Age-related macular degeneration (AMD) is a chronic condition that is one of the leading causes of irreversible blindness in people over 50 years of age. AMD is the most common cause of vision loss in the western world, and globally is the third most common cause after cataracts and glaucoma. In 2002, the World Health Organization reported that AMD accounted for 8.7% of the 37 million cases of blindness worldwide—over 3.2 million cases.1 AMD is classified into two forms: non-exudative (‘dry') AMD and exudative (‘wet') AMD. With dry AMD, cellular debris accumulates between the retina and the choroid, which contains the blood vessels that supply nourishment to the retina, particularly the macula (central retina). This results in atrophy of the retina and the underlying pigment epithelial layer, causing slow and progressive loss of vision. Wet AMD is far more severe and may develop de novo or from pre-existing dry AMD. In wet AMD, new blood vessels also begin to grow from the choroid (choroidal neovascularization; CNV). Bleeding, leaking, and scarring caused by these blood vessels distorts and blurs the central vision: with time, the bleeding, fluid leakage, and subsequent scar formation damages the retina, and can eventually lead to severe vision loss or blindness. Although wet AMD is the less common form, occurring in 10–15% of cases, it accounts for ∼80–90% of AMD-associated severe visual loss.2 Before the development of the first treatment for wet AMD, predominantly classic CNV usually led to permanent and almost complete central vision loss within 3–6 months of diagnosis.3 The first approved pharmacological treatment of wet AMD was verteporfin (Visudyne, Novartis Pharma AG, Basel, Switzerland) in 2001, a light-activated drug for use in photodynamic therapy (PDT).4 In 2004 and 2006, respectively, the vascular endothelial growth factor (VEGF) inhibitors pegaptanib (Macugen, Gilead Sciences, Foster City, CA, USA and Pfizer Inc., New York City, NY, USA) and ranibizumab (Lucentis, Genentech Inc., San Francisco, CA, USA and Novartis) were licensed by the US Food and Drug Administration (FDA) for the treatment of wet AMD.5, 6 On the basis of the results of several clinical trials (Table 1), ranibizumab is currently considered the gold-standard of care for wet AMD as reported by the UK Royal College of Ophthalmologists,7 and has been endorsed by other professional societies and associations (eg, the Swiss VitreoRetinal Group8) as well as the UK National Institute for Health and Clinical Excellence (NICE).9 Table 1 Common clinical issues and concerns Ranibizumab is a therapeutic antibody fragment that binds to human VEGF-A isoforms and prevents receptor binding. VEGF is a regulator of normal and abnormal angiogenesis, and intraocular VEGF levels correlate with blood vessel formation or increased vascular permeability in a number of retinal disorders, including wet AMD.10 By blocking the action of VEGF, ranibizumab can prevent and reverse vision loss caused by wet AMD-associated CNV.11 Ranibizumab was specifically developed for application in ophthalmology from murine anti-VEGF antibody A.4.6.1.12 and is specifically manufactured according to US Pharmacopeia specifications for injections into the eye.13, 14 This ensures it has fewer particulates compared with products developed for intravenous use, and thus a putatively lower potential for ocular irritation and inflammation.15 Ranibizumab is manufactured as a 10 mg/ml solution in single-use vials containing 0.2 ml of ranibizumab.6 To be effective, 0.05 ml of the solution (0.5 mg ranibizumab) must be injected directly into the vitreous humour of the eye. This is an invasive and specialized procedure, which differs from typical cutaneous and intramuscular injections in several important ways. First, the eye is an immunopriviledged, delicate, and important sensory organ and as such the procedure requires a very high level of sterility and precision.6 Second, unlike some injections such as insulin administration in diabetic patients, ranibizumab injections cannot be self-administered. Because of the delicate location of the injection, and the expertise required to avoid or address any severe complications that may occur (including retinal detachment, traumatic cataracts, and endophthalmitis), they must be performed by a qualified ophthalmologist experienced in intravitreal injections.16 Third, full aseptic technique should be adhered to at all times, including the use of a clean room or operating theatre and surgically sterile equipment.6, 16, 17 Lastly, appropriate anaesthesia and broad-spectrum microbicides are required before the procedure, and afterwards essential monitoring for infection, inflammation, and other complications requires specialized medical equipment, such as a tonometer or biomicroscope.6 For these reasons, the intravitreal injection of ranibizumab, or indeed any intravitreal injection, is considered a surgical procedure. As such, although ranibizumab is a drug, it can only be administered by intravitreal injection for the treatment of wet AMD-associated CNV. It should therefore be considered both a surgical and medical treatment, and should be subject to healthcare regulations and reimbursement appropriate to both classifications. Additional issues are addressed in Table 1. The author is Vice President of the Royal College of Ophthalmologists (London) and Chairman of its Scientific Committee (whose duties include assessing the impact of new intravitreal injections and other AMD treatments in the British National Health Service). He is also Associate Professor at the University of Nottingham and Honorary Consultant Ophthalmic Surgeon at Queen's Medical Centre University Hospital, Nottingham, UK. In his professional opinion, ranibizumab is a drug therapy. However, it needs to be administered through a surgical procedure undertaken by clinicians experienced in such procedures, that is, a trained ophthalmologist. This is because the procedure is potentially dangerous and can result in permanent loss of eyesight.18 One example is the sudden occlusion of optic nerve head perfusion, which if not treated within 3 min can result in permanent vision loss.18 Other serious risks include traumatic cataracts, retinal detachments, and acute endophthalmitis.19 In conclusion, ranibizumab is a pharmacological treatment that can only be delivered via a surgical procedure, which requires a trained specialist, cannot be self-administered, and should be performed in a clean room or operating theatre with sterile equipment. Ranibizumab should therefore be considered both a medical and surgical treatment, and should be subject to healthcare regulations and reimbursement appropriate to both classifications.