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Nordmazedonien-Skopje: Medizinische Ausrüstungen, Arzneimittel und Körperpflegeprodukte
Abschnitt I: Öffentlicher Auftraggeber
Abschnitt II: Gegenstand
Specific Hematology Therapy for PHI UC for Hematology Skopje for a Period of 1 Year
Specific hematology therapy for PHI UC for hematology Skopje for a period of 1 year.
Specific hematology therapy for PHI UC for hematology Skopje for a period of one year
Abschnitt III: Rechtliche, wirtschaftliche, finanzielle und technische Angaben
Confirmation issued from authorized body for compliance of special criteria for performing legal business activity related to the public procurement subject. A decision issued by the Agency for drugs and medical aids of RM, approving whole sale trading with drugs.
List of employees responsible for the procurement phase, enclosing M1/M2 formulary for:
— declare a statement for engaged 24 hours available person for monitoring of the cold chain functioning and signalization in case of variations in the temperature range,
— declare a statement for full time employee with university degree in medicine or pharmacy in charge for pharmacovigilance and detection of problems in the drugs quality or errors in the drug’s series, submitting his/her data: name, surname, profession and contact phone in order to be available at any time,
— graduated pharmacist licensed to work in the procurement phases (reception, keeping and issuing drugs),
— submit notice for the parts of the procurement contract which the economic operator intends to transfer to subcontractor.
— declare a statement that the conditions for drugs safe keeping, accommodation, transport and managing are fulfilled pursuant to the Guidance for the conditions related to the space, equipment and human resources for awarding approval for whole sale trade with drugs (Off. Gazette of RM No 151/08),
— declare a statement that at the moment of reception of the drugs, the expiry date shall be at least 12 months valid out of the total drugs expiry date,
— if the drug does not have trade approval in RM, then approval for trading in EU members, Norway, Switzerland, USA, Canada and Japan,
— Pharmaceutical Quality Assurance Certificate issued by the manufacturer not older then 3 years or CPP certificate issued by the manufacturer not older then 3 years,
— decision for trading with medicines in Macedonia or temporary approval for parallel import or final approval for parallel import pursuant to the Law on drugs and medical aids in RM.
Abschnitt IV: Verfahren
Abschnitt VI: Weitere Angaben