About Us
Experience You Can Count On
QLC offers comprehensive quality and regulatory compliance services that conform to a variety of international standards and regulations including the following:
- Medical Device, Pharmaceutical, IVD, and Biologics
- Quality System Regulation (QSR)
- International Organization for Standardization (ISO)
- Good Laboratory Practice (GLP)
- Good Clinical Practice (GCP)
- Current Good Manufacturing Practice (cGMP)
- International Conference on Harmonization (ICH)
- General Data Protection Regulation (GDPR)
- Data Integrity
- Data Privacy (HIPAA)
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Our ramp up process is designed to empower your team and outfit them with the tools they need to succeed. Talk to us today about how we can support your growth, limit your turnover, and put you on a solid track to success and profit.
President & Principal Consultant
Jacqueline Torfin
Pharmaceutical/Medical Device leader with Masters in Organizational Leadership, scientific background and proven track record with over 30 years of increasingly responsible positions within multi-site global companies. Skilled at working across functions within a matrix organization to obtain optimal business outcomes. Quick to grasp technical concepts and creatively address business challenges.
Certifications include:
- Board of Registry of the American Society of Clinical Pathologists, MT (ASCP): 181187
- American Society for Quality, Certified Quality Auditor
- SGS Pharmaceutical GMP Pharmaceutical certified Auditor
- Applied Quality Systems, Lead ISO auditor and ISO 13485/MDD qualified lead assessor
