PerkinElmer

Drug Product

Mitigating risk while maximizing production

Drug product or finished dosage form (tablet, capsule, injectables) contain a drug substance (API) and excipients. All drug products must be GMP compliant to be released for commercial use.

The suitability of a drug product for its intended use is defined by attributes such as the identity, strength, and purity – which can be achieved by using instruments, consumables and services you can find from PerkinElmer.

Our analytical instrumentation, informatics solutions, and service and support, provide pharmaceutical manufacturers confidence in the quality of their product and compliance in their process from beginning to end.

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Extractables & Leachables

Pharmaceutical laboratories must evaluate the interactions between packaging material and formulation, applying risk assessments defined on ICH Q9 guidelines to ...

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Drug Product Assay

An extensive set of analytical testing and acceptance criteria is applicable to drug products –including universal and specific test criteria established by ICH ...

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Primary Packaging

GMP accredited labs check the quality of primary packaging containing drug products. The testing and qualification of plastic packaging systems and components f ...

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Content Uniformity Made Easy

Content uniformity is an essential quality measure during the production of finished dosage forms and requires the best blend uniformity, which is particularly ...

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Dissolution Testing

Pharmaceutical labs consider dissolution testing to be one of the critical steps in the drug development process. It makes an impact at almost every step of the ...

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Elemental Impurities Testing

Elemental Impurities in drug products can arise from several sources, including interactions with processing equipment or container/closure systems, presence in ...

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