bioconsulting

Our goal is to contribute proactively to a world in which all patients have access to high quality, safe, effective, and more affordable drugs

SERVICES

FACILITY COMPLIANCE

Pharmaceutical companies strive to comply with current good manufacturing practices (cGMPs) and applicable statutes and regulations at their manufacturing plants

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REGULATORY AFFAIRS-CMC

Chemistry, Manufacturing, and Controls (CMC) is an essential and complex part of pharmaceutical regulatory submissions and it is intricately connected to GMPs

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GO-TO-MARKET STRATEGY

Designing a successful market strategy requires a thorough methodology, however, many companies make decisions without the necessary information to assure their success when expanding to new world regions

Learn more

FACILITY COMPLIANCE

Pharmaceutical companies strive to comply with current good manufacturing practices (cGMPs) and applicable statutes and regulations at their manufacturing plants.

Learn more

REGULATORY AFFAIRS - CMC

Chemistry, Manufacturing, and Controls (CMC) is an essential and complex part of pharmaceutical regulatory submissions and it is intricately connected to GMPs.

Learn more

GO-TO-MARKET STRATEGY

Designing a successful market strategy requires a thorough methodology, however, many companies make decisions without the necessary information to assure their success when expanding to new world regions.

Learn more

OUR TEAM

We are a dynamic team of experts passionate about pharmaceutical development and commercialization and its complex regulatory universe

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María José
López
Barragán

PhD
Partner

Antonina
Nikolova

PhD
Partner

Marine
Joly-Battaglini

PharmD
Partner

Yuexia
Li

PhD
Partner

Katerina Deverell

Chem Eng
Partner

OUR TEAM

We are a dynamic team of experts passionate about pharmaceutical development and commercialization and its complex regulatory universe

Learn more

María José
López
Barragán
PhD
Partner

Antonina
Nikolova
PhD
Partner

Marine
Joly-Battaglini
PharmD
Partner

Yuexia
Li
PhD
Partner

Katerina
Deverell
Chem Eng
Partner

Barragán BioConsulting was created in July 2020 with the aim of assisting pharmaceutical and biotech companies to better navigate the complex regulatory framework for the approval of biological products for human use

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Our primary objective is accomplished by transparently sharing our valuable and specific knowledge in biotechnology products quality and extensive experience in facility compliance with our clients, maximizing their chances for drug approval and minimizing their time-to-market

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Our philosophy is inspired by the idea of kaizen: continuous improvement

Our mission is to share with our clients a quality management method that involves the implementation of focused and effective actions to achieve the optimization of all processes in a constantly improving manner