Resources – Viglya: promoting science, honoring life

EMA establishes Cancer Medicines Forum with academia to optimise cancer treatments in clinical practice

EMA, in collaboration with the European Organisation for Research and Treatment of Cancer (EORTC), has launched the Cancer Medicines Forum (CMF). Bringing together representatives from academic organisations and the European medicines regulatory network, the forum aims at advancing research into optimising cancer treatments and will contribute to foster high standards in cancer care in the European Union (EU). [...]

editor2022-04-06T09:27:29+00:0006.04.2022|Regulatory Affairs, Resources|

(Cas) AEMPS Los problemas de suministro que más afectan al paciente suponen un 0,2% de los casos

Sorry, this entry is only available in European Spanish. For the sake of viewer convenience, the content is shown below in the alternative language. You may click the link to switch the active language. Los problemas de suministro de medicamentos de impacto mayor, es decir, aquellos que causan un mayor trastorno a los pacientes, suponen [...]

editor2022-03-10T11:58:05+00:0010.03.2022|Resources|

EMA: Increase in manufacturing capacity for Vaxzevria (previously COVID-19 Vaccine AstraZeneca)

EMA’s human medicines committee (CHMP) has approved a scale up of manufacturing of Vaxzevria (previously COVID-19 Vaccine AstraZeneca). An existing manufacturing site operated by Universal Farma in Guadalajara, Spain, will add a second filling line for the finished product. This change is expected to support the continued supply of Vaxzevria, including for donations to third [...]

editor2022-01-25T13:46:45+00:0025.01.2022|Drug Development Strategy, Resources|

Sending our warmest wishes to you and your love ones, from the #Viglya Team

editor2021-12-22T19:32:01+00:0022.12.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects - Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-04-12T21:35:07+00:0012.04.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects - Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-04-06T20:25:32+00:0006.04.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects - Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-03-31T09:57:07+00:0031.03.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects – Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-03-25T20:49:45+00:0025.03.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects – Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-03-22T19:31:23+00:0022.03.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist based in Barcelona

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects - Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-03-15T17:52:12+00:0015.03.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Pharmacovigilance Specialist

Job Title Pharmacovigilance Specialist Job Summary Under the supervision of the Head of Pharmacovigilance, the position is responsible for supporting the Viglya activities in the following activities and roles. Primary Duties and Responsibilities Deputy EU QPPV for assigned projects. Local (deputy) QPPV for assigned projects - Spain. Project Lead for assigned projects. Maintain Safety Management [...]

editor2021-03-11T17:13:41+00:0011.03.2021|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya’s team send you our warmest wishes for 2021

editor2020-12-24T10:13:08+00:0024.12.2020|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

We at Viglya send our fondest wishes flying to you

editor2019-12-18T20:47:50+00:0019.12.2019|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya Team wishes you a Happy Fall

editor2019-09-26T19:01:13+00:0026.09.2019|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya Team wishes you a Happy Spring!

editor2018-03-22T22:52:22+00:0023.03.2018|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya Team wishes you a dazzling holiday season and a happy 2018!

editor2017-12-20T21:46:55+00:0020.12.2017|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

Infarmed: Conclusão da migração dos materiais educacionais e das comunicações dirigidas aos profissionais de saúde para a Infomed

Foi concluída a migração dos materiais educacionais e das comunicações dirigidas aos profissionais de saúde para a Infomed - Base de dados de medicamentos do Infarmed. Deste modo, os materiais educacionais e as comunicações dirigidas aos profissionais de saúde passam a estar disponíveis nas fichas dos respetivos medicamentos no Infomed. Os materiais educacionais surgem da necessidade [...]

editor2017-08-08T23:22:56+00:0009.08.2017|Regulatory Affairs, Resources|

The Viglya Team wishes you a Happy Spring!

editor2017-03-29T21:04:56+00:0029.03.2017|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya’s team wishes you a profoundly inspiring 2017

editor2016-12-19T20:03:22+00:0020.12.2016|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|

The Viglya team wishes you a Happy Fall

editor2016-12-11T18:33:47+00:0023.09.2016|Drug Development Strategy, Partnership, Pharmacovigilance, Quality System and Audit, Regulatory Affairs, Resources, Responsibility, The Company, Training|