regaffairs_find_pharma_gmp_and_ich_guidance

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Finds what a GMP or ICH guideline requires and the text of a GMP annex or ICH guideline, and checks whether a UK site holds an MHRA manufacturing or wholesale (GMP/GDP) licence. It covers EU GMP (EudraLex Volume 4, Parts I to IV and Annexes 1 to 21), US cGMP for finished pharmaceuticals (21 CFR Parts 210 and 211), the ICH Quality, Safety, Efficacy and Multidisciplinary guidelines and the ICH M4 Common Technical Document, Directive 2001/83/EC, the MHRA GMDP register (GMP and GDP certificates, manufacturer and wholesaler authorisations), MHRA GMP inspection deficiency data, and EDQM OMCL network market surveillance reports. It returns passages with the guideline code, section and version date. Give a topic, a guideline code or a site or company. It does not count as a question. Not intended for whether a medicine is authorised or in shortage (`regaffairs_check_drug_or_device_approval` covers that), for clinical trial conduct or GCP, or for FDA submission strategy.