Revision history of "Development of the research laboratory in Vetos-Farma sp z o.o." (Q94410)

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13 October 2024

  • curprev 16:0216:02, 13 October 2024DG Regio talk contribs 61,629 bytes −1 Changed label, description and/or aliases in pt
  • curprev 16:0216:02, 13 October 2024DG Regio talk contribs 61,630 bytes +24 Set a claim value: summary (P836): O projeto «Desenvolvimento do Laboratório de Investigação em Vetos-Farma sp z o.o.» diz respeito à aquisição de um analisador da dimensão das partículas com o qual é possível validar a dimensão das partículas dos componentes dos produtos em desenvolvimento. Ao assegurar que essa análise é possível, o requerente poderá desenvolver e certificar novos produtos no Instituto de Registo e Autorização de Medicamentos e Dispositivos Médicos. A sua introduçã...

7 March 2024

15 January 2024

13 December 2023

10 June 2023

24 May 2023

2 March 2023

  • curprev 23:0223:02, 2 March 2023DG Regio talk contribs 58,075 bytes +516 Changed label, description and/or aliases in da, it, sk, et, lv, cs, es, el, fr, de, hu, bg, ga, ro, sv, fi, pt, lt, hr, nl, sl, mt, and other parts

19 October 2022

26 July 2022

  • curprev 08:2408:24, 26 July 2022DG Regio talk contribs 56,737 bytes +34,425 Changed label, description and/or aliases in da, el, hr, ro, sk, mt, pt, fi, sl, cs, lt, lv, bg, hu, ga, sv, et, nl, fr, de, it, es, and other parts: Adding translations: da, el, hr, ro, sk, mt, pt, fi, sl, cs, lt, lv, bg, hu, ga, sv, et,

19 January 2022

16 January 2022

16 December 2021

7 December 2021

30 November 2021

  • curprev 22:5922:59, 30 November 2021DG Regio talk contribs 14,722 bytes +1,803 Created claim: summary (P836): Le projet «Développement du laboratoire de recherche à Vetos-Farma sp z o.o.» concerne l’achat d’un analyseur de granulométrie, avec l’aide duquel il est possible de valider la taille des particules des substances constituantes des produits en cours de développement. En veillant à ce que cette analyse puisse être effectuée, le demandeur sera en mesure de développer et de certifier de nouveaux produits au Bureau de l’enregistrement et de l’autori...
  • curprev 22:5922:59, 30 November 2021DG Regio talk contribs 12,919 bytes +126 Changed label, description and/or aliases in fr: translated_label

29 October 2020

15 October 2020

  • curprev 21:5121:51, 15 October 2020DG Regio talk contribs 13,233 bytes +122 Changed label, description and/or aliases in 1 language: translated_label
  • curprev 21:5121:51, 15 October 2020DG Regio talk contribs 13,111 bytes −116 Changed label, description and/or aliases in 1 language: remove_english_label
  • curprev 21:5121:51, 15 October 2020DG Regio talk contribs 13,227 bytes +1,679 Created claim: summary (P836): The project “Development of the Research Laboratory in Vetos-Farma sp z o.o.” concerns the purchase of a particle size analyser with which it is possible to validate the particle size of the components of the products being developed. By ensuring that such analysis is possible, the applicant will be able to develop and certify at the Office for Registration and Authorisation of Medicinal Products and Medical Devices new products. Introducing the...
  • curprev 21:5121:51, 15 October 2020DG Regio talk contribs 11,548 bytes −1,195 Removed claim: summary (P836): The project ‘Development of a laboratoorium in Vetos-Farma sp z o.o.’ refers to the purchase of a particle size analyser by which the particle size of the components of the products being prepared can be validated. By ensuring that such analysis is possible, the applicant will be able to develop and certify with the Office for Registration and Marketing of Medicinal Products, medical devices, new products. Introducing them in the company’s bid...

16 July 2020

22 June 2020

10 June 2020

6 June 2020

26 March 2020

6 March 2020

  • curprev 07:1707:17, 6 March 2020DG Regio talk contribs 11,021 bytes +1,195 Created claim: summary (P836): The project ‘Development of a laboratoorium in Vetos-Farma sp z o.o.’ refers to the purchase of a particle size analyser by which the particle size of the components of the products being prepared can be validated. By ensuring that such analysis is possible, the applicant will be able to develop and certify with the Office for Registration and Marketing of Medicinal Products, medical devices, new products. Introducing them in the company’s bid w...

24 February 2020

18 February 2020

31 January 2020

14 January 2020