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Your Pharmaceutical Testing Partner.

A GMP pharmaceutical testing laboratory delivering quality results, dependable execution, and responsive project support.
Tentamus Pharmaceuticals Sciences is part of the Tentamus Group
Services
We combine the technical horsepower of a global network with the agility of a dedicated partner. Whether you need a complex method validation or routine release testing, we deliver reliability you can trust.
Quality & Compliance
Compliance isn't a department here; it's our product. We operate under a rigorous Quality Management System (QMS) designed to withstand the scrutiny of the world's toughest regulatory bodies.
Resources
The regulatory landscape is constantly shifting. We provide the technical insights and regulatory updates you need to keep your products compliant and your patients safe.

Tentamus
Pharmaceutical Sciences

Tentamus Pharmaceutical Sciences provides a comprehensive range of analytical, microbiological, and regulatory support services tailored to the pharmaceutical and biopharmaceutical industries. As part of the global Tentamus Group, we combine deep scientific expertise with a connected network of specialized laboratories to deliver reliable, high-quality data that supports product safety, quality, and compliance.

Our services span method development and validation, stability studies, microbiology testing, and advanced analytical solutions designed to meet evolving regulatory requirements. We work closely with our clients to streamline testing workflows, reduce risk, and ensure confidence at every stage of the product lifecycle.

  • Method Development & Validation

    From forced degradation to full ICH guideline adherence, we handle the complex protocols that ensure your methods are robust.

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    method

  • Analytical Chemistry

    Comprehensive testing including Assay, Impurities, Dissolution, and Elemental Impurities using state-of-the-art ICP-MS.

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    chemistry

  • Microbiology & Sterility

    Full suite of USP <61>, <62>, and <71> testing, including Endotoxin, Bioburden, and Preservative Efficacy (AET).

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    microbio

  • Stability & Storage

    Network-backed stability storage managing standard ICH conditions (25C/60%RH, 30C/65%RH, 40C/75%RH) for shelf-life efficacy.

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    storage

  • Raw Materials

    Supply chain integrity starts with raw materials. We offer full monograph testing for excipients and APIs, ensuring your inputs meet the strictest global standards.

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    raw
audit

Audit-Ready. Every Day.

We operate under a strict Quality Management System (QMS) designed to meet 21 CFR Part 11 requirements. Our LIMS ensures secure role-based access, audit trails, and data integrity from sample receipt to COA generation.

Need to sign a Quality Agreement? We make onboarding seamless so you can start testing immediately.

View Our Quality & Compliance
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