CDFormulation:PharmaceuticalAnalysisBringsMore ConfidencetoDrugDevelopmentandGMPManufacturing
EquippedwithacGMP-compliantlaboratoryandstate-of-the-art analyticalinstruments,CDFormulation’sseasonedresearchteamis well-preparedtohandlethemostcomplicateddruganalyticalissues asacontractserviceorganization.Thesamplestobetestedand analyzedcouldbeintheformofsolids,semi-solids,liquids,orgases.
Inbrief,pharmaceuticalanalysisinvolvesaseriesofprocesses, includingidentification,determination,quantitation,andpurification. Throughoutthisprocess,qualitativeanalysisandquantitative analysisarethetwomostfrequentlyusedanalyticalmethods.
“Inthebeginning,peoplemayviewpharmaceuticalanalysisas analyticalchemistrydealingwithdrugsubstancesandpharmaceutical products,butinfact,analyticalchemistsareinvolvedinmanymore studies,includingtheanalysisofthechiralpurityandqualityof pharmaceuticalformulations,drugqualitycontrolaswellas pharmacokineticstudies,”theMarketingChiefofCDFormulation revealed.
Morespecifically,CDFormulationiscapableofconductingthe followingpharmaceuticalanalysisservices.
AnalysisandTestingServices
Takingadvantageofitsextensivetechnicalexpertiseinbiochemistry, molecularandcellbiology,chemistry,andmicrobiology,CD Formulationcanprovidecomprehensive,innovative,andtimely solutionstohelpcustomersquicklycompletetheirdruganalysis testingrequirements.Therangeofanalyticaltestingmainlycovers physicalparameterdetermination,biologicaldetermination,impurity determination,propertydetermination,andstabilityanalysis.
AnalyticalMethodologyResearchServices
Analyticalmethodsmustbeverifiedfirstbeforeusetoensurethe correctness,scientificity,integrityandfeasibilityofanalyticaltest results.CDFormulationprovidesmethoddevelopmentandvalidation services,includingmethoddevelopmenttrialdesign,processreports, validationmethodsandvalidationreports,analyticalassaysforAPIs anddrugformulations,forstabilitycontentstudiesorrelated substances.Duringthisprocess,awiderangeofchromatographic (HPLC,UPLC,GC,IC),spectroscopic(ICP,AAS,AS,AFS)and
detectiontechniques(UV,MS,IR,FID,ECD,etc.)areemployedto meetdifferenttypesofservices.
PrescriptionScreeningProcessAnalysis
Systematicpre-formulationstudieswilleffectivelyguidethedesignof clinicalformulationsofdrugsandthedevelopmentofsafe,effective, stable,controlled,andeasy-to-useformulations.Owingtoitsstrong hardwareandtechnicalcapabilitiesinthefieldofpre-formulation analysis,CDFormulationcanprovideafullrangeofpre-formulation services,includingAPIPhysical&ChemicalCharacterization,Solid StateCharacterizationofAPIs,DissolutionRateTest,Solubility Analysis,AdhesionTest,CrystallinityDetermination,ParticleSize Analysis,PowderFlowabilityTest,DeterminationofContactAngleof PharmaceuticalExcipients,ConePenetrationTest,SolidDensityTest, BulkDensityandCompactionDensityTest,TabletHardnessTest, AmorphousContentDetermination,HygroscopicityEvaluation,and API-ExcipientCompatibility.
Please visit the website https://www.formulationbio.com/analytical.htmltoexploremoreof CDFormulation’spharmaceuticalanalysiscapabilities.
About
Knownforitsrobustexpertiseandprofoundprofessionalism,CD Formulationisawell-chosenpartnerforpharmaceuticalcompaniesto solvedrugformulation-relatedchallenges.Meanwhile,afullrangeof excipients,cosmeticingredients,andfoodingredientsarenowalso availableatCDFormulation.