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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 …
SẢN PHẨM THUỐC
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.
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.
Liên hệ chúng tôiPHÂN TÍCH SẢN PHẨM THUỐC
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An extensive set of analytical testing and acceptance criteria is applicable to drug products –including universal and specific test criteria established by ICH …
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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