GMP Compliant Pharmaceutical Logistics

Pharmaceutical Lab Moving Services

GMP & FDA Compliant Relocation for Pharma Facilities

Pharmaceutical laboratory relocations demand the highest level of regulatory compliance, documentation, and procedural precision. Our team specializes in GMP-compliant lab moves for pharmaceutical manufacturers, contract research organizations (CROs), and bioanalytical labs. We understand validation requirements, chain-of-custody obligations, and the impact that equipment moves have on regulatory filings.

GMP & GLP compliant protocols FDA inspection-ready documentation Chain-of-custody management Cleanroom equipment relocation

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Licensed & Insured· FDA Compliant· Nationwide

What's Included

GMP & GLP compliant protocols
FDA inspection-ready documentation
Chain-of-custody management
Cleanroom equipment relocation
Cold chain & controlled storage
21 CFR Part 11 documentation
IQ/OQ/PQ validation support
Equipment requalification support
Serialized equipment tracking
DEA compliant procedures
Change control documentation
CMC change assessment support

Our Process

How It Works

1

Regulatory Review

We review your change control requirements and develop a move protocol that satisfies your quality system and regulatory obligations.

2

GMP Documentation

All equipment moves are fully documented per GMP standards, including equipment IDs, condition assessments, and environmental data.

3

Compliant Execution

Our certified team executes the move with trained personnel, appropriate PPE, and environmental monitoring throughout.

4

Requalification Support

We support IQ/OQ/PQ protocols and provide complete move documentation packages to support your regulatory filings.

FAQ

Frequently Asked Questions

Can you move equipment for FDA-regulated pharmaceutical facilities?

Yes. We are experienced in moving equipment for FDA-regulated pharmaceutical facilities. We provide comprehensive move documentation to support change control and regulatory filings.

Do you support equipment requalification after moves?

Yes. We provide detailed move documentation packages that support IQ, OQ, and PQ protocols. We can also coordinate with your qualified persons and validation teams.

Can you relocate cleanroom equipment?

Yes. We have specialized protocols for moving equipment to and from cleanroom environments, including gowning compliance, contamination control, and proper equipment decontamination.

What is change control and how do you support it?

Change control is a pharmaceutical quality system requirement for documenting any changes to equipment or processes. We provide complete documentation of the move for your change control record, including equipment condition before and after.

Do you handle controlled substances or DEA-regulated equipment?

We follow DEA regulations for transport of DEA-registered equipment and coordinate with your DEA registered officer for all relevant moves.