Vaccines for the Prevention of Viral Hepatitis B for patients on Chronic Dialysis Treatment

Дополнителни информации

The economic operators should meet the following conditions:

Based on the previously received written request on behalf of the authorized person of each centre separately, the offered goods must be delivered to the following locations, based on the technical specifications:

— PHI Center for Public Health — Skopje, located at nr.18„ 3rd Macedonian brigade“ str., Skopje

— PHI Center for Public Health — Veles located at nr.14„ Lazo Osmakov“ str. Veles,

— PHI Center for Public Health — Kumanovo located at n.n„ 11th October“ str, Kumanovo,

— PHI Center for Public Health — Tetovo located at nr.73„ 29th November“ str., Tetovo,

— PHI Center for Public Health — Prilep located at n.n„ October“ str.. Prilep,

— PHI Center for Public Health — Kochani located at nr.21„ Milan Zaechar“ str. Kochani,

— PHI Center for Public Health — Bitola located at ул.n.n„ Partizanska“ str. Bitola,

— PHI Center for Public Health — Strumica located at n.n„ Panche Peshev“ str.. Strumica and

— PHI Center for Public Health — Ohrid located at n.n„ Sirma Vojvoda’ str. Ohrid.

After the delivery of the public procurement contract is done, the invoices should be submitted in the archives of each centre, in accordance with the contract for public procurement, with a deferred payment of at least 90 days.

— Upon reception of the subject of procurement, the shelf life should not be shorter than 1 year from the overall duration of the subject of procurement, except for item 10 (code 8112 — Influenza vaccine) vaccine against seasonal influenza,

— to maintain/meet the shelf life of item 10 (code 8112 — Influenza vaccine), the deadline of which should be in accordance with the recommendations of the WHO, but not longer than 1 year,

— the subject of procurement is to be on the WHO List of Pre-qualified Vaccines, with the exception of items 3 (Hepatitis A, inactivated, whole virus) and item 10 (code 8112 — Influenza vaccine) which should be approved for use and be located in the EU Member States, Norway, Switzerland, USA, Canada and Japan,

— The procurement subject — vaccines should possess a certificate for releasing a batch of the drug on the market (OCABR — Official control authority batch release certificate), or equivalent, in accordance with the recommendations of the EU, not older than 3 years, except for item 7 (code 8108 — Pneumococcus, purified polysaccharides antigen conjugated) of the technical specifications.

The contractor of the procurement has to submit the following documents for proving the fulfillment of the above mentioned conditions:

— a declaration that the overall alloted time of the procurement subject on the date of delivery should not be shorter than 1 year from the overall duration of the subject of procurement except for item 10 (code 8112 - Influenza vaccine),

— a statement signed and certified by the economic operator that the shelf life for item 10 (code 8112 — Influenza vaccine) will be in accordance with the recommendations of the WHO, but not longer than 1 year,

— to submit the list of pre-qualified WHO vaccines with the exception of item 3 (Hepatitis A, inactivated, whole virus) and item 10 (code 8112 — Influenza vaccine), for which a certificate for a pharmaceutical product, issued by a competent administrative body, not older than 3 years (CPR), should be submitted as an evidence that it is approved for use and is on the market in an EU Member state, Norway, Switzerland, USA, Canada and Japan,

— to submit a certificate for releasing a batch of the drug on the market (OCABR — Official control authority batch release certificate), or equivalent, in accordance with the recommendations of the EU, not older than 3 years, except for item 7 (code 8108 — Pneumococcus, purified polysaccharides antigen conjugated) of the technical specifications.

Информации за овластени лица и постапка за отворање

Authorized representatives of the economic operators of public opening must have an authorization signed by the authorized person of the economic operators at the public opening of tenders may attend any interested person. Only authorized representatives of the bidders may participate in the proceedings of a public bid opening by giving their comments in the minutes of the bid opening.