ToaddanewsectiontotheICHQ7guideline(GoodManufacturingPracticeforActivePharmaceuticalIngredients),youcanfollowthisexampleinplaintextformat:NewSection:[SectionNumberandTitle][Providethenewsectiontitlehere,e.g.,"X.YNewAspectofAPIManufacturing"][Insertthecompletetextofthenewsectionhereinclear,regulatory-stylelanguage.ThecontentshouldbeconsistentwiththeexistingQ7structureandprinciples,focusingonGMPaspectsforAPIs.Includeanynecessarydefinitions,requirements,orrecommendationsasappropriate.][Ifapplicable,addanycross-referencestootherrelevantICHguidelinesorregulatorydocuments.][Endwithaclearstatementthatcompletesthesection,maintainingconsistencywiththerestofthedocument.]Forexample,ifaddingasectiononcontinuousmanufacturing:"X.YContinuousManufacturingofAPIsThissectionappliestothecontinuousmanufacturingofactivepharmaceuticalingredients...[detailedcontent]...RefertoICHQ13foradditionalguidanceoncontinuousmanufacturingapproaches.TheprinciplesofthissectionshouldbeappliedinconjunctionwithotherrelevantsectionsofICHQ7."WouldyoulikemetoprovidemorespecificcontentforaparticulartopicyouwanttoaddtoICHQ7?Pleasespecifythesubjectmatteryouwishtoinclude.
