Medicines and Healthcare products Regulatory Agency

Issued following an inspection in accordance with :

Regulation 5 of the current Veterinary Medicines Regulations

  The competent authority of United Kingdom confirms the following :    

Has been inspected under the national inspection programme in connection with manufacturing authorisation no. UK ManA 18756 in accordance with Regulation 5 of The current Veterinary Medicines Regulations

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 04/12/2020, it is considered that it complies with

• The principles and guidelines of Good Manufacturing Practice laid down in Regulation 5 of the current Veterinary Medicines Regulations

This certificate reflects the status of the manufacturing site at the time of the inspection noted above and should not be relied upon to reflect the compliance status if more than three years have elapsed since the date of that inspection. However, this period of validity may be reduced or extended using regulatory risk management principles by an entry in the Restrictions or Clarifying remarks field. This certificate is valid only when presented with all pages and both Parts 1 and 2. The authenticity of this certificate may be verified in MHRA-GMDP. If it does not appear, please contact the issuing authority.

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Operations

1. MANUFACTURING OPERATIONS

[ 1.5 ] Packaging

[ 1.5.1 ] Primary packaging

[ 1.5.1.1 ] Capsules, hard shell

[ 1.5.1.2 ] Capsules, soft shell

[ 1.5.1.4 ] Impregnated matrices

[ 1.5.1.8 ] Other solid dosage forms

[ 1.5.1.12 ] Suppositories

[ 1.5.1.13 ] Tablets

[ 1.5.1.14 ] Transdermal patches

[ 1.5.1.15 ] Intraruminal devices

[ 1.5.2 ] Secondary packaging

Contact Details

20/10/2021	Name and signature of the authorised person of the Competent Authority of United Kingdom
	Confidential
	Medicines and Healthcare products Regulatory Agency
	Tel : Confidential