PharmaLogika is dedicated to maintaining high standards of quality and accuracy in the life sciences sector, focusing on various regulatory frameworks and compliance practices. The company offers services related to Computer System Validation, ensuring adherence to regulations for pharmaceuticals, biologics, and medical devices. They provide concise reference materials on Current Good Manufacturing Practices (CGMP) and guidelines for dietary supplements, which include aspects of manufacturing, distribution, labeling, and premarket notification. Additionally, PharmaLogika assists clients with FDA establishment inspections and compliance remediation, emphasizing their commitment to Good Laboratory Practice (GLP).

In the realm of clinical studies and product development, PharmaLogika specializes in managing clinical trials and overseeing research and development processes. Their services encompass product targeting and marketing, clinical study development, and education for both practitioners and patients. The company ensures compliance with Good Clinical Practice (GCP) and offers comprehensive support for manufacturing operations, whether through contract manufacturing organizations (CMOs) or internal processes. Their expertise extends to clinical trial management on a global scale, as well as packaging and labeling, highlighting their multifaceted approach to advancing the life sciences industry.

United States

The mission of PharmaLogika is to provide quality services and the highest level of expertise to start-up as well as established industry leaders from discovery, through clinical trials, to commercialization of ideas. Our goals include the deployment and management of consulting teams utilizing our online products, while maintaining the lowest possible overhead cost structures. Our target audience is primarily but certainly not exclusively small to medium size businesses within the Pharmaceutical, Biotech, and Medical Device industries.

PharmaLogika

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