Medicines and Healthcare products Regulatory Agency

CERTIFICATE NUMBER : UK API 12822 Insp GMP/GDP 12822/3399-0001 [V]

Certificate of GMP Compliance Of A Manufacturer(1),(2)

Part 1
Issued following an inspection in accordance with :

Regulation 5 of the current Veterinary Medicines Regulations

  The competent authority of United Kingdom confirms the following :
The Manufacturer : F D COPELAND AND SONS LIMITED
 
Site address : F D COPELAND AND SONS LIMITED, COLANOL HOUSE, 5 WESTFIELD STREET, LONDON, SE18 5TL, UNITED KINGDOM
 

Is an active substance manufacturer that has been inspected in accordance with Regulation 327 of The Human Medicines Regulations 2012 (SI 2012/1916).

From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 10/09/2019, it is considered that it complies with

  • The principles of GMP for active substances referred to in Regulation B17 and C17 of the Human Medicines Regulations 2012 (SI 2012/1916)

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.


  • (1) Guidance on the interpretation of this template can be found in the Help menu of MHRA-GMDP database.
  • (2) These requirements fulfil the GMP recommendations of WHO.
Part 2
Veterinary Medicinal Products

Manufacture of active substance. Names of substances subject to inspection:

  • [4000010071] PEPPERMINT OIL
  • [2000007590] EUCALYPTUS OIL
  • [4000009155] DEMENTHOLISED MINT OIL
  • [4000015351] CAJEPUT OIL
  • [4000010430] CLOVE OIL
  • [4000007306] JUNIPER BERRY OIL
Active Substances
3. MANUFACTURING OPERATIONS - ACTIVE SUBSTANCES
PEPPERMINT OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
vacuum distillation
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

EUCALYPTUS OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
vacuum distillation
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

DEMENTHOLISED MINT OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
vacuum distillation, filtration
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

CAJEPUT OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
Vacuum distillation
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

CLOVE OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
vacuum distillation
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

JUNIPER BERRY OIL
3.2Processing Activities of Active Substance from Natural Sources
3.2.1  Plant Source Extraction

3.2.6  Purification of extracted substance

3.5General Finishing Steps
3.5.1  Physical Processing Steps
vacuum distillation
3.5.2  Primary Packaging

3.5.3  Secondary Packaging

3.6Quality Control Testing
3.6.1  Physical / Chemical testing

Contact Details
29/10/2019 Name and signature of the authorised person of the Competent Authority of United Kingdom
Confidential
Medicines and Healthcare products Regulatory Agency
Tel : Confidential