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Non‐Biological Complex Drugs/
Guidelines

Liposome V15L11

FDA issues final guidance on liposome drug products

Non‐Biological Complex Drugs/Guidelines | Posted 27/04/2018

On 4 April 2018, the US Food and Drug Administration (FDA) issued a new draft guidance document for non-biological complex drugs (NBCDs). The finalized guidance covers what applicants should submit for new drug applications (NDAs) and abbreviated new drug applications (ANDAs) for liposome products.

NBCD 1 V13J25

US guidelines for follow-on NBCDs

Non‐Biological Complex Drugs/Guidelines | Posted 10/06/2016

Last update: 1 June 2018

The regulatory body for approval of medicines in the US is the Food and Drug Administration (FDA).

Guidance V13F21

FDA includes follow-on versions in its new cyclosporine guideline

Non‐Biological Complex Drugs/Guidelines | Posted 29/04/2016

In February 2016, the US Food and Drug Administration (FDA) issued a new draft guidance document for non-biological complex drugs (NBCDs). The new draft guidance on cyclosporine drug products replaces draft guidance published in March 2015.

Liposome V15L11

FDA includes follow-on versions in its new liposome guideline

Non‐Biological Complex Drugs/Guidelines | Posted 26/02/2016

On 29 October 2015, the US Food and Drug Administration (FDA) issued a new draft guidance document for non-biological complex drugs (NBCDs). The new draft guidance on liposome drug products replaces draft guidance published in August 2002.

EMA logo 1 V13C15

EU guidelines for follow-on NBCDs

Non‐Biological Complex Drugs/Guidelines | Posted 22/01/2016

Last update: 22 January 2016

The regulatory body for approval of medicines in the European Union (EU) is the European Medicines Agency (EMA). The agency is responsible for the scientific evaluation of medicines developed by pharmaceutical companies for use in the EU.

24-AA011041

EMA issues reflection paper for follow-on versions of iron-based nano-colloidal products

Non‐Biological Complex Drugs/Guidelines | Posted 05/11/2015

On 27 March 2015, the European Medicines Agency (EMA) published its reflection paper for follow-on versions of iron-based nano-colloidal products. The agency first released the draft reflection paper for follow-on versions of iron-based nano-colloidal products for a three-month consultation period in September 2013.