Restrictions On The Import Of Unlicensed Melatonin Products Following The Grant Of A Marketing Authorisation For Circadin(R) 2mg Tablets

Main Category: Pharma Industry / Biotech Industry
Article Date: 19 Aug 2008 - 0:00 PDT

email icon email to a friend   printer icon printer friendly   write icon opinions  

Current Article Ratings:

Patient / Public:not yet rated

Healthcare Prof:not yet rated


Dear Healthcare Professional,

Restrictions on the import of unlicensed Melatonin products following the grant of a marketing authorisation for Circadin® 2mg tablets

At the beginning of June 2008, a licensed modified release melatonin product, Circadin ® (Lundbeck), became available in the UK.

Before June 2008, melatonin was only available in the UK in unlicensed medicinal products, many of which were non-pharmaceutical grade products imported from the United States of America, where melatonin products are classed as supplements, not medicines. These products are not required to be manufactured to the standards of Good Manufacturing Practice normal for pharmaceuticals. It is therefore important to ensure that the licensed product available in the UK is used wherever possible. This includes off-label use of the licensed product , if deemed suitable by the clinician.

It is recognised, however, that there may be individual patients for whom the UK product cannot meet their clinical needs. In particular, there may be some need for alternative dosage forms, or strengths, or for an immediate release product.

Importation of unlicensed melatonin products remains possible under the MHRA scheme for the import of unlicensed medicines. Details of the scheme are available in our Importing unlicensed medicines section.

Prescribers will need to provide written details of the special clinical need to the importer for submission to the MHRA. Details have to be provided with every order and not just the first occasion.

Patient identification is not required in letters from clinicians in order to maintain patient confidentiality.

The MHRA does not provide template letters for clinicians. Importers are familiar with the MHRA requirements for letters concerning special clinical need. For questions on this area we would ask any newly affected parties to contact their proposed importer in the first instance. For all other enquiries on this notice, please contact Ms Raia Stoyanova on 0207 084 2625.

Primary Care Trusts are requested to forward this letter to General Practitioners and Retail Pharmacies. NHS QC recipients are requested to forward this to Purchasing Pharmacists and Clinicians.

Yours faithfully

Ian Holloway
MHRA DMRC Manager

http://www.mhra.gov.uk

Article adapted by Medical News Today from original press release.
Visit our pharma industry / biotech industry section for the latest news on this subject.
There are no references listed for this article.
Please use one of the following formats to cite this article in your essay, paper or report:

MLA
MHRA. "Restrictions On The Import Of Unlicensed Melatonin Products Following The Grant Of A Marketing Authorisation For Circadin(R) 2mg Tablets." Medical News Today. MediLexicon, Intl., 19 Aug. 2008. Web.
14 Feb. 2012. <http://www.medicalnewstoday.com/releases/118567.php>

APA
MHRA. (2008, August 19). "Restrictions On The Import Of Unlicensed Melatonin Products Following The Grant Of A Marketing Authorisation For Circadin(R) 2mg Tablets." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/118567.php.

Please note: If no author information is provided, the source is cited instead.


Pharma Industry / Biotech Industry

Most Popular Articles



Follow Our Pharma Industry News On Twitter

Follow Us On Twitter
Get the latest news for this category delivered straight to your Twitter account. Simply visit our Pharma Industry / Biotech Industry Twitter account and select the 'follow' option.



View list of all 'What Is...' articles »