AEGISANA

Aegisana

@aegisana

Alcobendas, Madrid
https://aegisana.com
Pharmaceutical Manufacturing

Overview

About Aegisana

Aegisana is at the forefront of the evolution of life sciences services with efficient and effective Pharmacovigilance and Auditing solutions. We create value and confidence for our customers through a combination of technical expertise, applied useful technology and outstanding customer experience.

Our extensive Clinical Safety and Pharmacovigilance services also encompass Veterinary and Cosmetics to provide a wide offering and continuity of provision for clients with products across these areas.

We have a comprehensive Auditing and Quality Assurance service that covers GCP, GVP, VGVP, GMP and GDP consultancy solutions, and can also offer practical support from inspection readiness through to audits and inspections, remotely or on-site.

Headquartered in Madrid, we also have technical centres in Barcelona and Lisbon and we’re expanding rapidly in other locations across Europe. Our wide partner network allows us to undertake client projects spanning multiple countries and authorities across Europe and beyond.

Above all, we never forget our core purpose as your trusted patient safety partner, and how Aegisana, which translates to ‘health protection’, embodies our approach and ethos.

Headquarters

Alcobendas, Madrid

Website

https://aegisana.com

Company Size

11-50 employees

Industry

Pharmaceutical Manufacturing

Company Type

Privately Held

Founded

2019

Specialties

Pharmacovigilance, Cosmetovigilance, Medical Writing, Veterinary Vigilance, Clinical Safety, GMP Compliance & Auditing, GCP Compliance & Auditing, GVP/VGVP Compliance & Auditing, GMP Compliance & Auditing, GDP Compliance & Auditing, LPPV, Case Intake, SOPs, PSMF Management, EU QPPV, Risk Management, Literature Monitoring, Regulatory Intelligence, Signal Management, Safety Database, Responsible Persons, Qualified Persons, Vendor Management, Gap Analysis, Deviation & CAPA Management, Process Validation, Change Control, Quality & Technical Agreements, Supplier Qualification, Audit Program Management, Manufacturing Transfer, Product Quality Review, and BMR/BPR Creation & Review

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