- Homepage
- About us
Who we are
Defined by Trust.
Founded in 2016 by Vinod Borsadiya, Sanjay Patel, Mukund Patel, and Akash Patel, PLS Analytical was established with a clear vision: to be more than a testing vendor by serving as a trusted scientific partner to pharmaceutical manufacturers and CDMOs. Beginning with analytical testing, we expanded into microbiology, nasal testing, and other specialized capabilities in response to the evolving needs of our clients.
Today, PLS Analytical supports pharmaceutical, biotech, nutraceutical, medical device, cosmetic, dietary supplement, food, and healthcare companies through integrated analytical chemistry, microbiology, manufacturing support, and scientific consulting services. Operating from our FDA-inspected, DEA-registered, cGMP-compliant facility in East Brunswick, New Jersey, our experienced scientists combine scientific expertise, advanced technology, and robust quality systems to deliver accurate, regulatory-ready results.
Nearly a decade of partnering with leading pharmaceutical companies and CDMOs has provided deep experience across every stage of the product lifecycle. Building on this foundation, PLS has evolved beyond contract testing to offer integrated Contract Development and Manufacturing (CDMO) solutions, bringing development, testing, manufacturing, packaging, and regulatory support together under one roof. We built this company to serve as the behind-the-scenes partner that helps great products reach patients safely and on time. That mission hasn't changed, but our vision has grown.
Mission
To be the most trusted analytical testing partner in the pharmaceutical industry, delivering scientific rigor, regulatory confidence, and unwavering quality at every stage of our clients' product journey.
Vision
To evolve from the industry's most reliable Contract Testing partner into a comprehensive Contract Development and Manufacturing Organization, becoming the single partner pharmaceutical, biotech, and nutraceutical companies turn from concept to commercialization.

Quality Assurance
Data Integrity
Regulatory & Lifecycle Support/ Lifecycle Partnership
Validated Processes
Regulatory Alignment (FDA-Approved, cGMP Compliance, DEA-Registered)
Benefits of outsourcing
Faster execution and scalable support
Access to specialized expertise & infrastructure
Regulatory & quality-focused operations
Operational efficiency & resource optimization
Focus on core business priorities
Integrated end-to-end support
Timeline
Message from Our CEO
Leadership
Contact Us
Connect with our scientific and operational teams to discuss testing, manufacturing, packaging, or regulatory support requirements.
Address
40E Cotters Lane, Suite A, East Brunswick, NJ-08816






