Company code 191351864
Žirmūnų str. 139A, Vilnius, Lithuania
E-mail: vvkt@vvkt.lt,
Phone: +370 5 263 92 64
Fax: +370 5 263 92 65






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Pavadinimas
10.3.3 List of Standard Terms for pharmaceutical Dosage forms, for Containers, closures and administration devices, for Combined terms and for Routes and methods of administration.
10.3.1. List of names for substances for pharmaceutical use and preparations presented in European Pharmacopoeia
10. The list of Recommended International NonProprietary Names for pharmaceutical substances (INN) in English, Lithuanian and Latin languages
Commission Regulation (EC)No 1084/2003
Commission Regulation (EC)No 1084/2003
Good manufactures practice requirements
Composition of names of medicinal products
Commission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use
Application form for change in classification to a marketing authorisation
1.1 Law of pharmacy
2.1.1. Rules for granting marketing authorization for medicinal products
5.1. The Law on Ethics of Biomedical Research
4.4 SMCA requirements for Post-Authorisation Safety Studies (only in Lithuanian)
4.1. ADR reporting rules for health care profesionals, pharmacists and patients (only in Lithuanian)
11.1. The rules of reporting about sales of medicinal products packages and remainders of medicinal products packages in the Republic of Lithuania (only in Lithuanian)
6.1. Law on advertising
7.5.2. On the Approval of the Regulations of Issuing Licences (only in Lithuanian)
6.2. Law on competition
2.3.4. Regarding sale out of packages of medicinal products
4.6. Regarding Pharmacovigilance Inspections (only in Lithuanian)
3.2. Rules on supply to the market of unauthorized medicinal products of the necessary assortment (only in Lithuanian)
3.1. Rules on obtaining of nominal medicinal products prescribed for individual patient (only in Lithuanian)
6.4. Rules on the advertising of medicines (only in Lithuanian)
7.2.1 Law on the Control of Narcotic and Psychotropic Substances
6.3. Law on Provision of Information to the Public
7.3.1. Schedule of Narcotic drugs and pshychotropic substances (only in Lithuanian)
5.13. Order No.1A-72 of 26 Jan 2011 of the Director of the State Medicines Control Agency under the Ministry of Health of the Republic of Lithuania “Regarding confirmation of rules of inspections regarding conduct of clinical trials of medicinal products, confirmation of forms inspection protocol regarding conduct of clinical trials of medicinal products and confirmation of forms of register of protocols regarding conduct of clinical trials of medicinal products”
2.2.5. Common Baltic Package Guidance
5.11. Order No 1A-91 of 18 Jan 2007 of the Director of the State Medicines Control Agency under the Ministry of Health of the Republic of Lithuania “Regarding confirmation of the description of the requirements applied for preparation of good clinical practice training and composition of programs”
5.5. Order No. 1A-663 of 30 Oct 2006 of the Director of the State Medicines Control Agency under the Ministry of Health of the Republic of Lithuania “Regarding confirmation of the description of the order applied for reporting about undesirable events observed during clinical trials of medicinal products and undesirable reactions to investigated medicinal products”
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