Decree of the Ministry of Health and Social Affairs of the Czech Socialist Republic, Federal Ministry of National Defence, Federal Ministry of Interior, Federal Ministry of Transport, Ministry of Interior of the Czech Socialist Republic, Ministry of Justice of the Czech Socialist Republic and Ministry of Agriculture and Nutrition of the Czech Socialist Republic No. 61 / 1990 Coll.
Decree of the Ministry of Health and Social Affairs of the Czech Socialist Republic, the Federal Ministry of National Defence, the Federal Ministry of Interior, the Federal Ministry of Transport, the Ministry of Interior of the Czech Socialist Republic, the Ministry of Justice of the Czech Socialist Republic and the Ministry of Agriculture and Nutrition of the Czech Socialist Republic on the management of medicines and resources
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Effective from 01.04.1990
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61
DECLARATION
Ministry of Health and Social Affairs of the Czech Socialist Republic, Federal Ministry of National Defence, Federal Ministry of Interior, Federal Ministry of Transport, Ministry of Interior of the Czech Socialist Republic, Ministry of Justice of the Czech Socialist Republic and Ministry of Agriculture and Nutrition of the Czech Socialist Republic
of 20 February 1990
on the management of medicines and resources
The Ministry of Health and Social Affairs of the Czech Socialist Republic, the Federal Ministry of National Defence, the Federal Ministry of Interior, the Federal Ministry of Transport, the Ministry of Interior of the Czech Socialist Republic, the Ministry of Justice of the Czech Socialist Republic, the Ministry of Agriculture and Nutrition of the Czech Socialist Republic, in agreement with the other participating authorities, provides, pursuant to § 70 (1) (c), § 79 (4) and § 80 (1), (4) and (5) of Act No. 20 / 1966 Coll., on the care of the health of the people, taking into account § 72 of the Ministry of Health Decree No. 42 / 1966 Coll., on the provision of medical preventive care:
Prescription procedure
Prescription of medicinal products for human use (hereinafter referred to as "medicines') and medical devices (hereinafter referred to as" devices') in accordance with a special Regulation (17) for the account of the relevant health insurance undertaking (hereinafter referred to as "insurance undertaking ') 18) or for the insurance and sickness insurance undertaking or for the account of the patient shall be entitled:
(a) doctors providing first aid for the insurance undertaking's account;
(b) doctors providing health care
1. in medical establishments for the account of an insurance undertaking or an insurance undertaking and a sick or sick person;
2. in social care facilities for the account of the Insurance Company, both for receptional forms and for applications.
(1) Physicians prescribe, on the basis of an examination of a sick drug that is included in a pharmacopoeia or the use of which is authorised by the Ministry of Health of the Czech Republic (hereinafter referred to as "the Ministry"). When prescribing medicines and devices, they are required to act effectively and when prescribing medicines and funds to the account of the Insurance Company in accordance with the principles set out in a separate regulation. 19)
(2) Prescription of medicines and devices including the number of packs and dosage must be recorded in the patient's medical documentation. Medicines are prescribed for patients on the receptor form; 20) if medicines containing group I narcotic substances are listed (21) and group II psychotropic substances (22) are prescribed for patients on a specific receptor form. 23) The funds are prescribed for the patient for the medical and orthopaedic form. 24)
(3) Physicians may prescribe medicines which are necessary for the performance of diagnostic, preventive and therapeutic activities as provided for in their workload and whose indications and effects they are familiar with. The funds paid in full by the Insurance Company can only be prescribed by doctors in a version that the insured persons fully meet and satisfy the conditions of the least economic difficulty.
(4) When providing first aid, only medicines necessary for the provision of such assistance and in the amount needed until the time of the visit to the doctor.
(5) A maximum of two types of mass-produced medicinal products may be prescribed for one receptor form, except as provided in Section 13 (3), or only one type of medicinal product produced individually. If only one type of medicine is prescribed, the prescriber must cross the remaining empty space.
(6) When prescribing multiple original drug packages or multiple doses individually (magistraliter), the prescribing physician shall indicate the number of packages or doses in Roman numerals and in words.
(7) Physician completed
(a) the recipe form (hereinafter referred to as "the recipe"),
(b) the form of the voucher for the medical and orthopaedic aid (hereinafter referred to as the voucher) shall be accompanied by the following particulars:
1. name, surname, birth number, address of the sick person;
2. the prescription of the medicinal product; the intended excess of the highest dose of the medicine must be marked with the symbol ("!") and written in words. If the doctor insists on the prescribed medicine or device, he shall mark it with the symbol "R ';
3. only pharmaceutical names and abbreviations may be used when prescribing individually prepared medicines, for mass-produced medicines of their registered names (trade marks); when prescribing medicinal products with an international non-generic (generic) name, the physician is required to refer to the active substance concentration recipe;
4. instructions for use of the medicinal product (device);
5. the signature of the prescriber and the date of issue of the prescription (voucher);
6. the stamp of the medical establishment bearing the stamp of the prescribing doctor; for first aid doctors, only a stamp with his nametag and address.
(8) Recipes (vouchers) containing prescribed medicinal products (devices)
(a) marked with the letter "Z" in the list of medicinal products and medical devices annexed to the specific Regulation, 19)
(b) in excess of the maximum fixed remuneration, the insurance undertaking shall have the particulars referred to in the preceding paragraph and shall bear the stamp of the competent medical examiner, his signature and the date on which he did so.
(9) If a prescriber prescribes a drug or a device in which he is involved in payment under a special regulation (19), he shall notify the patient accordingly.
Prescription and ordering of medicines for medical devices
(1) For medical devices, medicines are ordered for requests25) (order forms); medicines containing group I narcotic substances and group II psychotropic substances are ordered for requests22). 26) Medicines can also be ordered by computer.
(2) The documents referred to in paragraph 1 shall bear the stamp of the department, the namesake and the signature of the prescribing doctor and shall be signed by the head of the department or his representative.
Method of prescribing medicines for the patient
(1) Medicinal products are prescribed on the account of the patient if the citizen expressly so requests.
(2) Medicinal products and devices for the account of the patient are prescribed in accordance with the principles set out in Sections 1 and 2.
(3) Prescribers shall indicate on the prescription how many times the dispensing of the medicine may be repeated, but for a maximum period of 1 year from the date of issue of the prescription. Without this information, the recipe has the same period of validity as the recipe on behalf of the state health administration. The doctor must not mark the repeat dose on the prescription for narcotic drugs and psychotropic substances or drugs at an increased risk of drug addiction. The handling fee shall not be levied in this case.
Reception forms and duration of recipes
(1) The medicinal products are prescribed on the prescription forms issued by the medical establishment in or for which they work, or in the district of which they are resident, to doctors and with stamps.
(2) Physicians are required to ensure the deposit of receptor forms and stamps in order to prevent their alienation and the possibility of their misuse or falsification. The loss of an empty recipe form or a request form shall be reported to the head of the relevant medical institution without delay to the competent department of the Police Department of the Czech Republic and to the medical report of the District Office.
(3) Special stamps are used when prescribing medicines in the first-aid medical service.
(4) The recipe has a limited duration. The recipe for group I narcotic substances (2) and psychotropic substances (3) expires 5 days after exposure to antibiotics and antimicrobial chemotherapeutic agents. The recipe for other medicines is valid, unless otherwise specified by the prescribing physician, for 1 week from the day of exposure. The recipe issued during the first aid medical service is valid for the following day at the latest.
Procedure for dispensing medicines
(1) Medicinal products.6) In places where there is no pharmacy, the dispensation of veterinary medicines and veterinary equipment is provided by the auxiliary equipment set up by the veterinarian, who issues medicinal products from the basic stock for payment. The veterinarian shall take the basic supply from the pharmacy.
(2) Some medicines may be given to patients without a prescription. The list of these medicines is set out in the Annex to this Decree.
(3) A fee is usually levied at the pharmacy when dispensing medicines prescribed for the prescription. 7)
(4) If the prescription prescribing physician does not indicate the package size, the smallest packaging included in the list of medicinal products and medical devices annexed to the specific regulation shall be issued. 19) Similarly, unless the concentration of the medicinal product intended for a particular age group is indicated, action shall be taken.
(5) If the prescription lacks the required requirements and cannot be verified for serious reasons, medicinal products should not be issued.
(6) If two types of medicines and devices are prescribed on the recipe and if one of them is not available and cannot be readily procured, the pharmacist shall issue a prescription extract (voucher) bearing the name "Extract 'on the missing medicine or device. The extract must contain all the original recipe (voucher). The original recipe (voucher) shall bear the note" Extract received. "The provisions on the duration of the prescription (voucher) shall apply to the extract and shall be calculated from the date of the extract.
(7) If prescribed medicinal products are not available at the pharmacy, they shall be replaced by another pharmacist, which shall be the same as the content or concentration of the active substances. If the drug differs in the content or concentration of the active substances, the pharmacist, after consulting the prescriber, shall adjust the dosage to the extent prescribed. Exceptionally, the missing drug may be replaced in accordance with the contents of the sentence, first and second, by another medicine, the reimbursement of which is more financially costly for the sick. The pharmacist will alert the patient to the change of medicine and mark it on the recipe. If the prescribed pack size differs from that of the original package, the pharmacy shall issue the nearest package corresponding to the recipe and the pharmacist shall indicate this on it.
(8) Individually prepared medicinal products that have not been collected at the time of the hospital are only kept in the pharmacy for the duration of the prescription (extract). This is indicated by the pharmacist on the recipe (extract).
(9) The lead pharmacist shall inform the local district insurance company of the situation in the supply of the medicinal products.
(10) The recipe (voucher) for which the medicinal product has been issued, the pharmacy shall bear its stamp, an indication of the price of the medicinal product issued and the date of its issue.
Medicinal products for medical devices
(1) Narcotic substances and psychotropic substances may be issued no later than 5 days after the date of issue of the order.
(2) At the time of issuing the ordered medicines and the means, they must confirm their receipt on the original and the receipt of the request by signature by the authorised staff of the department of the medical institution. Narcotic substances and psychotropic substances may be taken over by a doctor or an authorised central healthcare professional.
Medicinal products to other customers
(1) The collectors referred to in Sections 25 to 31 may be given medicines and special order products in pharmacies. Where medicinal products subject to medical prescription are required, the special order must be signed by the doctor and stamped with a medical device. Products subject to the veterinary prescription may also be issued to an order from a breeding organisation certified by the competent veterinarian, provided that the order contains the particulars specified in the specific regulation. 15)
(2) Narcotic substances and psychotropic substances must not be supplied to these customers unless they are authorised to handle them. 8)
Samples of foreign pharmaceuticals for clinical trials
(1) Samples of foreign pharmaceuticals which are not registered in the Czech and Slovak Federal Republic and are intended for clinical evaluation or research and which are sent in quantities of more than 5 packages to the address of the medical institution or the doctor working there may receive, take over and use them for the purpose only after prior approval by the Ministry.
(2) The samples of foreign pharmaceuticals that have been taken over by the Ministry of Health at the authorisation of the Ministry of Health shall be administered by that establishment as well as by other medicines.
(3) The samples of foreign pharmaceuticals for the purpose of the registration procedure are provided by the Ministry of Organisation designated by it.
Treatment of narcotic substances and psychotropic substances and drugs at increased risk of drug addiction
Prescription of drugs containing narcotic substances and psychotropic substances and drugs at increased risk of drug addiction
(1) Products containing narcotic substances, psychotropic substances and those at increased risk of drug addiction9) are prescribed either for special receptor forms (§ 2 (2)) and for special order forms (§ 4) or for standard receptor forms.
(2) Common receptor formsare prescribed for group II of the list, (2) psychotropic substances of Group III and IV of the List (3) and other drugs with an increased risk of drug addiction9) both monocomponent and combined.
(3) For patients in outpatient care, only one type of drug containing the drug group may be prescribed per receptor form I or group II psychotropic substances or drugs with an increased risk of drug addiction.
(4) When prescribing for a special receptor form (with a blue stripe), the prescribing physician shall complete the original and two copies of the form. The original and the first copy shall be given to the patient for the collection of the medicinal product at the pharmacy and the second shall be left in the block. When prescribing, the type, concentration (strength) of the medicinal product, the package size and the complete instructions for its use must be clearly and accurately indicated. When prescribing an individually prepared drug, the number of doses must be given by Roman numerator and word (e.g. D.t.d.). No X / decem /).
(5) For medical devices, the specific forms of applications (with a blue stripe) are prescribed for group I list 2) and group II psychotropic substances. The prescribing physician shall complete the original and three signatures. The original and two signatures shall be sent to the pharmacy, leaving the third copy in the block.
(6) The Directorate of Health keeps stocks of these special forms and their issue in strict records. It shall be issued to doctors in blocks by a staff member authorised by the Director in writing. The title of this form shall bear the name of the establishment by means of printing or stamp.
(7) Recipes or requests should be stored by your doctor to avoid alienation. Empty forms (recipes, vouchers) are not permitted to be stamped in advance with the stamp of the device and the name of the doctor. The loss of unused form or request must be reported immediately by the head of the establishment to the competent district office, authorities of the Czech Police and Ministry.
(8) Unused blocks of recipes or requests are returned to the facility's headquarters. Likewise, blocks (with signatures) are returned after using the last recipe or request. The Directorate shall keep these blocks for five years from the date of issue of the last regulation or request.
Preparation, supply and storage of narcotic drugs, psychotropic substances, drugs containing narcotic substances, medicines containing psychotropic substances and medicines at increased risk of dependence on drugs
(1) Narcotic substances, psychotropic substances, medicinal products containing narcotic substances and medicinal products containing psychotropic substances ("addicts"), and medicinal products with an increased risk of dependence on them (27) may only be taken over, prepared, stored and issued in pharmacies.
(2) It is not permitted to prepare in pharmacies drugs containing group I narcotic substances (21) or psychotropic substances listed in group II (22), with the exception of medicines that cannot be provided by a supplier.
(3) Medicines containing narcotic substances listed in Group I of the List, 21) psychotropic substances listed in Group II of the List (22) and medicinal products at increased risk of dependence on them (27) may only be issued for recipes or requisites exhibited by:
(a) doctors providing health care under the provisions of Section 1;
(b) veterinary surgeons providing veterinary care.
(4) If a pharmacist finds out or suspects the prescription has been forged, he will not issue the medicine and is obliged to report such a case without delay to the authorities of the Czech Police.
(5) The destruction of defective or unfit addictive substances and medicinal products with an increased risk of dependence on them (27) is carried out by the lead pharmacist in the presence of a person designated for this purpose by the competent county authority. The lead pharmacist shall draw up a protocol on the destruction of those medicinal products, which shall include details of the time, place, quantity of specific medicinal products and the reason for their destruction. The protocol shall be signed by the lead pharmacist and the person in whose presence the medicinal products have been destroyed; the lead pharmacist is obliged to keep the protocol in the pharmacy for five years. For medical facilities under the jurisdiction of the Ministry of Justice of the Czech Republic, the Ministry of Agriculture of the Czech Republic, the Ministry of Interior of the Czech Republic, the Federal Ministry of Defence, the Federal Ministry of Interior and the Federal Ministry of Transport, the pharmacist responsible for this activity is responsible for the relevant department regulations.
(6) Medicinal products containing group I list substances, 21) codeine, ethyl morphine and mono-component medicinal products, such substances containing and containing psychotropic substances of group II lists (22) and ephedrine must be stored in pharmacies in metal lockable boxes, separate from other medicinal products.
Procedure for the provision of pharmaceuticals and the equipping of first-aid pharmaceuticals for bulk events and for the provision of medicines to citizens when travelling abroad
(1) In physical or sporting events, the medical devices and devices chosen by the organizer shall be provided by the medical practitioner who is obliged to pay the medicines and devices provided to the healthcare establishment.
(2) Mountain Services rescue stations provide medical devices and medical devices designated by the competent district authorities in whose districts the mountain services are located. These health establishments also provide for the reimbursement of these medicines and devices. Their equipment shall be agreed by the head of the Mountain Service with the head of the designated medical establishment, as specified by the relevant Mountain Service station.
(4) Spotorovci in the care of the Institute of Sport Medicine for Top Sport provides medicines when travelling abroad.
The provisions on the provision of medical services to Czechoslovak citizens when travelling abroad, in particular on the reimbursement of medicines bought for patients when staying abroad, apply to the provision of medical services to Czechoslovak citizens when travelling and staying abroad. 10)
Provision of appropriations
(1) The funds are prescribed by doctors providing medical care in accordance with the provisions of Section 1 in accordance with Part 2 of the list of medicinal products and medical devices annexed to the Special Regulation (19).
(a) patients with vouchers, 24)
(b) medical devices for applications.
Only one type of means can be prescribed for one voucher (24).
(2) Notes 24) must contain the particulars referred to in § 2 (7), the means must be clearly marked. For borrowed funds, the period of their intended use shall be indicated. The voucher shall be signed under the heading "Approved 'by the treating physician, unless the approval is reserved for the head of the department of the health care establishment or for the medical examiner of the insurance undertaking or, where appropriate, for his authorised physician.
(3) Unless otherwise specified by the physician, the voucher is for one month. The device shall be withdrawn within a month of the date on which its manufacture or issue has been determined. An extract may be issued from the voucher in a similar manner to that of the recipe; for the extract, the voucher form shall be used for the medical and orthopaedic aid. 24)
(4) The patient is obliged to treat the device properly; in the event of intentional damage, destruction or loss of the device he is obliged to pay the medical institution the damage caused.
(5) The device may be prescribed after the period of use specified in the list of medicinal products and medical devices annexed to the specific Regulation; 19) Insurance undertakings may change the useful time of the device. Carriages and lifting cars for immobile persons can be re-prescribed only on the basis of a disabling protocol issued by the relevant service organisation.
Provision of medical and orthopaedic prosthetics equipment for the public health administration
For disabled railway workers are prescribed to the account of Insurance
(a) therapeutic and orthopaedic prosthetics;
(b) other means only as part of the necessary health care which cannot be provided to them by railway health institutions.
Prescription and delivery of funds for the sick
If a person expressly wishes to purchase a device at his own expense, the prescriber shall mark the voucher with the note "Castle sick."
Records of appropriations
(1) Medical facilities report in the medical documentation of the patient
(a) glasses of all kinds, including the replacement of more expensive frames and glasses, contact lenses, sliding loops for reading, occlusion and binoculars; the documentation is kept by the expert eye doctor who carried out the examination or treatment;
(b) prosthesis, epitosis and orthopaedic footwear; the documentation is kept by the competent prosthetic physician,
(c) other means, with the exception of carriages and hoists for immobile persons and hearing aids; the documentation shall be kept by the relevant departments.
(2) Medical establishments register on listing28)
(a) means, with the exception of carriages and hoists for immobile persons and hearing aids, in each of the relevant departments;
(b) carriages and hoists for immobile persons and baby carriages for disabled children in the relevant professional departments;
(c) hearing aids in the phonographic departments.
(3) Health care establishments shall carry out the inventory of the devices referred to in paragraph 2 on 31 December.
Funding
(1) Serum-manufactured and individually manufactured medical and orthopaedic prosthetics are covered by a medical device which has been provided by the device or for which a voucher has been prescribed under a special Regulation (19).
(2) Paragraphs 21 and 29 (4) are without prejudice to the provisions of paragraph 1.
Armed forces
Military services, institutes and facilities of the Czechoslovak army can collect both domestic and imported medicines and some resources from pharmacies
(a) for individual use in the reception forms for sickness care in the armed forces - warehouse. NV 118 / Z and NV 119 / Z,
(b) for the use of the infirmary in bulk on the SEVT form. No 14 284 0.
(1) Prescription of medicines and funds for medical care in the armed forces of the Czechoslovak army is governed by the Czechoslovak army regulations. 14)
(2) The requirements of the recipe and voucher are laid down in Paragraph 2 (7). The stamp shall contain the number (s) and place of the service or the stamp of the crew administration shall be used, marked "First-aid Crew."
(3) For the purpose of treatment facilities of military services, pharmacies designated by the head pharmacist of the medical establishment shall issue medicines in agreement with the head of the medical service of the department.
(4) Group I narcotic substances (2) and group II psychotropic substances (3) are prescribed for the warehouse recipe form. No NV 119 / Z where the name of the sick person is indicated "For the infirmary." In these cases, a separate delivery note is displayed at the pharmacy.
(5) Orders for medicines and devices must be signed by the head of the health service of the department.
(6) A fee is not levied for the supply of pharmaceutical orders from the Federal Ministry of Defence and its reception29) marked "For the infirmary."
Department of Correctional Education of the Czech Republic
(1) Prescription of medicines and devices in the Czech Correctional Education Corps is governed by the provisions of this Order and by the regulations of the Ministry of Justice of the Czech Republic.
(2) The Executive Services of the Medical Services of the Czech Correctional Education Corps, with the exception of medical institutions with their own pharmacy, receive domestic and imported foreign medicines and certain resources from pharmacies, namely:
(a) for individual use
1. on the receptive form 20) with a preprinted "SNV,"
2. Drugs containing group I narcotic substances (21) and medicines containing group II psychotropic substances (22) on a separate receptor form, 23)
b) in bulk for the need of executive facilities Medical services of the Czech Correctional Education Corps
1. on requests,
2. Drugs containing group I narcotic substances (21) and psychotropic substances (22) on the form. 26)
(3) Receptural forms (20) with pre-print "SNV" and special receptor forms (23) are recorded and provided by the central administration of the Medical Service of the Czech Correctional Education Corps. Other necessary forms, including forms for medical and orthopaedic aid (24), are provided by the medical services' executive facilities separately.
(1) Prescription of medicines and funds for the account of the Czech Correctional Education Corps shall be carried out according to the provisions of § 1 (1) (b) and (c) and § 2.
(2) The formula and the voucher of the funds must have the particulars provided for in Paragraph 2 (7) only:
(a) the address of the patient shall be indicated:
1. abbreviation "MS," if it is a member of the Czech Correctional Education Corps or a member of his family,
2. the stamp of the correctional institution or prison, if any,
(b) the identity card number, if applicable, is attached to the prescription of products containing group I of the list; (2) psychotropic substances of group II of the list (3) or those from an increased risk of drug addiction9) for a member of the family of a member of the Correctional Education Corps.
Police of the Czech Republic
(1) Prescription of medicines and devices in the Police of the Czech Republic is governed by the provisions of this Order with derogations for the Police of the Czech Republic. The authorities of the health services of the Czech Police are responsible for checking the accuracy and legitimacy of their prescription.
(2) Executive Medical Devices The Police of the Czech Republic and the Federal Police Force, with the exception of medical devices with their own constitutional pharmacy, collect domestic and foreign medicines and some of the resources from pharmacies
(a) for individual use
1. on the receptor forms marked "M,"
2. Products containing group I narcotic substances (2) and group II psychotropic substances (3) in the SEVT warehouse receptor form. No 26 283 0,
b) for the need of executive medical facilities Police of the Czech Republic in bulk
1. on request
2. Products containing group I narcotic substances (2) and group II psychotropic substances (3) on the SEVT warehouse form. No 26 285 0.
(3) The recipe and voucher of funds must have the same requirements as in the public health administration, only:
(a) instead of the address of the patient, the abbreviation "MV," if it is a member of the Police of the Czech Republic or a member of his family,
(b) the number of the identity card shall be added, if it is about the prescription of products containing group I of the list, (2) psychotropic substances of group II of the List (3) or those with an increased risk of drug addiction9) for a member of the family of a member of the Police of the Czech Republic.
(4) For sick persons in the field of the Ministry of Interior of the Czech Republic and the Federal Ministry of Interior of the Czech Republic outpatient care is prescribed for the account of the Insurance Company.
Veterinary care
(1) The recipes drawn up in the framework of veterinary care must have the formalities laid down in a specific regulation; 15) if these prescriptions are missing and cannot be verified for serious reasons, medicines should not be issued.
(2) In the cases indicated, a veterinarian may prescribe human medicines for use in veterinary care.
(1) Medicines and funds for the account of legal and natural persons (30) are issued for orders of medicines, (25) exceptionally for special orders signed by an authorised person. The substances listed in Group I of the List, 21) medicines containing group I of the List, 21) psychotropic substances listed in Group II of the List (22) and medicines containing psychotropic substances listed in Group II of the List (22) for legal and physical persons (30) shall be issued upon presentation of a recipe. 26) The prescribed records shall be kept on the consumption of narcotic drugs and psychotropic substances. Veterinarians prescribe products containing group I narcotic substances (2) and group II psychotropic substances (3) on a separate receptor form.
(2) If the recipe does not state "On behalf of a State Veterinary Service Organisation," medicines and funds shall be issued to the keeper of the animal.
(3) The prescription fee prescribed by the veterinarian is not levied.
(4) Medicinal products for the veterinary care of the armed forces and of the security corps are issued in individual cases for the recipes of the veterinary care of the armed forces, 31) for the need for military veterinary care organisations for applications used by medical devices, 25) Narcotic substances and drugs containing narcotic substances are prescribed on a separate form. 32)
Medicinal products and devices at individual wards of hospitals or other healthcare facilities, where appropriate, 33) shall be kept in the amount specified by the Director of the Health Facility.
(1) Medicines and devices must be stored clearly in accordance with the relevant legislation16) and must be treated economically. The head of the department responsible and the head nurse shall be responsible for the proper storage of medicines and resources.
(2) A group worker (a controlling pharmacist, a head of department, a head nurse and a representative of the economic and technical service of the establishment) shall dispose of non-compliant medicines and devices after prior approval by the Director, who shall also decide whether to prescribe compensation or other measures.
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Regulation Information
| Citation | Decree of the Ministry of Health and Social Affairs of the Czech Socialist Republic, the Federal Ministry of National Defence, the Federal Ministry of Interior, the Federal Ministry of Transport, the Ministry of Interior of the Czech Socialist Republic, the Ministry of Justice of the Czech Socialist Republic and the Ministry of Agriculture and Nutrition of the Czech Socialist Republic No. 61 / 1990 Coll., on the management of medicines and resources |
|---|---|
| Regulation Type | - |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 13.03.1990 |
|---|---|
| Effective from | 01.04.1990 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
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