Saskia Lacroix
About Saskia Lacroix
Saskia Lacroix is a regulatory compliance specialist in the pharmaceutical industry, currently working at UPSA and Bristol-Myers Squibb. She holds a Master's Degree in Regulatory Affairs from Université Lille II.
Current Position at UPSA
Saskia Lacroix is currently serving as the Responsable CMC at UPSA in Agen, France. She has been dedicated to this role since February 2004, where she specializes in Chemistry, Manufacturing, and Controls (CMC) within the pharmaceutical industry. Her extensive experience ensures compliance with regulatory standards and effective management of CMC activities.
Role at Bristol-Myers Squibb
Saskia Lacroix also works at Bristol-Myers Squibb as the Responsable Conformitã Rã Glementaire Site et CMC in New York, New York, United States. In this position, she oversees regulatory compliance and CMC processes, ensuring that the company adheres to regulatory standards and guidelines.
Educational Background
Saskia Lacroix holds a Master’s Degree in Regulatory Affairs, having studied Drug Regulation in the European Union at Université Lille II. Her academic background equips her with profound knowledge in regulatory affairs, particularly in the intricacies of drug regulation within the European Union.
Expertise in Regulatory Affairs
Saskia Lacroix brings a wealth of expertise in regulatory affairs, with a particular focus on Chemistry, Manufacturing, and Controls (CMC). Her specialization enables her to navigate the complexities of regulatory environments, particularly within the European Union, ensuring that pharmaceutical products meet stringent regulatory standards.
Based in Nouvelle-Aquitaine, France
Saskia Lacroix is based in Notre-Dame-de-Sanilhac, Nouvelle-Aquitaine, France. Her professional roles span international boundaries, reflecting her capacity to manage and oversee regulatory and CMC functions across multiple locations and regulatory jurisdictions.