Quality Control & Quality Assurance

Biotech, pharmaceutical, medical device, and CROs turn to Gemini Staffing for critical resources in quality assurance, regulatory affairs, and compliance functions.

Pharmacovigilance consultants holds clinical trials to use best practices, protecting patients from harm and quantifying risk relative to benefit of the use of the sponsor company’s product. For these reasons, a pharmacovigilance consultant is a critical resource. Gemini Staffing places highly vetted candidates for drug safety and pharmacovigilance positions.

Pharmacovigilance consultants holds clinical trials to use best practices, protecting patients from harm and quantifying risk relative to benefit of the use of the sponsor company’s product. For these reasons, a pharmacovigilance consultant is a highly critical resource. Gemini Staffing places highly vetted candidates for drug safety and pharmacovigilance positions.

The Regulatory Affairs organization within a biotech/pharmaceutical/medical device company holds the overall responsibility of ensuring that the sponsor company adheres to and complies with all regulations and laws set forth by the United States Food and Drug Administration (FDA) pertaining to the company’s product. Regulatory Affairs organizations are comprised of people with titles such as: […]