Qualipharma is a pharmaceutical consultancy (Lifesciences Compliance & Regulatory) offering global services in the pharmaceutical and bio-health industry. Thanks to its perfectly integrated business units: Regulatory Affairs, GXP and FDA Consulting, Qualification, CSV and GDP, it offers global support to all those sectors that are governed by strict quality parameters: human and veterinary pharmaceuticals, biotechnology, advanced therapies, medical cannabis, medical devices, food supplements, cosmetics, personal care and biocides, hospital and biosafety. With a track record of more than 20 years and a team of more than 150 professionals located in its offices in Madrid, Barcelona, León, Bilbao and Buenos Aires, it provides services to its more than 900 clients while maintaining the values that have always characterised the company: proximity, agility, flexibility, competitiveness and excellence. Qualipharma is considered a leader in technological innovation thanks to its own developments: e-learning, Match Consulting and Qloud. 

e-Learning by Qualipharma, is a platform that offers specialised courses in the industry, and allows you to obtain a dynamic Certification of Pharmaceutical Talent (Bronze, Silver and Gold). 

Match Consulting by Qualipharma is a platform that connects industry projects with professional candidates to achieve the perfect match.

Qloud by Qualipharma is a tool that enables real-time qualification, protocol and reporting to ensure data integrity, eliminate errors and optimise time.

Awarded as Gender Parity Company, its employees evaluated the work environment, reason to be, sustainable development, leadership, professional development and recognition as the main indicators that certify the company as Happy At Work 2023 and Happy Trainee 2024.

QUALIPHARMA

Gabriel Tallada Frotté

Alejandro García

Andrea Navalón Candela

Alvaro Soto Mengotti

This department provides expert guidance and support on Good Practice (GxP) regulations and compliance.

GxP Consulting

This department focuses on managing and optimizing CSV processes and consultations.

CSV Operations

This department focuses on ensuring that systems and equipment are properly commissioned and qualified to meet regulatory and operational standards.

Commissioning and Qualification

This department manages compliance and communication with regulatory bodies to ensure adherence to industry laws and standards.

Regulatory Affairs

This department specializes in the calibration and validation of equipment and processes to ensure compliance with industry standards.

Calibration and Validation

This department focuses on generating revenue through the sale of products or services.

QUALIPHARMA

Org chart

Teams

GxP Consulting

CSV Operations

Commissioning and Qualification

Regulatory Affairs

Calibration and Validation

Sales

Offices

QUALIPHARMA

Org chart

Teams

GxP Consulting

CSV Operations

Commissioning and Qualification

Regulatory Affairs

Calibration and Validation

Sales

Offices

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