Vvkt.lrv.lt

Health technology assessment

WEBSubmitted applications information (in Lithuanian): Download Health Technology Assessment – what is it? Health technology assessment (HTA) refers to the systematic …

Actived: 2 days ago

URL: https://vvkt.lrv.lt/en/health-technology-assessment/

Authorisation procedures

WEBTo transfer Marketing Authorisation during the procedure, the original of the transfer agreement signed by both sides should be submitted to [email protected] and a hard …

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Information to the applicants

WEBThe Order No. 159 of the Minister of Health of the Republic of Lithuania of 5th April 2002 ““Regarding approval of the description of inclusion of medicinal products and means of …

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Name of the medicinal product

WEBThe Agency will evaluate the names again. The Applicant can submit new proposals at any time. If the Applicant wants to change the name for already authorised medicinal …

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Sizes of state fees

WEBThe Resolution No. 1458 of the Government of the Republic of Lithuania of 15 December 2000 „Regarding approval of concrete State fee and the rules of payment and return of …

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Contact information

WEBAddress:. State Medicines Control Agency Studentų str. 45A 08107, Vilnius Lithuania. Tel. +370 5 263 92 64 Fax. +370 5 263 92 65 E-mail: [email protected] Website: …

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Marketing authorization fees

WEBMarketing Authorisation fees are confirmed by the Legal Act of Government of Republic of Lithuania (December 15, 2000, No. 1458). New valid version ((in force since 16 07 2021, …

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Marketing authorisation

WEBDownload. Application for the common Polish and Lithuanian labelling procedure. Download. Application for granting marketing authorisation for homeopathic medicinal …

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Information for healthcare specialists or patients organisations

WEB1. Providing comments for ongoing evaluations. According to the Order No. 159 of the Minister of Health of the Republic of Lithuania of 5th April 2002 ““Regarding approval of …

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Information about fees

WEBInformation about fees. Please by kindly informed that as fees are paid to State Tax Inspectorate (STI) under the Ministry of Finance of the Republic of Lithuania there is …

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Requirements applied for writing of prescriptions of other EU …

WEBinformation about elements to be included into prescribtions which are issued in the member state other than the member state in which medicinal product, medical device …

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Good distribution practice

WEBGood Distribution Practice (GDP) Good Distribution Practice (GDP) is a part of the quality assurance process that ensures that the quality of medicines is maintained at all stages …

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Good manufacturing practice

WEBQuality assurance of medicinal products. In the development, manufacture and testing of medicinal products in the European Union (EU), the pharmaceutical industry is subject …

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Summary product characteristic, labelling, package leaflet

WEBSummary products characteristic. Template for Summary product characteristic, labelling, package leaflet; Template for labelling, package leaflet for homeopathic medicinal products

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