Coriolis Cor-Competences® (Accelerator Analytical Platforms)

Advance your analytical program with our standardized and rapidly deployable accelerator analytical platform services (Coriolis Cor-Competences®), purpose built to streamline decision making and reduce analytical uncertainties early in development. All platforms follow a consistent, high quality framework whenever the molecule fits into the platform, which is set-up to cover a broad range of relevant biologics. For all other molecule types, we provide dedicated bespoke development to ensure the most suitable analytical pathway.

Your Benefits with Analytical Platforms

At Coriolis Pharma, we combine deep scientific expertise with one of the largest portfolios of analytical services in biopharmaceutics. After years of supporting clients across proteins, mAbs, peptides, AAV and many other modalities, we are proud to introduce our Analytical Platform Services — designed for speed, simplicity, and scientific reliability.

 

Configure your project in minutes

Pick exactly what you need:

• Your preferred analytical methods
• Number of samples
• Reporting depth (tabulated summary or full scientific report)
• Turnaround time — from 1 week (super urgent) to 6 weeks (relaxed), with transparent pricing tiers

Find the perfect balance between speed and budget.

50 in-house analytical methods, instantly available

We offer a robust suite of ~50 standardized, inhouse methods that are fully documented and ready for immediate sample testing. No method development. No optimization phase. Just rapid, reliable analytics from day one.

Fast contracting, zero friction

All projects run under our Standard Terms — meaning no lengthy legal negotiations. You get a short proposal, confirm, and we start immediately.

Smooth logistics and predictable delivery

Send your samples (plus MSDS), and you will receive your report within the selected TAT. Simple. Efficient. Reliable.

GRP-Compliant Service

You receive high quality scientific data generated under our strict GRP framework — ensuring consistency, traceability, and trust.

Need more than standardized methods?

Our well established Tailored Analytical Services remain fully available. If your molecule requires custom method development, deeper scientific consultation, or specialized study design, our experts are ready to work with you — before, during, and after the project.

Discover Accelerator Development Platforms

Analytical Method Development, Qualification and Validation

For common sample types, we can often apply standardized methods with little setup effort. However, when needed, our experienced analytical experts create or optimize custom methods tailored to your active pharmaceutical ingredient, product type and development phase.

Method Development

Our method development approach tailors sample preparation, method settings and data analysis to the needs of your project and sample.

We include representative samples and, where available, suitable reference standards and stressed/degraded materials, allowing our analytical scientists to design a highly suitable, stability-indicating, robust and repeatable method. Upon request, we will compile a detailed description of the method for your records.

Method Qualification

Method qualification is the initial assessment of an analytical procedure’s performance to show its suitability for its intended purpose.

During method qualification, our analytical scientists perform documented testing demonstrating that the analytical procedure meets criteria in several categories. Criteria may include factors such as repeatability, specificity and robustness. We compile a qualification plan and report, including all relevant data.

Method Validation

Under GMP conditions, method validation confirms that an analytical procedure’s performance suits its intended purpose. Depending on the method’s scope, a broad range of method characteristics, such as specificity, accuracy, precision, limit of detection/limit of quantification (LOD/LOQ), linearity and range, is considered.

During method validation, our analytical scientists perform documented testing demonstrating that the analytical procedure consistently produces a result that meets the predetermined acceptance criteria. We compile a validation plan and report that includes all relevant data.

Depending on the development phase, a fit-for-purpose validation approach can be offered, adjusting the validation required efforts in a phase-appropriate way to meet the method’s needs.

Method Verification

Compendial method verification confirms that a compendial method (e.g., from Ph. Eur. or USP) is suitable and reliable for its intended purpose under the specific conditions of the laboratory.

Unlike full method validation, compendial method verification is often considered a partial validation since the method has already undergone extensive testing and validation during its inclusion in the compendium. The extent of method verification depends on the type of method.

During method verification, our analytical scientists perform documented testing demonstrating that the developed analytical method performs adequately for the specific product or matrix being tested and within the specific laboratory where the method will be employed.

We’ve worked with over 980 biotherapeutics and the number is growing by the day.

Analytical Platforms for Your Drug Product

Coriolis Pharma’s deep expertise across many biologic modalities, combined with input from world-leading external advisors, offers the knowledge and experience needed to solve even the most complex formulation and drug development challenges.

Your Phase

Our expert team has the expertise and experience to guide your biopharmaceutical development program from preclinical and early-phase development to the market.

Coriolis Effect

See how our expertise and comprehensive services accelerate biologics development from preclinical to the market.

Analytical Platform Resources

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Talk to Our Experts or Request a Quote

Our expert team is ready to answer your questions and guide you to the services best suited to your program’s modality, stage and challenge. If your needs are well-defined, we’ll begin the quotation process.

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Driving Success 
from Preclinical to Commercial Approval & Beyond

A guide for early and late-stage development, commercialization, and lifecycle management

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