What are the key standards biohq adheres to

Updated 9/11/2025

BioHQ adheres to a variety of key standards to ensure consistency, quality, and regulatory compliance in biotechnology operations. Among the critical standards are the International Organization for Standardization (ISO) guidelines, such as ISO 9001 for quality management systems and ISO 13485 for medical devices. Additionally, BioHQ aligns with the Good Laboratory Practice (GLP) regulations, which provide a framework for conducting non-clinical safety studies. The integration of these standards ensures that BioHQ supports robust data integrity, reliable laboratory operations, and high-quality outputs. Furthermore, BioHQ incorporates standards related to data security and privacy, such as the General Data Protection Regulation (GDPR) in the EU and the Health Insurance Portability and Accountability Act (HIPAA) in the United States, ensuring that sensitive information is protected. By adhering to these standards, BioHQ facilitates trust and credibility in biotechnological research and development processes. Key Takeaway: BioHQ aligns with ISO, GLP, GDPR, and HIPAA standards for quality, safety, and data protection.