Xevalics Consulting helps pharmaceutical, biotech, and agroscience organizations build compliance programs that withstand regulatory inspection.

Our practice spans four core areas: CSV/CSA & Validation Programs, Digital Lab Transformation (Benchling ELN, Veeva DMS), AI/ML Compliance & Governance, and Data Integrity & Document Management. We work across GMP, GLP, and GCP-regulated environments, serving clients navigating FDA, EPA, OECD, EMA, and international regulatory frameworks.

Our approach is risk-based and practitioner-led. Every control we design exists to protect the business, the patient, and the data — not because it was copied from a template. We bring 25+ years of biopharmaceutical validation experience to every engagement, from laboratory standalone systems to enterprise platform deployments.

Xevalics is led by Ricardo Torres-Rivera, PMP — SQA Quality College Instructor, Chair of the SQA CVIC Steering Committee & AI Subcommittee, and contributing author at Pharmaceutical Online. His current focus: helping organizations understand that GenAI can accelerate generation, but the expert must govern judgment.

Xevalics Consulting is an NMSDC-certified minority-owned business headquartered in Minneapolis, Minnesota.

Bold Thinking. Precise Execution.

✉ info@xevalics.com  |  ☎ (787) 603-2946  |  xevalics.com

Xevalics Consulting

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