GMP Cleaning Services Built to Protect Product Integrity
Cleaner workflows lead to safer outcomes and full GMP compliance.
Start Your GMP Compliance Plan
Quality control fails when ISO compliance is broken.
Even minor lapses can disrupt production and delay breakthroughs.
In life sciences, even a small lapse in cleanliness can shut down operations, delay timelines, and damage credibility. When ISO standards are missed, research and manufacturing lose their foundation. Protect your teams, your outcomes, and every advancement that depends on a cleanroom built to perform.
GMP cleaning that helps science reach the people who need it.
Built-in compliance protects your work, your team, and your outcomes.
Your breakthroughs deserve an environment that meets the highest standards of cleanliness and safety. Servicon’s GMP cleaning services reduce contamination risk, support audit readiness, and keep your focus on advancing life-changing work with confidence.
Built on GMP expertise, trusted by critical industries since 1973.
Consistent cleaning performance that meets the highest regulatory demands.
In high-stakes environments, contamination control is more than a task. It is a discipline rooted in experience, precision, and accountability. Servicon brings decades of focused expertise to GMP facilities, delivering cleaning programs that align with strict protocols and support operational momentum from day one.
Three steps to launch your GMP cleaning plan.
Designed to get you operational, compliant, and audit-ready.
Step One:
Talk with a Servicon GMP expert to discuss your facility, protocols, and goals.
Step Two:
Set up a site visit and receive a tailored proposal with clear scope and pricing.
Step Three:
Implement a high-performance program aligned with ISO and GMP standards.
Testimonial
Earning a client's trust is our greatest privilege.
Struggling to find qualified GMP cleaning staff?
The right people start with the right process.
Download our guide to see how Servicon recruits and trains GMP technicians with the mindset, protocols, and precision your facility demands.
Your Questions About Life Sciences Cleaning, Answered.
What we do, how we do it, and what sets our teams apart.
What cleanroom and GMP services does Servicon provide for life sciences?
Servicon offers full-service GMP cleaning, maintenance, and contamination control for highly regulated life sciences environments. We tailor every program to meet the specific compliance and sterility needs of each space.
Our services support:
- GMP cleanrooms – Critical environments where precise, validated cleaning is essential
- CNC areas – Non-classified zones that support GMP production and storage
- Common areas – High-traffic spaces requiring infection prevention and containment
- Warehouses – Controlled storage environments with strict cleanliness standards
- Building surrounds – Exterior cleaning to reduce the risk of tracked-in contamination.
Every facility has unique compliance expectations. Servicon matches qualified, site-trained technicians to each zone, ensuring protocols are met with precision.
What types of life sciences facilities require GMP cleaning?
Servicon supports a wide range of life sciences organizations where cleanliness is essential for safety, sterility, and regulatory approval.
We serve facilities including:
- Biotechnology labs
- Pharmaceutical production and development sites
- Biopharmaceutical manufacturing plants
- Medical device testing environments
- Clinical trial and genomics research centers.
Each facility type has distinct compliance requirements. Servicon designs cleaning programs that meet those standards and support uninterrupted operations.
What is GMP cleaning, and why is it critical?
GMP stands for Good Manufacturing Practice, which applies to environments where regulated products are developed, tested, or produced.
GMP cleaning is critical because it:
- Prevents contamination in sensitive production environments
- Ensures compliance with FDA and industry regulations
- Protects patients and end users from exposure risks
- Maintains audit readiness with validated procedures.
GMP cleaning is a slow, methodical, and fully documented process. Every task follows strict protocols and must be traceable to support compliance.
What is the difference between GMP and GDP in cleanroom cleaning?
GMP refers to the methods and procedures used to clean and maintain facilities to meet quality standards. GDP, or Good Documentation Practice, refers to the process by which cleaning tasks are accurately and thoroughly documented.
Here’s how they work together:
- GMP focuses on doing the right task using the correct tools, methods, and timing
- GDP ensures everything is recorded clearly, accurately, and according to SOPs
- Both are required for FDA audits, and both impact compliance outcomes.
Servicon’s technicians are trained to excel in both areas, combining precision cleaning with complete, regulation-ready documentation.
What training do GMP cleanroom cleaning technicians receive at Servicon?
Servicon follows a structured, site-specific training process to prepare every technician for GMP environments.
Our process includes:
- Vetting and hiring individuals with the right mindset for regulated spaces
- Orientation aligned with Servicon’s safety, quality, and compliance culture
- Targeted GMP protocols training
- A facility-specific overview of site SOPs and standards
- At least six hours of supervised, on-site training before independent work begins.
Technicians earn GMP credentials only after demonstrating readiness, attention to detail, and procedural accuracy.
What are ISO cleanroom classifications, and how does Servicon support them?
ISO classifications define the required particle control levels in cleanrooms. The lower the ISO number, the more stringent the standards.
Servicon supports ISO-classified environments by:
- Adhering to client SOPs that align with ISO 14644 standards
- Matching cleaning frequency and technique to each classification level
- Ensuring contamination control through proper gowning, tools, and documentation
- Training teams to meet requirements for even the most critical cleanrooms.
We maintain cleanroom integrity across ISO levels to help your facility stay compliant, audit-ready, and fully operational.