PHAGECON - Serviços e Consultoria Farmacêutica Ltd
Portuguese pharmaceutical consultancy providing regulatory affairs, scientific affairs, pharmacovigilance, quality assurance, training, clinical trials and translation services.
Last updated September 29, 2026
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Overview
PHAGECON - Serviços e Consultoria Farmacêutica Ltd is a Portuguese consultancy dedicated to the pharmaceutical industry, founded in January 2006 with national capital. Headquartered in Lisbon at Avenida José Malhoa, Malhoa Plaza, the company positions itself as a strategic partner for pharmaceutical, biotech and medical device companies, offering a broad portfolio of specialised services across the product life cycle. Its core service lines include Regulatory Affairs, Scientific Affairs and Market Access, Pharmacovigilance, Quality Assurance, Training Services, Clinical Trials and Translations. The firm describes its approach as flexible, tailored and results-oriented, with a mission to provide innovative solutions that help clients meet regulatory requirements and achieve market access. PHAGECON operates nationally and internationally, supporting companies in navigating the highly regulated European pharmaceutical environment. Its stated values are Quality, Confidentiality, Excellence, Efficiency and Professionalism. The company's regulatory affairs practice covers strategic planning for marketing authorisation submission, gap analysis, dossier elaboration and submission, product launch and maintenance activities. Its quality assurance services include licensing of entities, Qualified Person services, and implementation of Quality Management Systems compliant with standards such as ISO 9001:2015 and ISO 13485:2016. PHAGECON also provides pharmacovigilance system implementation and ongoing activities, medical writing, pharmacoeconomics support, and clinical trial management. The company is privately held and remains active as of its latest public communications.
History
PHAGECON - Serviços e Consultoria Farmacêutica Ltd was founded in January 2006 as a Portuguese company formed by national capital, dedicated to serving the pharmaceutical industry. The company emerged in response to the growing demand for specialised regulatory and quality services in the highly regulated European pharmaceutical sector. From its base in Lisbon, at Avenida José Malhoa in Malhoa Plaza, PHAGECON developed a portfolio of consulting services covering regulatory affairs, scientific affairs, pharmacovigilance, quality assurance, training, clinical trials and translations. Regulatory Affairs was the main reason for the company's inception, driven by increasingly tight requirements in Europe and other continents. Over the years, PHAGECON expanded its activities to operate at both national and international levels, supporting various companies strategically. The company has continuously developed its service offerings to keep pace with evolving legislation and industry standards, including quality management systems aligned with ISO 9001:2015 and ISO 13485:2016, Good Manufacturing Practices and Good Distribution Practices. Its stated vision is to build a solid company with a worldwide presence, recognised for its expertise and contributing to the success of the pharmaceutical industry through innovative approaches and personalised services.
- 2006
PHAGECON founded in January 2006 as a Portuguese company with national capital.
Company expands to operate at national and international level, supporting various companies strategically.
PHAGECON offers a complete portfolio of services including Regulatory Affairs, Scientific Affairs, Pharmacovigilance, Quality Assurance, Training, Clinical Trials and Translations.
Products and positioning
Strategic partner for the pharmaceutical industry, offering flexible, tailored and innovative solutions with guaranteed results.
Regulatory Affairs
Strategic planning for MA submission, gap-analysis, dossier elaboration, submission, product launch and maintenance activities.
Scientific Affairs & Market Access
Technical reports, medical writing, pharmacoeconomics support, medical devices and other products.
Pharmacovigilance
Implementing a complete PV system, performing mandatory ongoing activities, and other punctual activities.
Quality Assurance
Quality Management Systems, Good Manufacturing Practices, Good Distribution Practices, audits, Qualified Person service.
Training Services
Training sessions for 2026 and specialised, differentiated training.
Clinical Trials
CT management and strategy, clinical operations excellence, end-to-end solutions for pharmaceutical and biotech services worldwide.
Translations
Available tools and translations we ensure.
Sources5 sources
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