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CEP holders invited to comment on draft monographs published in Pharmeuropa 33.2

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21 April 2021
Strasbourg, France

CEP holders are requested to consult the list of substances for which draft revised monographs of the European Pharmacopoeia (Ph. Eur.) have been published in Pharmeuropa 33.2. The table below lists the substances affected by these revisions and for which a certificate of suitability to the Ph. Eur. monographs (CEP) has been granted.

Users are encouraged to register for free, giving them access to Pharmeuropa on the European Directorate for the Quality of Medicines & HealthCare (EDQM) website Pharmeuropa, Pharmeuropa Bio & Scientific Notes.

Although these draft monographs are published for public consultation only at this stage and are therefore not official standards, they will, once adopted by the European Pharmacopoeia Commission, become legally binding standards for the substances concerned. It is therefore extremely important that manufacturers and users of the substances provide feedback on these draft monographs before the commenting deadline, i.e. before 30 June 2021. Comments made after adoption of a monograph and/or the publication in the Ph. Eur. will not be considered and manufacturers and users of substances concerned may find themselves in a position where their substance does not comply with the relevant Ph. Eur. monograph, which is a legal standard in Europe.

Everyone benefits from European Pharmacopoeia monographs which reflect the quality of the substances available in Europe. The EDQM therefore strongly encourages all users of CEPs for which a draft revised monograph has been published to review the draft monographs and check whether their substance complies with the revised draft.

Feedback on a draft monograph may be submitted in different ways, depending on where your company is located:

  • for companies located in a European Pharmacopoeia member state, please send comments through the relevant National Pharmacopoeia Authority;
  • for companies located in a country which is not European Pharmacopoeia member state, please send comments directly using the EDQM HelpDesk (topic 04-European Pharmacopoeia & International Harmonisation).

Please consult the guide “How to comment” for more information.

Comments on draft monographs should NOT be sent directly to the Certification of Substances Department.

Calcium pantothenate – 0470

Carprofen for veterinary use – 2201

Ciprofibrate – 2013

Dequalinium chloride hydrate – 1413

Dihydrostreptomycin sulfate for veterinary use – 0485

Enrofloxacin for veterinary use – 2229

Everolimus – 2918

Febantel for veterinary use – 2176

Fenbendazole for veterinary use – 1208

Flunarizine dihydrochloride – 1722

Glucose – 0177

Glucose monohydrate – 0178

Isradipine – 2110

Marbofloxacin for veterinary use – 2233

Mefloquine hydrochloride – 1241

Moxidectin for veterinary use – 1656

Pimobendan for veterinary use – 2179

Selamectin for veterinary use – 2268

Theophylline-ethylenediamine – 0300

Theophylline-ethylenediamine hydrate – 0301

Xylazine hydrochloride for veterinary use – 1481

See also:

 

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