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June 16, 2025

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June 16, 2025
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Margarida Tapadas

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EMA’s expectations on the use of third-party GMP audit reports

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January 31, 2024

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Owlpharma becomes a member of the 3PARL

November 24, 2023

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GCP Audits - A new piece in our compliance puzzle

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Owlpharma's Quality Management System - Certification ISO 9001:2015

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Ricardo Andrade

Inauguração da nova sede

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Desafios atuais de Farmacovigilância - Edição 2024

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Lígia Ferreira

New HMA-EMA catalogues of real-world data sources and studies

January 31, 2024

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Mariana Pinto

Owlpharma becomes a member of the 3PARL

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June 16, 2025

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Margarida Tapadas

Planning to Export or Import Medicinal Cannabis? Get Ready for INFARMED’s New Requirements

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André Luz

European Shortages Monitoring Platform (ESMP) Goes Live

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February 28, 2025

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Helena Marques

New National Regulations on Medicines Export and Availability

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November 21, 2024

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EMA’s expectations on the use of third-party GMP audit reports

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European Shortages Monitoring Platform (ESMP) Goes Live

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GMDP, Legislation

Annex 1 - Manufacture of Sterile Medicinal Products

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August 29, 2022

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OWL

PME Excelência '21

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December 14, 2022

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OWL

knOWLedge – O programa de formações Owlpharma

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April 27, 2023

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OWL, GMDP, Legislation

Anexo 1 - Mudanças e desafios no fabrico de medicamentos estéreis

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May 2, 2023

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OWL

A new project – Future Headquarters

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June 9, 2023

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OWL, GMDP

AuditSearch - Owlpharma's new tool

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July 31, 2023

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OWL

DIA Marketplace

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September 6, 2023

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Pharmacovigilance

Desafios atuais de Farmacovigilância - Edição 2023

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September 21, 2023

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GMDP; Regulatory

MDR extension period – Where do you stand now?

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September 22, 2023

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OWL, Pharmacovigilance

DESAFIOS ATUAIS DE FARMACOVIGILÂNCIA - Resumo da 1ª edição

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November 23, 2023

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OWL, GMDP

GCP Audits - A new piece in our compliance puzzle

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November 24, 2023

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OWL

Plano de formações knOWLedge 2024

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January 16, 2024

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OWL, GMPD

Owlpharma becomes a member of the 3PARL

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January 31, 2024

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OWL, Medical & Scientific, Pharmacovigilance

New HMA-EMA catalogues of real-world data sources and studies

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February 23, 2024

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Legislation, Regulatory

Latest news on Advertisement of Medicinal Products in Digital Channels in Portugal

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March 12, 2024

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Legislation , Medical & Scientific

Environmental Risk Assessment - The long-awaited updated guideline

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April 8, 2024

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Legislation

New Decree-Law for Medical Devices in Portugal

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April 15, 2024

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Legislation

New MDCG guidance: Investigator’s Brochure and Summary of Safety and Performance Template

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April 29, 2024

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OWL

Fórum de Diretores Técnicos de Distribuição

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May 17, 2024

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GMDP

Handling API manufacturers: Insights from the New CEFIC-APIC Guide and Owlpharma recent experience

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May 20, 2024

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Owl; Pharmacovigilance

Desafios atuais de Farmacovigilância - Edição 2024

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May 27, 2024

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GMDP

The legal framework of medicinal cannabis in Portugal

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June 13, 2024

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Regulatory

SCCS - Scientific Advice on Titanium dioxide (TiO2)

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July 1, 2024

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New MDCG Guidance: Clinical evaluation of orphan medical devices

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July 23, 2024

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Legislation; Regulatory

Updates in the labelling of fragrance allergens in cosmetics

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August 21, 2024

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Regulatory

New European Health Technology Assessment Framework for 2025

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September 11, 2024

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OWL

Inauguração da nova sede

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September 17, 2024

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World Patient Safety Day

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September 17, 2024

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Owlpharma's Quality Management System - Certification ISO 9001:2015

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October 4, 2024

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Regulatory, Legislation

Annual Price Revision for 2025

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November 18, 2024

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Pharmacovigilance; Legislation

Risk Minimisation Measures - GVP Latest Updates

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November 21, 2024

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Legislation; Regulatory

New National Regulations on Medicines Export and Availability

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February 28, 2025

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GMDP, Regulatory, Legislation

European Shortages Monitoring Platform (ESMP) Goes Live

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March 5, 2025

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GMDP

EMA’s expectations on the use of third-party GMP audit reports

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April 22, 2025

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Legislation; Regulatory

Planning to Export or Import Medicinal Cannabis? Get Ready for INFARMED’s New Requirements

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June 16, 2025

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