Guide to Wholesaling & Brokering of Medicinal Products - Ireland
Guidance on Requirements for Import / Re-export Medical Imaging Materials - SFDA
Guide on Microplastic Usage - IPEC Europe and IPEC-Americas "How to Document"
EMA Guidance on Post-Authorisation Procedural Advice for CAP users & EudraVigilance Reg. Manual
USFDA's recent Guidance on Biologics: Ophthalmic Products & Development of (CAR) T Cell Products
EMA Guidance on GVP for PPP & Parallel EMA/EUnetHTA 21 Consultation
Guidance on Renewal & Discontinuation of Authorisation on change of Status -Swiss Medic
Malaysia Draft Medical Device Guidance on PERSONAL PROTECTIVE EQUIPMENT (PPE) - REQUIREMENTS
UK MHRA: Guidance on "Advertise your Medicines"
FDA's: OTC Monograph Drug User Fees for Fiscal Year 2022
SwissMedic Guidance on Packaging for Human Medicinal Products
USFDA Guidance on Verification Systems & Voluntary Recalls
UK (MHRA) Project Orbis Guidance Update & New Guidance on Dialysis
USFDA: 3 updated Guidance on PLAIR, VQIP & Recalls
South Africa (SAHPRA) Guidance on How to Submit Variation Applications
MHRA adds Health Technology Assessments (HTA) Tool Details to ILAP Guide