Fragmented safety programs leave gaps.
In pharma, safety isn’t just an OSHA requirement, it’s a GMP requirement.
USP builds annual safety programs for pharmaceutical manufacturers, biotech firms, and clinical research operations, from chemical exposure compliance to cleanroom safety protocols. One partner, every coverage gap closed.
RECENT RESULTS
31%
$30K+
55+
WHAT’S AT STAKE
A safety violation in pharma can trigger an FDA action — not just an OSHA citation.
Pharmaceutical manufacturing sits at the intersection of OSHA, FDA, and DEA regulatory oversight.
Chemical exposure events, containment failures, and PPE compliance gaps don’t just generate OSHA citations, they can trigger FDA 483 observations and Warning Letters that halt production. The cost of a single audit finding in pharma dwarfs the cost of any OSHA fine.
TRUSTED BY
SERVICES FOR PHARMACEUTICAL
Everything a pharmaceutical operation needs. In one program.
Safety Consulting & Training
Occupational Health & Wellness
Emergency & Technical Rescue
Safety Staffing
Regulatory Compliance
View All Services
HOW WE DO IT
A program designed to survive an FDA audit — not just an OSHA inspection.
Pharma safety programs live or die in the documentation. USP builds annual programs with audit-ready recordkeeping, GMP-aligned procedures, and regulatory update cycles built in, with one program manager who understands the difference between a 483 observation and a Warning Letter.
OUR PROCESS
CLIENT RESULTS
What a United Safety Professional program looks like in practice.
ANNUAL SAFETY PROGRAM
Specialty Pharma Manufacturer Passes FDA Inspection with Zero Safety-Related Observations
FROM THE FIELD
What our clients are saying after one year
Other industries we work with
INSIGHTS & RESOURCES
Compliance guides, regulatory updates, industry resources.
GET STARTED
Let’s build your annual safety program.
Tell us about your operation. We’ll respond within one business day with a program assessment framework tailored to your industry and headcount.