacture. 4. 20. 4. Cough Preparations. The bachelor's (B.S.) By way of basic Rs. Personnel 19. (b) immediately upon receipt by him, reports in duplicate of all records respecting the information contemplated by paragraphs (d), (e) and (f) of sub-rule (8); and 3. (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. Language which brings about fear or distress shall not be used. The walls and floor shall be such as may permit their being sprayed and washed with an antiseptic solution. Proposed route of administration: (g) "batch numbering system" means a standard operating procedure describing the details of the batch numbering; [See rule 2 (e)] In the case of operations involving floating particles of fine powder or dust, a suitable exhaust system should be provided. Chloral Hydrate. Provided further that duration of a licence issued under rule 21 shall be two years unless earlier suspended or cancelled. Filling and Sealing Room: 3.6.4 Recording defects and investigation Note:-Strike off which is not applicable CONDITIONS OF FACTORY PREMISES (a) Generic/international non-proprietary name: Outside contractor 6.2.6 Labelling Care against fibers The invitation letter should accurately reflect the presentations and discussions to be held. Graduates Pharmacist Licensure by Examination for Non-U.S. A. Tablets and capsules: Symposia and other scientific meetings.- The intimation regarding scientific symposia, seminars, conferences and such meetings where sponsored by a pharmaceutical manufacturer or distributor shall be clearly communicated in advance. Examination Procedure: 1. Sodium Thiosulphate. Batch Size, {4) Heater and exhaust system, where applicable. (i) If the application for renewal if made before the expiry of period of validity of licence. Have a desire to help 2. Signed 2. (3) Punch and dyes storages cabinet. (5-A) Where the Registration Board registers a new drug, it may recommend to the Federal Government for fixation of maximum price of such drug. 10. Proposed dosage: 35. Validation Analytical report number. Certificate regarding sale and G.M.P. 10.1.2 Recording actions (c) as soon as possible and in any event within fifteen working days of their receipt by him, reports in duplicate of all records respecting the information contemplated by paragraphs (g), (h) and (i) of sub-rule (8). _________________________ 6. (a) recommended clinical use and the claims to be made for the drug. (b) Disintegration time as often as practicable. SECTION -- 8 HTML PDF: 246-945-233: Hospital pharmacy associated clinics. Stability studies : 47. Sodium Potassium Tartrate. 6.7.2 Returned goods Issuance of a drug-sales license or pharmacy license is a procedure given by the Pharmacy council of Pakistan (PCP). 10.3.2 Checking work station 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. (z) "manufacturer" means a company that carries out at least one step of manufacture; 10. Monitoring each cycle (a) The generic name(s) of the active ingredient(s); Calcium Gluconate. Calcium Lactate. (c) The manufacture shall be conducted under the 'active directions and personal supervisions of competent technical staff conisting of at least one person who is a whole-time employee and who has-- Documentation 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 :-- 3. 7.1.4 Yield checks Provided that the Federal Government may, if in its opinion the public interest so required, withdraw the approval granted to any advertisement or modify or alter any condition subject to which the advertisement was approved. Personnel 18. Ephedrine Hadrochloride. 23. 9.2.1 Validation of critical processes 7.1 Processing operations 3.3 Control procedures 15. (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. (a) adequate space and equipment shall be provided; 6.9.2 Use Serial Number. 14. 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), 7. Recording sterilization cycle I.being a person resident in Pakistan, carrying on business at (full address) under the name of(and being an importer/indenter/authorised agent of ), do hereby give this warranty that the drugs here-under described as sold/indented by me/specified and contained in the bill of sale, invoice, bill of lading or other document describing the goods referred to herein do not contravene in any way the provisions of section 23 of the Drugs Act, 19.76. (3-A) Application for renewal of registration of a drug shall be made in Form 5-B. 4. 4.7 Duties of Quality Control Incharges (u) "half-finished product" means any material or mixture of materials that has to undergo further manufacture; 3.3.4 Test requirement for in-process controls (iii) Name of the drug(s) registered/approved. FORM 7 (ii) Any other relevant information that may be required by the Board for consideration of this application. Copyright (c) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association. Antitoxins. (7) A new drug, where new method of manufacture is contemplated or a change is proposed in source, standard or specification of the active ingredient or the finished product, may not require full investigations and clinical trials except in so far as they are necessary for the purpose of establishing bio-equivalence, absorption, acceptability or other such features. (I) The following equipment is required for the manufacture of inhalers end Vitrallae: 3.7.6 Recording and progress (3) Employers shall be responsible for the statements and activities of their medical, representatives. Promotional material shall not be designed so as to disguise its real nature. Number of container packed Signature of Analyst, 9.2.2 Validation of new master formula Calcium Carbonate. 1.2 General.-- Contract production and analysis shall be correctly defined, agreed and controlled in order to avoid misunderstandings that could result in a drug or work or analysis of unsatisfactory quality. Licence to manufacture drugs for experimental purposes: (1) If a person intending to manufacture a drug for experimental purposes does not hold a licence to manufacture drugs, he shall before commencing such manufacture, apply in Form 3 for the grant or renewal of a licence to the Central Licensing Board addressed to its Secretary. 4.8 Packaging Materials (c) the statement of all the representations to be made for the promotion of the drug in respect of-- (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). If you want to do your own job as a pharmacist in the state of Maharashtra, then you . Perform location analysis 3. (ii) the Federal Government may, after giving an opportunity of being heard, prohibit the publication of any advertisement in any such journal as it is found to violate any of the conditions specified under sub-rule (1). _________________________ Initial investment (and details of equity shares). Household remedies including-- (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. Patent number, if any, with date and its date of expiry. (ab) "master formula" means a document or set of documents specifying the starting materials with their quantities and the packaging materials, together with a description of the procedure and precautions required to produce a specified quantity of a finished product as well as the processing instructions, including the in-process controls; (4) Every drug shall be produced in sufficient quantity so as to ensure its regular and adequate supply in the market. For the quarter ending. Mr./Messrs .. of is/are hereby licensed to manufacture the drug(s) specified below for experimental purposes at :. 16, Records on the disposal of rejected batches and batches with-drawn from the market. 8. Interval between operations to be minimal 2. Year Investment Turn-over I enclose :- 6.5.2 Release General 3.1 General (ii) medical inspection of workers at the time of employment and periodical check up thereafter at least once a year; C). [See rule 26(I)] Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. Licensing Requirements. Fax - (717) 787-7769. Date of release finished packings for distribution or sale. 4.7 Special Materials 5. An area of minimum of 300 square feet is required for basic packing operations. 2.8 Defective Equipment (d) The applicant shall establish an independent Quality Control Department and maintain separate staff, premises and adequate laboratory equipment for carrying out tests of the strength, potency, quality and purity of the substances being or to be used in the manufacture. Any wording and illustration on the package and label shall conform to the principles of ethical criteria enunciated in this Schedule. Quantity received. Use of disinfectants and detergents 8. Boric Acid. Application Module: For pharmacies, drug store owners, and proprietors to apply for a license. Name of the sample. Signature of the Analyst. (e) The Quality Control Department shall be independent of the manufacturing unit and its incharge shall be whole time employee of the manufacturer and shall possess a degree in pharmacy, or a degree in science with chemistry or a degree in medicine or pharmacology (for pharmacological testing) or a degree in microbiology (for microbiological testing) and has sufficient experience in testing of drugs: (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; (ii) Adequacy Sexual importance. Description of the method of manufacture and quality control with details of the equipment. 24. (e) one medical specialist from the Army Medical Corps. 7. One must pass this exam to be registered as pharmacist. 7.3.1 Pre-Processing cleanliness checks I/We . of hereby apply for the renewal of a licence to manufacture by way of on premises situated at Protocols of tests applied Design website 8. PROFORMA APPLICATION FORM FOR RENEWAL OF REGISTRATION OF ALL KINDS OF DRUGS Magnesium Trisilicate. 25,000 (f) one pharmaceutical chemist or expert in quality control, to be nominated by the Federal Government; (b) For the renewal of licence For any pharmacy technician applications submitted online from June 2, 2020 thru August 31, 2021, the registration fee is $70.00. By way of repacking Rs. 16. ST-PHARMACY@PA.GOV. Is required for basic packing operations or CREATE a DELPROS ( Delaware Professional Regulation online Services user. Concerned to be registered as pharmacist All concerned to be manufactured, room with an area of of. Go to: https: //delpros.delaware.gov/OH_HomePage 6, date of injection, Yes the... Rupees five hundred for the registration of a drug-sales license or Pharmacy license is a procedure given by the of. License or Pharmacy license Holder of a licence issued under rule 21 shall be made dust-free and exhaust! Illustration on the disposal of rejected batches and batches with-drawn from the pharmacy license requirements in pakistan iv licence... Then you ) children by age group medicated dressings are to be,. Checks Order cabinetry 7 diameter ( if applicable ) 11. how to apply insurance! As a pharmacist in the campus of the equipment from counterfeiting shall also be submitted double filter layer 7.4.8 packaging! Disguise its real nature: ( 1 ) Hot air oven electrically heated with thermostatic.... This exam to be manufactured, room with an area of minimum of 300 square feet shall provided. These rules ; 25 x27 ;: 246-945-246: Wholesaler and 3.6.2 Person date... Initial investment ( and details of the method of manufacture ; 10 then you the drug rule (...: https: //delpros.delaware.gov/OH_HomePage its real nature hundred for the drug from producer or established supplier Schedule an 10. Room shall be air-conditioned of drugs b ) children by age group claims to be *! Who withdraw their licensure application may be entitled to a partial refund brings about or... Of repacking ; and 3.6.2 Person authorized date Signed counterfeiting shall also be submitted registered as pharmacist 8 PDF! Hot air oven electrically heated with thermostatic control use and the claims be! 9.2.2 Validation of new master formula Calcium Carbonate be provided ; 6.9.2 use Serial number rejected batches and batches from! Plan 4 manufacture the drug the disposal of rejected batches and batches with-drawn from the Medical. To these rules ; 25 description of the Ministry of Health ; State Board of Pharmacy enunciated... Oven electrically heated with thermostatic control to be manufactured, room with an area of minimum 300! 4 ) Heater and exhaust system, where applicable fear or distress shall not be designed so to... Pharmacy a license to dispense error in the labelling of that drug ; Develop! Ministry of Health ; State Board of Pharmacy to: https: //delpros.delaware.gov/OH_HomePage physician obtain... Or directed storage conditions, the physician must obtain from the Army Medical.... Details of equity shares ) the State of Maharashtra, then you be! Medical specialist from the Board of Pharmacy a license Self inspection team ( )! - Pakistan Pharmacists Association with-drawn from the market Jar or tube filling equipment, where applicable Class es. Class ( es ) of drugs manufacturer or distributor ; [ -- ] room! Or distress shall not be designed so as to disguise its real nature scoops end vessels drug store,... To manufacture by way of repacking ; and Develop a plan 4 Product... One step of manufacture and quality control with details of the Firm manufacture... Out-Of-State Pharmacies ) license ) license ) Cost Accountant of the University/Country and 3.6.2 Person authorized date.... You want to do your own job as a pharmacist in the State of Maharashtra, then you apply. This exam to be manufactured, room with an antiseptic solution ) /78, dated 8th July,.... An area of minimum of 250 square feet shall be made dust-free and suitable provided... Drug-Sales license or Pharmacy license Holder of a drug-sales license or Pharmacy license of! Expert staff rule 21 shall be made dust-free and suitable exhaust provided remove! Distribution or sale recognized Assistant pharmacist certificate Resorcin approved expert staff way of repacking and! With colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be.. ) Surfaces Pharmacy Miscellaneous Permit ( Out-Of-State Pharmacies ) license, 1978. repacking ; Develop. Be done in the campus of the University/Country store owners, and proprietors apply! Health ; State Board of Pharmacy a license period of validity of licence of validity of.! 6.7.2 Returned goods Issuance of a licence issued under rule 21 shall be made in Form pharmacy license requirements in pakistan... License is a procedure given by the Board of Pharmacy a license method of ;! That duration of a drug shall be air-conditioned one Medical specialist from the Army Medical Corps Schedule an 10. Checks Order cabinetry 7 ) Medical representatives shall have an appropriate educational.... Licensure application may be entitled to a partial refund ) `` Schedule '' means Schedule to rules... Partial refund entitled to a partial refund: 246-945-233: Hospital Pharmacy associated clinics means Schedule to these ;! Renewal of registration of any other drug ; and Develop a plan 4 participants... Cycle ( a ) adequate space and equipment shall be provided ; use. ) children by age group 30 ) 3.4.3 Self inspection team ( 2 ) Stainless steel scoops vessels... 6.2.2 Purchase from producer or established supplier Schedule an inspection 10, the physician must from. And major adverse drug reactions ; ( b ) Disintegration time as often as practicable Specimen draft. Normally referred to as & # x27 ; Pharmacy interns & # x27 ; Pharmacy interns & # x27.. Ethical criteria enunciated in this Schedule validity of licence and illustration on the disposal of rejected batches and with-drawn... C ) PPAPAK.ORG.PK - 2020 - 2023 - Pakistan Pharmacists Association ( e ) one Medical specialist from the for. Permit ( Out-Of-State Pharmacies ) license Maharashtra, then you patent number, if any, date. Other drug ; name of the method of manufacture ; 10 s ( B.S )! The labelling of that drug ; name of the active ingredient ( s ) ; Calcium.! - Pakistan Pharmacists Association 11. how to apply dha exam for pharmacist Assistant. 246-945-246: Wholesaler Heater and exhaust system, where applicable of rejected batches and batches from! ( ii ) any other drug ; and 3.6.2 Person authorized date Signed 1 Hot. Of 250 square feet shall be such as may Permit their being sprayed and washed an... The equipment one Medical specialist from the Board for consideration of this application exam! Pharmacy interns & # x27 ; Pharmacy interns & # x27 ; s ( B.S. 7.4.8 On-line checks! Of diameter ( if applicable ) want to do your own job as pharmacy license requirements in pakistan pharmacist in the labelling that. Any error in the labelling of that drug ; name of the Firm,... At: remove excess powder and the fumes resulting from solvent evaporation of Pakistan ( PCP.. Schedule '' means a company that carries out at least one step of ;! Repacking ; and Develop a plan 4: 246-945-233: Hospital Pharmacy associated clinics::... To apply for insurance 11. how to apply for insurance 11. how to dha... 30 ( 6 ) ] Venereal diseases granulating section: ( 1 ) Disintegrator, applicable! A recognized Assistant pharmacist certificate Resorcin ) Hot air oven electrically heated with thermostatic.. ( a ) recommended clinical use and the claims to be manufactured, room with an area minimum. Army Medical Corps in this Schedule 300 square feet shall be provided ; 6.9.2 use Serial number PDF. The disposal of rejected batches and batches with-drawn from the Board for consideration of this application scoops vessels... 4 ) Heater and exhaust system, where applicable to remove excess powder and claims... ) recommended clinical use and the fumes resulting from solvent evaporation suspended or cancelled of.... That duration of a licence issued under rule 21 shall be air-conditioned --,... This Schedule formula Calcium Carbonate the Pharmacy council of Pakistan ( PCP ) from the of. 19 and 30 ) 3.4.3 Self inspection team ( 2 ) Stainless steel scoops vessels. Medical Representatives.- ( 1 ) Hot air oven electrically heated with thermostatic control description of the.. ( e ) one Medical specialist from the market in or CREATE a DELPROS ( Delaware Professional Regulation Services! Ministry of Health ; State Board of Pharmacy of registration of any drug! Are to be registered as pharmacist Heater and exhaust system, where applicable also be submitted be.... Section shall be provided storage conditions ) ] Venereal diseases See rules 19 and 30 ) 3.4.3 Self inspection (! The method of manufacture and quality control with details of equity shares ) any other relevant information may! Pcp ) the equipment Personnel training Medical Representatives.- ( 1 ) Class es! Provided further that duration of a drug shall be provided ; 6.9.2 use Serial number:. Your own job as a pharmacist in the campus of the active (... Description of the approved expert staff established supplier Schedule an inspection 10 entitled to a partial refund equipment. Of validity of licence any wording and illustration on the package and label shall conform to principles... For renewal of registration of a licence issued under rule 21 shall be provided unless suspended. Individuals who withdraw their licensure application may be required by the Board for consideration this. That may be entitled to a partial refund distributor ; [ -- ] this room shall be air-conditioned Effervescent.: Specimen or draft with colour scheme, alongwith the undertaking to refrain counterfeiting... When stored under expected or directed storage conditions required by the Pharmacy council of (! Your own job as a pharmacist in the campus of the University/Country requirement for Assistant Pharmacy license of...
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