(4) Oven thermostatically controlled. 14. (3) A suitable power driven mixer. (an) "quarantine" means status of starting or packaging materials intermediate, or bulk or finished products isolated physically or by other effective means while a decision is awaited on their release, rejection, or reprocessing; (at) "returned product" means finished product sent back to the manufacturer or distributor; (E) The following equipment is required for filling of Hard Gelatin Capsules:- 14. By way of repacking Rs. How to get a pharmacy license in Pakistan? Date of compression in case of tablets/date of filling in case of capsules. Caffein and its Salts. 34. (2) Capsule filling units. Collaborate with a contractor 6. Number and size of containers filed and number rejected. (b) Disintegration time as often as practicable. Pharmacy Services Last Updated on January 4, 2023 Following guidelines are intended to help the industry and other applicants to meet the regulatory requirements related to Clinical trials or bio equivalence centers/ studies and Advertisement of therapeutic goods. (3) Name of the drug(s). Sodium Bromide. (1) Tablet machine, single punch or rotary. 5. 2. 6.1 Rest Rooms 4, Date of receipt of sample. 4.5 Duties of Heads of Departments "Levels of cholinesterase activity should be interpreted by a doctor, but the following guide might be helpful :-- Quality control. (3) Sealing equipment, 3. 536(1)/93 dated 23rd June 1993. (12) The licensee shall on being informed by the Central Licensing Board or a Provincial Quality Control Board that any part of any batch of a drug has been found not to conform with the requirements of the Ordinance or the rules and on being directed so to do, withdraw the remainder of the batch of such drug from sale and, so far as may in the particular circumstances of the case be practicable, recall all issues already made from that batch and dispose it of in such manner as may be directed by the said Board. Phenothlazine (B. VET. Serious illness liable to endanger the life of the patient (e.g., pneumonai, pleurisy, abscess of the lungs). (7-A) The indenter, importer or manufacturer's authorised agent shall issue a warranty in Form 2-A for any drug indented or sold by him for the purpose of re-sale or distribution; and (3) Substantiated information on hazards associated with the drug shall be reported to the Registration Board as a priority. Calculated Paid investment Turnover I enclose :- In package inserts or leaflets the manufacturers or distributors shall ensure that the information reflected is correct. Licence to Manufacture (d) any substitution of another substance for that drug or any mixing of another substance with that drug; SCHEDULE G 25. Name of drugs with quantity to be manufactured. SECTION--3 4. Sodium Iodide. Fumigation (c) rupees two hundred and fifty for the renewal of the registration of a new or any other drug: (4) Filling equipment. An area of minimum of 300 square feet is required for the basic installations. General 4.4 Quarantine FORM -5(A) 10.4.2 Pre-packaging line checks Ichthammol. General (3) Polishing pan, where applicable, 2.1 The contract giver shall be responsible for assessing the competence of the contract acceptor in successfully carrying out the work or tests required and for ensuring by means of the contract that the principles of good manufacturing practices are followed. Monitoring of clean areas 3.7.1 System Results and remarks, (225 ILCS 85/9) To add the STUDENT designation to your Pharmacy Technician license, you must submit: Proof of your status as a Student in an approved College of Pharmacy OR 4.9.2 Practices in personal hygiene 17. Pharm.D. (7) The Central Licensing Board may authorise the Chairman to any of its members to perform any specific function of the Board for a specified period. (1) Mixing and pouring equipment. 6 wherever necessary. PROFORMA 277 (1)/96 dated 2 lst April 1996. Language which brings about fear or distress shall not be used. 2. Visa, Mastercard. in Pharmacy. Registration Board: (1) The Registration Board shall consist of such members, including the 14. (15) Labelling and packing benches, (i) if the application for renewal is made before the expiry of the validity of a certificate Rs. ADDITIONAL CONDITIONS FOR MANUFACTURE OF STERILE PRODUCT 4 5 6 7 (4) Folding and pressing machine for gauze. Sterilization by radiation Wrapping materials 12. in the country of origin (in English and in Form 5 (c) : 6.1.2 Appropriate storage Sterility testing 17. Methylene Blue. 19. Serial number (iv) licence to manufacture by way of repacking; and Use of disinfectants and detergents (ii) Adequacy 4.2 The contract shall specify the way in which the authorized person releasing the batch for sale ensures that each batch has been manufactured in, and checked for, compliance with the requirements of the marketing authorization. Compound Effervescent Salts, [--] , Milk of Magnesia. Proposed route of administration: Manufacturing Area : General (a) Generic international non-proprietory name: Batch number. Name, address and status of the applicant: (16) Storage equipment including cold storage and refrigerators, if necessary Personnel training If drains are absolutely necessary they must not contract directly with waterways or public sewers, 3. Sodium Potassium Tartrate. (2) Dosage form(s) of drugs. The Ministry of Health and Family Affairs issued the Cosmetic Rules in December 2020, which states that a drug license is mandatory for importing cosmetics into India. 7.4.7 Resistant printing on labels 08.80.040 . (c) Any other tests (c) experiences, investigations, studies and tests involving the chemical or physical properties or any other properties of that drug; approve the contents of such advertisement and specify conditions subject to which such advertisement shall be made: Number of mice used and weight of each mouse, Strength and volume of the drug injected, 5 whenever necessary. We offer Coaching for Healthcare professionals under the guidance of well experienced professional trainers. 145 (I)/76 dated 12th February 1976:- In exercise of the powers conferred by Section 41 of the Drugs Ordinance, 1976 (IV of 1976), the Federal Government is pleased to make the following rules, namely :-- Schedule an inspection 10. 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. (a) Generic/international non-proprietary name: 13. in force for a period of five years from the date of Registration of the drug and may thereafter be renewed for periods not exceeding 5 years at a time. 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. This registration shall be valid for a period of five years unless earlier suspended or cancelled. Procaine Hydro-Chloride. (ii) unhygienic practices eating and smoking shall not take place in any production or quality control area; 8. (g) Toxicity test, wherever applicable. 10.2 Specification for intermediate and bulk products 7. 5000By way of semi-basic Rs. 2.1 General 4. 9. (14) Leak tasting equipment. 33. 7. 3.2 Laboratories 4.2 Specification & Testing Procedures Quantity received. 4. 43. (i) enclose certificate of registration and Free Sale from any of the following countries: (c) Uniformity of weight. (3) Reminder advertisements shall include, amongst others, at least the international non-proprietary name or generic name, the name of each active ingredient and the price of drug and the name and address for the manufacturer or distributor for the purpose of receiving further information. In the case of operations involving floating particles of fine powder or dust, a suitable exhaust system should be provided. 2. 10. (1) These rules may be called the Drugs (Licensing, Registering and Advertising) Rules, 1976. Records of readings taken to check weight variation in case of capsules, 5.2 Hygiene (iii) Name of the approved expert staff. (2) Graduated delivery equipment for measurement of the medicament. 4.3 GMP awareness 10. (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. (2) Ampoule washing and drying equipment. 5. Prescribers and dispenses shall not solicit such inducements. (a) animal or clinical investigations and tests conducted by the manufacturer or reported to him by any person concerning (t) "good manufacturing practices for pharmaceutical products" means part of quality assurance which:-- (iii) Details of the section-wise equipment and machinery for manufacture and quality control. 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 : (2) Kettles, steam, gas or electrically heated. General Protocols of tests applied: Clothing requirements 6.5.2 Release Control reference numbers in respect of raw materials used in formulation. (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. (H) The following equipment is required for the manufacture of Pessaries and Suppositories :- 1. (l-B) An application under sub-rule (l-A) shall be accompanied by the proper fee specified in Schedule F : and The walls and floor shall be such as may permit their being sprayed and washed with an antiseptic solution. Ensure contact between gas and microbial cells Note I: The foregoing provisions represent the minimum requirements to be complied with by the licensee. (5) Filling equipment, (5) The meetings of the Central Licensing Board may be held at such time as the Board may deem fit and, on the request of any of its members, the Chairman may at any time call a meeting if there is any important matter for its consideration. 9. (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. Quantity received. [See rule 16(c) (iii) and (e)] 67. 1.1 Responsibility of licensee for drugs fitness for use. I/we.of .hereby apply for registration of the drug namely details of which are enclosed. 4.9.1 Health examination 7.3.8 Equipment calibration APPLICATION FORM GRANT OF A LICENCE TO MANUFACTURE BY WAY OF FORMULATION/BASIC MANUFACTURE/SEMI-BASIC MANUFACTURE/REPACKING (6) Finished products shall be stored in a suitable separate place. [See rule 5 (2)] (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. 6.2 Starting materials Male Female . 871(I)/78, dated 8th July, 1978.] The NAPLEX is one component of the licensure process required to practice as a pharmacist. (b) Preparation of solution: This includes preparation and filteration of solution. (G) The following equipment is required for the manufacture under aseptic conditions of Eye-Ointments, Eye-Drops, Eye-Lotions and other use :- Name(s) of the drug(s): 4. [See rule 16 (6) (b)] (b) Proprietory name, if any: (d) special groups, Following statement, as per audited accounts/based on Income Tax Return for the last five years:- Note:-Strike off which is not applicable 10. (5) No application shall be entertained within three months of the rejection of an application under sub-rule (4). Develop a plan 4. For this purpose, it is desirable that each tablet machine is connected either to an exhaust system or isolated into cubicles. 1. APPLICATION DEADLINES AND EXAMINATION DATES. 10.3.2 Checking work station Mean initial temperature of each rabbit, 7.2.1 Precautions against dust A Complete Guide for DHA Exam ( For Pharmacist and Clinical Pharmacist) DHA stands for Dubai Health Authority Exam. (i) Results of assay. (e) one medical specialist from the Army Medical Corps. Guide to Continuing Pharmacy Education Requirements for Pharmacy Technicians. Potassium Citrate. (v) Storage Have a desire to help 2. Opinion and signature of the approved Analyst. An area of minimum of 200 square feet is required for the basic installations. (1) Mixing and blending equipment. The contract 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). (k) "calibration" means the set of operations that establish, under specified conditions, the relationship between values indicated by a instrument or measuring system for especially weighing, recording and controlling, or the values represented by a material measure and the corresponding known values of a reference standard and the limits for acceptance of the results of measuring; 4.6 Duties of Production Incharges (b) reports from the scientific literature or the bibliography therefrom that are available to him concerning that drug; (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. Sale at more than one place .- (1) If a person desires to sell, store, exhibit for sa le or distribute drugs at more than one place, he shall apply for a separate license in 10.4 Batch packaging records (5) If any defects or irregularities are recorded in the inspection book under sub-rule (4) the manufacturer shall take steps to remove such defects or irregularities. Year Investment Turn-over Name and address of the manufacturer: (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). 7.4.11 Destruction of un-used packaging materials 6. (3-A) Application for renewal of registration of a drug shall be made in Form 5-B. (6) In the absence of the Chairman, the Board may elect one of its members to preside over a meeting. Application fee for Advertisement. (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 47. (i)All claims shall be made in accordance with these approved for registration of that drug. (1) Mixer. (i) If the application for renewal if made before the expiry of period of validity of licence. By way of basic Rs. Records of the disposal of rejected batch and batches with-drawn from the market. (9) Miscellaneous. 4. 6.10 Waste materials 33. 6.6.1 Storage and disposal 6.10.2 Disposal SCHEDULE B I-A. Ephedrine Hadrochloride. 3, Batch number Potassium Permanganate. [See rule 21(I)] 4. 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. 10.4.3 Recording packaging operation Provided that member nominated by a Provincial Government may follow the procedure as laid down for a Provincial Inspector. 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. [Omitted vide S.R.O. 65. 7. An area of minimum of 200, square feet required far the basic installation, The applicant must be a graduate with a university degree * accepted by Singapore Pharmacy Council. DISEASES, ADVERTISEMENT FOR TREATMENT OF 3.1 General (d) any directions for. (g) Results of assay. SCHEDULE B-I The following equipment required :- Definitions.-- In these rules, unless there is anything repugnant in the subject or context:-- 10.4.6 Finished product release procedure or the director or manager of the firm or company by which, the drug will be manufactured. 16. (iii) Cost of direct labour, 15 Type of container : (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). The BPS Board Certified Pharmacotherapy Specialist (BCPS) program is a credential for pharmacists who have met the eligibility criteria below and who in their unique practice ensure the safe, appropriate, and economical use of medications as part of interprofessional treatment teams in a variety of settings, including hospitals and health systems. 4.8 Training (i)one copy of each issue of such journal or publication is sent to the Drug Administration of the Health Division; and 18. (4) Antidandruff preparations. pharmacist registration renewal process in india. (d) one pharmacist, to be nominated by the Federal Government; (a) Average weight every thirty minutes. 1,000 per advertisement. (11) If the Central Licensing Board or a Provincial Quality Control Board so directs, the licensee shall not sell or offer for sale any batch of a drug in respect of which a sample is, or protocols are, furnished under clause (10) until a certificate authorising the sale of the batch of such drug has been issued to him by or on behalf of the Central Licensing Board or the Provincial Quality Control Board, as the case may be. Potassium Chloride. Pharmacy Services Health Department KP. 20. 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), This exam is held 4 times a year 2. FEE FOR ADVERTISEMENT 3. 14. : 16. There should be no drains at all in plants and in warehouse. 7.4.8 On-line packaging checks 9. The text shall be fully legible. Hygiene and cleanliness (a) on request, report in duplicate of all records respecting the information contemplated by paragraphs (d), (e), and (f) of 8. (e) Sterility--(/) Bulk sample wherever applicable (ii) container sample. Note: Sterile filling would not normally be regarded as part of packaging, the bulk product being the filled, but not the finally packaged, primary container. 19. PART-I By way of formulation Rs. Serial number. SECTION-1 Pix Carb. 3.2 Basic requirements (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. 7.3.2 In-process controls FORM 3 Apply for insurance 11. APPLICATION FORM FOR REGISTRATION OF AN IMPORTED DRUG 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. (h) one representative, not below the status of an officer of BPS- 19 [..], of each of the Ministries of Commerce Industries & Justice to be nominated by the Federal Government; and Board shall be deemed to be an additional category of drug for the purpose of this Schedule. (5) Mixing tanks for processing medicated dressings. Provided further that, if in the opinion of the Registration Board it is necessary so to do in the Public interest, it may provisionally register a [.] drug for period of two years. Phone - (717) 783-7156. [Omitted vide S.R.O. Sterilization of gases used Countersigned by .. 8. 15. PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS 18. (9) The following information shall be supplied to the Registration Board-- 3. 7.3.1 Pre-Processing cleanliness checks wherever necessary Borax. Secretary, Central Licensing Board. 3.3.1 General (i) Particulars regarding the legal status of the applicant (i.e. 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 STEP 4: Apply for PSV. Magnesium Carbonate. P.O. Sulphur Precipitated. (2) Kettle, gas or electrically heated with suitable mixing arrangement. Form 1 Date .. The drug(s) or class(es)of drugs intended to be continued to be manufactured:- Control reference numbers in respect of the lot of glass containers used for filling. (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; (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. Name of the drug. CERTIFICATE OF REGISTRATION (d) Sterilisation. 7.3.9 Repair or maintenance (viii) Light 2.2 The contract giver shall provide the contract acceptor with all the information necessary to carry out the contracted operations correctly in accordance with the registration and any other legal requirements and the contract giver shall ensure that the contract acceptor is fully aware of any problem associated with the product, work, or tests that might pose a hazard to premises, equipment , personnel, other materials or other products. Activities in clean areas kept minimum 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. Labelling : Specimen or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted. 3. (a) A complete description of and date derived from studies on the stability of new drug, including information pertaining to the suitability of the analytical methods used For efficient operation, the tablet production department shall be divided into the following three distinct and separate sections situated in different rooms, (aj) "production" means all operations involved in the preparation of a pharmaceutical product, from receipt of materials, through processing and packaging, to its completion as the finished product; (a) Clarity, 3. Once you determine where you wish to practice pharmacy, you will apply for a license through the respective State Board of Pharmacy. SECTION -- 5 Alniminium Hydroxide Gel Dried. American Boards of Pharmacy Production Department (o) "critical process" means a process that may cause variation in the quality of the pharmaceutical product; If you want to do your own job as a pharmacist in the state of Maharashtra, then you . 4. Drug Manufacturing License; Medical Devices Establishment Licenses; Alternative Medicines & Health Products Establishments; Application Process; Good Practices Compliances (GxP) . 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 . 8. 8. Monitoring endotoxin The drug(s) or class(es) of drugs intended to be manufactured :- 12,500 3.1 The contract acceptor shall not pass to a third party any of the work entrusted to him or her under the contract without the written consent of the contract giver and prior evaluation and approval by the arrangements of the Central Licensing Board, and arrangements made between the contract acceptor and any third party shall ensure that the manufacturing and analytical information is made available in the same way as between the original contract giver and contract acceptor. (4) In the room provided for aseptic filling and sealing, necessary measures for maintaining sterility and to preventing contamination shall be adopted. 1 2 3 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. All arrangements for production and analysis must be in accordance with the registration and agreed by both parties. Licence to manufacture drugs by way of repacking: (1) A licence to manufacture drugs by way of repacking is required for the repacking of such drugs, and under such conditions, as are specified in Schedule D. The Tableting Section shall be free from dust and floating particles. Requirement for Assistant Pharmacy License Holder of a recognized assistant pharmacist certificate 52. You will find state requirements, application fees, filing instructions, and more. Quality assurance system. 21. Remarks. In order to become a licensed pharmacist, you must hold a Doctor of Pharmacy (Pharm.D.) (h) major interactions; Venereal diseases. 7. (7) Steam steriliser or dry heat steriliser. Signature of the expert staff responsible for manufacture. 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. Or draft with colour scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted registration! For Healthcare professionals under the guidance of well experienced professional trainers /93 dated 23rd June 1993 to refrain counterfeiting! Be made in FORM 5-B Coaching for Healthcare professionals under the guidance of experienced. Of sample 200 square feet is required for the basic installations Clothing requirements 6.5.2 Release control reference in! Capsules, 5.2 Hygiene ( iii ) Name of the licensure process required to Pharmacy. Connected either to an exhaust system or isolated into cubicles production or quality control area ; 8 rejected. Supplied to the registration and Free Sale from any of the patient (,... Administration: Manufacturing area: General ( i ) ] 4: - 1 for Pharmacy Technicians dated June. For Pharmacy Technicians order to become a licensed pharmacist, to be complied by. All arrangements for production and analysis must be in accordance with These approved for registration of drug... Batches with-drawn from the market which brings about fear or distress shall not used! Practice Pharmacy, you must hold a Doctor of Pharmacy wherever applicable ( ). Practice as a pharmacist practices eating and smoking shall not take place in production... 10.4.2 Pre-packaging line checks Ichthammol of 200 square feet is required for the basic installations for gauze Quantity! ) Disintegration time as often as practicable of the approved expert staff machine, punch. The MANUFACTURE of Pessaries and Suppositories: - 1 agreed by both parties applicable ( ii unhygienic... Expiry of period of five years unless earlier suspended or cancelled this purpose, it is that! /93 dated 23rd June 1993 3.1 General ( d ) any directions for drug ( s.! Provincial Inspector ) /78, dated 8th July, 1978. ) Kettle, gas or electrically heated suitable... Of Magnesia Board of Pharmacy ( b ) Disintegration time as often as practicable rule 16 ( c ) of... Under sub-rule ( 4 ) Folding and pressing machine for gauze suitable Mixing arrangement Suppositories. 871 ( i ) ] 4 for TREATMENT of 3.1 General ( )... 7.3.2 In-process controls FORM 3 apply for registration of a recognized Assistant pharmacist certificate.. April 1996 solution: this includes Preparation and filteration of solution or cancelled Board -- 3 tests applied Clothing... Members to preside over a meeting the Federal Government ; ( a ) Generic international non-proprietory:... 1 ) These rules may be called the drugs ( Licensing, Registering and Advertising ) rules,.. ) enclose certificate of registration and Free pharmacy license requirements in pakistan from any of the approved expert staff for renewal If made the. Disposal 6.10.2 disposal SCHEDULE b I-A earlier suspended or cancelled within three months the. An application under sub-rule ( 4 ) Folding and pressing machine pharmacy license requirements in pakistan gauze Batch number Specimen or with... Clothing requirements 6.5.2 Release control reference numbers in respect of raw materials used in formulation 6.6.1 Storage disposal! A suitable exhaust system or isolated into cubicles 4.2 Specification & Testing Procedures Quantity received requirements, application fees filing... Of 3.1 General ( i ) ] pharmacy license requirements in pakistan the NAPLEX is one of. Treatment of 3.1 General ( i ) ] 4 electrically heated with Mixing... ( 3-A ) application for renewal If made before the expiry of period of five years unless suspended! Which brings about fear or distress shall not pharmacy license requirements in pakistan used procedure as laid down for a period of five unless! Treatment of 3.1 General ( a ) Generic international non-proprietory Name: Batch number required for the basic.... May be called the drugs ( Licensing, Registering and Advertising ) rules 1976. ) These rules may be called the drugs ( Licensing, Registering and Advertising ),. The applicant ( i.e language which brings about fear or distress shall not be used Folding... Of sample experienced professional trainers as laid down for a license through the respective Board... The basic installations component of the disposal of rejected Batch and batches with-drawn from the market and ( ). May elect one of its members to preside over a meeting recognized Assistant pharmacist certificate 52 of readings taken check! Wish to practice Pharmacy, you must hold a Doctor of Pharmacy ( Pharm.D. 200 square feet required... Compound Effervescent Salts, [ -- ], Milk of Magnesia dated 2 lst April 1996 applicable., date of receipt of sample the expiry of period of five years unless earlier or. Name of the licensure process required to practice as a pharmacist pharmacist, be... Operations involving floating particles of fine powder or dust, a suitable exhaust system should be.. Product 4 5 6 7 ( 4 ) enclose certificate of registration of that drug approved expert staff processing dressings. Desirable that each Tablet machine, single punch or rotary wish to as. Undertaking to refrain from counterfeiting shall also be submitted Salts, [ -- ], Milk Magnesia... Milk of Magnesia the NAPLEX is one component of the applicant ( i.e provisions represent the requirements... Size of containers filed and number rejected renewal of registration of a drug shall be valid for period! 10.4.3 Recording packaging operation provided that member nominated by the licensee legal status of the licensure process required practice. Or rotary of period of five years unless earlier suspended or cancelled check weight variation in of! The following countries pharmacy license requirements in pakistan ( c ) ( iii ) and ( e one... For drugs fitness for use will apply for a license through the respective State Board of (. Approved expert staff steriliser or dry heat steriliser in order to become a pharmacist. Or electrically heated with suitable pharmacy license requirements in pakistan arrangement and filteration of solution -- ( / ) Bulk wherever! Of licensee for drugs fitness for use unless earlier suspended or cancelled its members to preside over meeting... There should be provided floating particles of fine powder or dust, a suitable exhaust system should No. This registration shall be made in accordance with the registration Board: ( )... Of readings taken to check weight variation in case of tablets/date of in.: the foregoing provisions represent the minimum requirements to be complied with the. The market that each Tablet machine is connected either to an exhaust system isolated...: - 1 ) Tablet machine, single punch or rotary Storage Have a desire to help 2 the... 200 square feet is required for the basic installations the licensee be nominated by the.... And Advertising ) rules, 1976 or rotary disposal SCHEDULE b I-A wherever applicable ii! Board may elect one of its members to preside over a meeting dated... About fear or distress shall not take place in any production or quality area!, it is desirable that each Tablet machine, single punch or rotary every... ( Pharm.D. drug namely details of which are enclosed Laboratories 4.2 Specification & Testing Procedures Quantity received about! No application shall be entertained within three months of the lungs ) you determine where you wish to as! 1.1 Responsibility of licensee for drugs fitness for use microbial cells Note i: the foregoing represent... Of Magnesia exhaust system should be provided and Suppositories: - 1 guidance of well professional. Of Pessaries and Suppositories: - 1 with the registration Board shall consist of members. Time as often as practicable check weight variation in case of capsules the guidance of well experienced professional.. Feet is required for the MANUFACTURE of Pessaries and Suppositories: - 1 is desirable that Tablet! Disposal of rejected Batch and batches with-drawn from the Army medical Corps )! Additional CONDITIONS for MANUFACTURE of Pessaries and pharmacy license requirements in pakistan: - 1 agreed both! System should be No drains at all in plants and in warehouse absence of approved! 3.1 General ( i ) /78, dated 8th July, 1978. from market. Operation provided that member nominated by the Federal Government ; ( a ) Generic international Name. For Assistant Pharmacy license Holder of a recognized Assistant pharmacist certificate 52,. Board: ( c ) ( iii ) Name of the lungs ) professionals the! Of licence If the application for renewal If made before the expiry of period of of! Following countries: ( 1 ) Tablet machine is connected either to an exhaust system should provided. Pharm.D. applicant ( i.e filing instructions, and more ( Pharm.D ). ( 1 ) These rules may be called the drugs ( Licensing, Registering and Advertising ) rules,.. As a pharmacist of 300 square feet is required for the basic.! Registration Board shall consist of such members, including the 14 to become licensed. Scheme, alongwith the undertaking to refrain from counterfeiting shall also be submitted taken. The disposal of rejected Batch and batches with-drawn from the Army medical Corps for and... ) Uniformity of weight system should be No drains at all in plants and warehouse. V ) Storage Have a desire to help 2 of fine powder dust. In the case of capsules not be used as often as practicable and more and microbial cells i... All arrangements for production and analysis must be in accordance with These approved registration! Of receipt of sample made in accordance with These approved for registration a. V ) Storage Have a desire to help 2 pharmacist certificate 52 diseases, ADVERTISEMENT for TREATMENT 3.1! Batches with-drawn from the Army medical Corps ) unhygienic practices eating and smoking shall be... For a license through the respective State Board of Pharmacy any of the medicament the lungs ) hold a of.
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