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Integral to Your Success

Providing Commissioning, Qualification, and Validation (CQV) and Water System Monitoring Services to the Biotechnology & Pharmaceutical Industry. We are passionate about providing quality service to companies that provide life-saving drugs.

About Salent Solutions

Founded in 2019, Salent Solutions was created to ensure exceptional quality services for our clients in the pharmaceutical and biotechnology sectors. Our founder, Stella Lanphear, brings a wealth of experience, dedication, and leadership in Commissioning, Qualification, and Validation (CQV).

Our mission is simple: to provide skilled professionals who become integral to the success of your critical projects. We partner with companies nationwide to support the delivery of life-altering and life-saving therapies.

Client Testimonials

“I had the pleasure of working with Stella Lanphear on one of the most complex and fast-paced projects... Stella demonstrated exceptional leadership skills, ensuring that all team members were aligned and working towards the same goals.”

— Siddharth Bhargava, Associate Director of Validation Engineering at Bristol Myers Squibb

“I want to thank you for the tremendous support you’ve provided me in S12 ECQ Delivery... Thank you for the progress we’ve made and your commitment to ECQ Delivery and S12.”

— Adam Mivelaz, Celgene

Partner With Us

We know that finding the right talent for laboratory and manufacturing support is critical. Let’s connect to discuss your project scope, goals, and how Salent Solutions can help you achieve commercial readiness.

Contact Us Today

Our Core Services

Salent Solutions specializes in high-impact services that ensure compliance, efficiency, and success in biotech and pharmaceutical operations.

CQV Services

Comprehensive Commissioning, Qualification, and Validation services for facilities, equipment, and systems. We ensure your assets meet regulatory standards and are ready for commercial operation.

  • • Facility and equipment commissioning
  • • IQ/OQ/PQ protocols and execution
  • • Risk-based validation strategies
  • • Regulatory compliance (FDA, EMA, etc.)
  • • Project management during CQV phases

Water System Monitoring

Continuous monitoring and validation of purified water (PW), water for injection (WFI), and clean steam systems to ensure consistent quality and compliance.

  • • Routine sampling and trending
  • • Alarm response and deviation management
  • • System qualification and requalification
  • • Data integrity and audit readiness
  • • 24/7 monitoring support

Our Specialized Solutions

Tailored services designed for the unique challenges of the life sciences industry.

Facility Commissioning

End-to-end support for new or renovated biopharmaceutical facilities, ensuring systems are installed and operate as intended.

Equipment Qualification

Development and execution of IQ/OQ protocols for manufacturing and laboratory equipment across all project phases.

Process Validation

Validation of critical manufacturing processes to ensure consistent product quality and regulatory compliance.

Cleanroom Qualification

Airborne particle monitoring, airflow visualization, pressure differentials, and environmental monitoring for ISO-classified spaces.

Water for Injection (WFI) Systems

Design review, qualification, and ongoing monitoring of WFI generation and distribution systems.

Computer System Validation (CSV)

Validation of LIMS, SCADA, MES, and other GxP-critical software systems in compliance with 21 CFR Part 11.

Project Management

Experienced leadership to manage complex CQV timelines, resources, budgets, and stakeholder communication.

Deviation & CAPA Support

Root cause analysis, investigation support, and corrective action planning for validation-related deviations.

Regulatory Audit Readiness

Preparation and mock audits to ensure your validation documentation and practices meet FDA and global standards.

SOP Development

Creation and review of standard operating procedures for validation, monitoring, and quality systems.

Training & Knowledge Transfer

On-site training for client teams to ensure long-term sustainability of validation programs.

Remote Monitoring Support

Flexible, scalable support for water and environmental monitoring programs, including data review and reporting.

2019
Founded
50+
Projects Completed
15+
Clients Nationwide
100%
Commitment to Quality

Frequently Asked Questions

What is CQV?

CQV stands for Commissioning, Qualification, and Validation. It is a structured process used in the pharmaceutical and biotech industries to ensure that facilities, equipment, and systems perform as intended and meet regulatory requirements.

Do you serve clients outside of Connecticut?

Yes, Salent Solutions serves clients nationwide. While our headquarters is in Brookfield, CT, our team supports projects across the United States.

Can you support urgent or fast-tracked projects?

Absolutely. We specialize in managing complex, fast-paced projects, including those executed under tight timelines or during challenging conditions such as the pandemic.

What industries do you serve?

We primarily serve the biotechnology and pharmaceutical industries, supporting companies that develop and manufacture life-saving and life-altering therapies.

How do I get in touch for a project inquiry?

You can reach out through the official website to discuss your project needs. We respond promptly to all inquiries.

Get in Touch

Contact us to learn more about Salent’s services and how we can support your pharmaceutical or biotechnology project.

Location: Serving clients nationwide. HQ in Brookfield, CT.

Visit Official Website

For job opportunities, please visit the official site to submit your resume. We’re always looking for exceptional talent to join our mission.

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